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Lignans, neolignans, and related compounds

https://doi.org/10.1039/np9951200183

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ardp.19943270309openalex-snapshot

Antineoplastic and Antiviral Activities of Podophyllotoxin Related Lignans

inferredcites →https://doi.org/10.1002/hlca.19940770318openalex-snapshot

A Novel Rearrangement Product of Podophyllotoxone – Ester Derivatives and in vitro cytotoxicity studies

inferredcites →https://doi.org/10.1002/jccs.199200076openalex-snapshot

Synthesis of (±)‐Lsodeoxypodophyllotoxin

inferredcites →https://doi.org/10.1002/mrc.1260310915openalex-snapshot

13C NMR data for several cyclolignans

inferredcites →https://doi.org/10.1002/mrc.1260311203openalex-snapshot

Complete 1H (600 MHz) and 13C NMR spectral assignments of 3,4‐bis [(3,4‐dimethoxyphenyl)‐methyl]dihydro‐(3R‐trans)‐2(3H)‐furanone (matairesinol dimethyl ether), a naturally occurring dibenzylbutyrolactone lignan

inferredcites →https://doi.org/10.1002/mrc.1260321210openalex-snapshot

Influence of skeletal alteration of lignoids on carbon‐13 NMR chemical shifts

inferredcites →https://doi.org/10.1002/rcm.1290080805openalex-snapshot

Revealing the mammalian lignan precursor secoisolariciresinol diglucoside in flax seed by ionspray mass spectrometry

inferredcites →https://doi.org/10.1002/rcm.1290081204openalex-snapshot

Investigation of mammalian lignan precursors in flax seed: First evidence of secoisolariciresinol diglucoside in two isomeric forms by liquid chromatography/mass spectrometry

inferredcites →https://doi.org/10.1007/bf00036098openalex-snapshot

Glucosylation of cyclodextrin-complexed podophyllotoxin by cell cultures of Linum flavum L.

inferredcites →https://doi.org/10.1007/bf00234715openalex-snapshot

Establishment of hairy root cultures of Linum flavum producing the lignan 5-methoxypodophyllotoxin

inferredcites →https://doi.org/10.1007/bf00686175openalex-snapshot

Cytotoxic properties of a new synthetic demethylpodophyllotoxin derivative, BN 58705, against human tumor cell lines

inferredcites →https://doi.org/10.1007/bf00993237openalex-snapshot

Magnolia virginiana Neolignan compounds as chemical barriers to swallowtail butterfly host use

inferredcites →https://doi.org/10.1007/bf01045303openalex-snapshot

Lanthanide induced shifts of aromatic 1,2,3-trimethoxy compounds: Conformational analysis of tetrahydrofurofuran-lignans in solution

inferredcites →https://doi.org/10.1007/bf01540981openalex-snapshot

Inhibition of tumor necrosis factor-alpha (TNF-?) and interleukin-1 beta (IL-1?) secretion but not IL-6 from activated human peripheral blood monocytes by a new synthetic demethylpodophyllotoxin derivative

inferredcites →https://doi.org/10.1007/bf01874092openalex-snapshot

The biotechnological production of podophyllotoxin and related cytotoxic lignans by plant cell cultures

inferredcites →https://doi.org/10.1007/bf02541548openalex-snapshot

Lignan analysis in seed oils from fourSesamum species: Comparison of different chromatographic methods

inferredcites →https://doi.org/10.1007/bf02541549openalex-snapshot

Variations in the composition of sterols, tocopherols and lignans in seed oils from fourSesamum species

inferredcites →https://doi.org/10.1016/0006-291x(89)91649-5openalex-snapshot

Topoisomerase II: A potential target for novel antifungal agents

inferredcites →https://doi.org/10.1016/0006-291x(90)90784-kopenalex-snapshot

Formation of the lignan, (−) secoisolariciresinol, by cell free extracts of Forsythia intermedia

inferredcites →https://doi.org/10.1016/0009-8981(91)90120-2openalex-snapshot

Isotope dilution gas chromatographic-mass spectrometric method for the determination of lignans and isoflavonoids in human urine, including identification of genistein

inferredcites →https://doi.org/10.1016/0021-9673(92)80321-kopenalex-snapshot

Determination of the norlignan glucosides of Hypoxidaceae by high-performance liquid chromatography

inferredcites →https://doi.org/10.1016/0024-3205(94)00641-5openalex-snapshot

Natural flavonoids and lignans are potent cytostatic agents against human leukemic HL-60 cells

inferredcites →https://doi.org/10.1016/0031-9422(83)83046-5openalex-snapshot

Neolignans from Ocotea catharinensis

inferredcites →https://doi.org/10.1016/0031-9422(83)83070-2openalex-snapshot

Biphenyls from the heartwood of taiwan sassafras

inferredcites →https://doi.org/10.1016/0031-9422(88)80780-5openalex-snapshot

Sesqui-, sester- and trilignans from stems of Cerbera manghas and C. odollam

inferredcites →https://doi.org/10.1016/0031-9422(89)80081-0openalex-snapshot

Acetylated lignans from Juniperus sabina

inferredcites →https://doi.org/10.1016/0031-9422(89)80082-2openalex-snapshot

Bicyclooctanoid neolignans from Ocotea costulatum

inferredcites →https://doi.org/10.1016/0031-9422(89)80136-0openalex-snapshot

Phenolic compounds from Coix lachryma-jobi var. Ma-yuen

inferredcites →https://doi.org/10.1016/0031-9422(89)80155-4openalex-snapshot

A lignan from Actinodaphne longifolia

inferredcites →https://doi.org/10.1016/0031-9422(89)80237-7openalex-snapshot

A biphenyl type neolignan and a biphenyl ether from Magnolia henryi

inferredcites →https://doi.org/10.1016/0031-9422(89)80367-xopenalex-snapshot

Cerberalignans J-N, oligolignans from Cerbera manghas

inferredcites →https://doi.org/10.1016/0031-9422(89)80368-1openalex-snapshot

Benzodioxane and β-aryloxy-arylpropane type neolignans from Licaria chrysophylla

inferredcites →https://doi.org/10.1016/0031-9422(89)80372-3openalex-snapshot

Pyrones and other constituents from Podolepis species

inferredcites →https://doi.org/10.1016/0031-9422(89)80393-0openalex-snapshot

Lignans from leaves of Calocedrus formosana

inferredcites →https://doi.org/10.1016/0031-9422(90)80144-6openalex-snapshot

Flavanone xyloside and lignans from Prunus jamasakura bark

inferredcites →https://doi.org/10.1016/0031-9422(90)83068-copenalex-snapshot

Sesquiterpene lactones from Tanacetum ferulaceum

inferredcites →https://doi.org/10.1016/0031-9422(90)83075-copenalex-snapshot

An aryltetralin lignan from Persea lingue

inferredcites →https://doi.org/10.1016/0031-9422(90)85020-gopenalex-snapshot

Lignoids and arylalkanones from fruits of Virola elongata

inferredcites →https://doi.org/10.1016/0031-9422(90)85025-bopenalex-snapshot

Biosynthesis of lignans in Forsythia intermedia

inferredcites →https://doi.org/10.1016/0031-9422(90)85029-fopenalex-snapshot

Production of lignans in Forsythia intermedia cell cultures

inferredcites →https://doi.org/10.1016/0031-9422(90)85050-popenalex-snapshot

Lignans of Forsythia intermedia

inferredcites →https://doi.org/10.1016/0031-9422(90)85051-gopenalex-snapshot

Three lignans from Bupleurum salicifolium

inferredcites →https://doi.org/10.1016/0031-9422(90)85052-hopenalex-snapshot

Lignans and other constituents of knema furfuracea

inferredcites →https://doi.org/10.1016/0031-9422(90)85053-iopenalex-snapshot

Neolignan glycosides from roots of Codonopsis tangshen

inferredcites →https://doi.org/10.1016/0031-9422(90)85131-xopenalex-snapshot

Flavonoids, flavonolignans and a phenylpropanoid from Onopordon corymbosum

inferredcites →https://doi.org/10.1016/0031-9422(90)85146-7openalex-snapshot

Isokaerophyllin, a butyrolactone from Bupleurum salicifolium

inferredcites →https://doi.org/10.1016/0031-9422(90)85205-topenalex-snapshot

Lignans and nor-neolignans from Krameria interior

inferredcites →https://doi.org/10.1016/0031-9422(90)85206-uopenalex-snapshot

Arylnaphthalene neolignans from Virola calophylla

inferredcites →https://doi.org/10.1016/0031-9422(90)85232-5openalex-snapshot

Dibenzocyclooctadiene lignans possessing a spirobenzofuranoid skeleton from Kadsura coccinea

inferredcites →https://doi.org/10.1016/0031-9422(90)85233-6openalex-snapshot

A neolignan from Piper sumatranum

inferredcites →https://doi.org/10.1016/0031-9422(90)85329-eopenalex-snapshot

Antioxidant activities of lignans and flavonoids

inferredcites →https://doi.org/10.1016/0031-9422(90)85460-wopenalex-snapshot

Lignans from Juniperus sabina

inferredcites →https://doi.org/10.1016/0031-9422(90)87120-jopenalex-snapshot

Lignans from Justicia hyssopifolia

inferredcites →https://doi.org/10.1016/0031-9422(90)87139-lopenalex-snapshot

Lignans from wood of Calocedrus formosana

inferredcites →https://doi.org/10.1016/0031-9422(90)89045-bopenalex-snapshot

Lignans from Aristolochia birostris

inferredcites →https://doi.org/10.1016/0031-9422(90)89073-iopenalex-snapshot

A dihydrobenzofuran lignan from Croton erythrochilus

inferredcites →https://doi.org/10.1016/0031-9422(91)80039-4openalex-snapshot

Lignans and naphthoquinones from Tabebuia incana

inferredcites →https://doi.org/10.1016/0031-9422(91)80074-bopenalex-snapshot

Podophyllotoxin related lignans in plants and cell cultures ofLinum flavum

inferredcites →https://doi.org/10.1016/0031-9422(91)80103-8openalex-snapshot

Lignans fromKrameria ixina

inferredcites →https://doi.org/10.1016/0031-9422(91)80104-9openalex-snapshot

Four neolignan ketones fromPiper capense

inferredcites →https://doi.org/10.1016/0031-9422(91)80105-aopenalex-snapshot

Phenolics from the bark ofTamarix aphylla

inferredcites →https://doi.org/10.1016/0031-9422(91)83051-lopenalex-snapshot

Lignans from polar extracts ofJuniperus thurifera

inferredcites →https://doi.org/10.1016/0031-9422(91)83052-mopenalex-snapshot

Neolignans fromAniba ferrea

inferredcites →https://doi.org/10.1016/0031-9422(91)83053-nopenalex-snapshot

Bicyclo [3.2.1] octanoid neolignans from Ocotea porosa

inferredcites →https://doi.org/10.1016/0031-9422(91)83079-zopenalex-snapshot

Neolignans fromLicaria aurea

inferredcites →https://doi.org/10.1016/0031-9422(91)83240-lopenalex-snapshot

Acidic and phenolic lignans from Juniperus sabina

inferredcites →https://doi.org/10.1016/0031-9422(91)83508-iopenalex-snapshot

(−)-di-de-o-methylgrandisin, a lignan from Virola pavonis leaves

inferredcites →https://doi.org/10.1016/0031-9422(91)83612-oopenalex-snapshot

Bioactive neolignans from the leaves of Magnolia virginiana

inferredcites →https://doi.org/10.1016/0031-9422(91)83757-copenalex-snapshot

Two diterpenoids from leaves of juniperus sabina

inferredcites →https://doi.org/10.1016/0031-9422(91)84194-wopenalex-snapshot

Matairesinol as precursor of Podophyllum lignans

inferredcites →https://doi.org/10.1016/0031-9422(91)84226-iopenalex-snapshot

Three neolignans from the roots of Piper capense

inferredcites →https://doi.org/10.1016/0031-9422(91)85061-4openalex-snapshot

Lignan and terpene glycosides from Epimedium sagittatum

inferredcites →https://doi.org/10.1016/0031-9422(91)85137-oopenalex-snapshot

A lignan and pyrone and other constituents from Hyptis capitata

inferredcites →https://doi.org/10.1016/0031-9422(91)85290-gopenalex-snapshot

Two lignans from Schisandra sphenanthera

inferredcites →https://doi.org/10.1016/0031-9422(91)85303-hopenalex-snapshot

A butyrolactone lignan disaccharide from Flacourtia ramontchi

inferredcites →https://doi.org/10.1016/0031-9422(91)85304-iopenalex-snapshot

Lignans and flavonoids from Carduus assoi

inferredcites →https://doi.org/10.1016/0031-9422(92)80008-3openalex-snapshot

Inhibition of Δ5-desaturase in polyunsaturated fatty acid biosynthesis by (−)-asarinin and (−)-epiasarinin

inferredcites →https://doi.org/10.1016/0031-9422(92)80047-iopenalex-snapshot

Kadsulignans E-G from Kadsura longipedunculata

inferredcites →https://doi.org/10.1016/0031-9422(92)80293-nopenalex-snapshot

Norlignan from the knot resin of Araucaria angustifolia

inferredcites →https://doi.org/10.1016/0031-9422(92)80295-popenalex-snapshot

Kadsulignans H, I, J and K from a Kadsura species

inferredcites →https://doi.org/10.1016/0031-9422(92)80374-nopenalex-snapshot

Isolation of secoisolariciresinol diesters from stems of Simaba cuneata

inferredcites →https://doi.org/10.1016/0031-9422(92)80485-wopenalex-snapshot

A lignan from Vitex negundo seeds

inferredcites →https://doi.org/10.1016/0031-9422(92)83111-bopenalex-snapshot

Glucosylation of butyric acid by cell suspension culture of Nicotiana plumbaginifolia

inferredcites →https://doi.org/10.1016/0031-9422(92)83137-nopenalex-snapshot

Diterpenes and a lignan from Jatropha grossidentata

inferredcites →https://doi.org/10.1016/0031-9422(92)83301-eopenalex-snapshot

Lignan glycosides from stems of Salvadora persica

inferredcites →https://doi.org/10.1016/0031-9422(92)83302-fopenalex-snapshot

Isodaurinol, an arylnaphthalene lignan from Haplophyllum cappadocicum

inferredcites →https://doi.org/10.1016/0031-9422(92)83479-iopenalex-snapshot

Three phenyldihydronaphthalene lignanamides from fruits of Cannabis sativa

inferredcites →https://doi.org/10.1016/0031-9422(92)83643-dopenalex-snapshot

Lignanolides from bupleurum salicifolium

inferredcites →https://doi.org/10.1016/0031-9422(92)83644-eopenalex-snapshot

Bicyclo[3.2.1]Octanoid neolignans from Licaria brasiliensis

inferredcites →https://doi.org/10.1016/0031-9422(92)83664-kopenalex-snapshot

A furofuran lignan from Sesamum alatum

inferredcites →https://doi.org/10.1016/0031-9422(92)83753-lopenalex-snapshot

Lignans from leaves of Juniperus chinensis

inferredcites →https://doi.org/10.1016/0031-9422(92)83756-oopenalex-snapshot

Phenolic lignans from flower buds of Magnolia fargesii

inferredcites →https://doi.org/10.1016/0031-9422(92)90049-vopenalex-snapshot

Dibenzocyclo-octadiene lignans from Kadsura heteroclita

inferredcites →https://doi.org/10.1016/0031-9422(93)85052-sopenalex-snapshot

Lignan and phenylpropanoid glycosides from Osmanthus asiaticus

inferredcites →https://doi.org/10.1016/0031-9422(93)85117-aopenalex-snapshot

Phenolics from needles of himalayan Taxus baccata

inferredcites →https://doi.org/10.1016/0031-9422(93)85150-popenalex-snapshot

Biotransformation of (+)-magnolin and (+)-yangabin in rat

inferredcites →https://doi.org/10.1016/0031-9422(93)85181-popenalex-snapshot

Lignans and a neolignan from Virola oleifera leaves

inferredcites →https://doi.org/10.1016/0031-9422(93)85182-qopenalex-snapshot

Neolignans and a phenylpropanoid glucoside from Illicium difengpi

inferredcites →https://doi.org/10.1016/0031-9422(93)85183-ropenalex-snapshot

Lignans from Trachelospermum axillare

inferredcites →https://doi.org/10.1016/0031-9422(93)85260-xopenalex-snapshot

Reassignment of structures of the neolignans, magnosalin and andamanicin

inferredcites →https://doi.org/10.1016/0031-9422(93)85367-zopenalex-snapshot

Bisbibenzyls and lignans from Pellia epiphylla

inferredcites →https://doi.org/10.1016/0031-9422(93)85368-2openalex-snapshot

Neolignans and nor-neolignans from Krameria paucifolia

inferredcites →https://doi.org/10.1016/0031-9422(93)85369-3openalex-snapshot

Cytotoxic flavonolignans and flavones from Verbascum sinaiticum leaves

inferredcites →https://doi.org/10.1016/0031-9422(93)85380-aopenalex-snapshot

3-EPI-austrobailignan-7: A 2,5-diaryl-3,4-dimethyltetrahydrofuranoid lignan from Aristolochia chilensis

inferredcites →https://doi.org/10.1016/0031-9422(93)85421-mopenalex-snapshot

Lignan glucosides from Bupleurum wenchuanense

inferredcites →https://doi.org/10.1016/0031-9422(93)85442-topenalex-snapshot

Lignans and neolignans from piperaceae

inferredcites →https://doi.org/10.1016/0031-9422(93)85452-wopenalex-snapshot

Novel benzylic ether reductions in lignan biogenesis in Forsythia intermedia

inferredcites →https://doi.org/10.1016/0040-4020(89)80041-9openalex-snapshot

Lignames

inferredcites →https://doi.org/10.1016/0040-4020(92)85007-2openalex-snapshot

Novel stereoselective synthesis of (−)-enterolactone employing chiral unsaturated lactam

inferredcites →https://doi.org/10.1016/0040-4039(91)80446-dopenalex-snapshot

A short and simple synthesis of the thioglucose analog of the antitumor agent etoposide

inferredcites →https://doi.org/10.1016/0040-4039(91)80629-kopenalex-snapshot

Facile synthesis of thioglucose analogs of the anticancer agent etoposide

inferredcites →https://doi.org/10.1016/0040-4039(94)02203-nopenalex-snapshot

Dibenzodioxocins; a novel type of linkage in softwood lignins

inferredcites →https://doi.org/10.1016/0040-4039(96)00937-9openalex-snapshot

Asymmetric total synthesis of (−) podophyllotoxin

inferredcites →https://doi.org/10.1016/0076-6879(90)87051-4openalex-snapshot

[49] Kadsurenone and other related lignans as antagonists of platelet-activating factor receptor

inferredcites →https://doi.org/10.1016/0163-7258(93)90044-eopenalex-snapshot

Podophyllotoxin, steganacin and combretastatin: Natural products that bind at the colchicine site of tubulin

inferredcites →https://doi.org/10.1016/0165-2370(91)80003-qopenalex-snapshot

Analysis of pyrolysis products of lignans using capillary gas chromatography and ion trap detection

inferredcites →https://doi.org/10.1016/0165-2370(92)85002-3openalex-snapshot

Analysis of 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octanes and dibenzylbutyrolactones by pyrolysis—gas chromatography/mass spectrometry

inferredcites →https://doi.org/10.1016/0165-2370(93)80008-nopenalex-snapshot

Pyrolysis-GC/MS of podophyllotoxin and related compounds

inferredcites →https://doi.org/10.1016/0223-5234(91)90200-7openalex-snapshot

Synthetic butanolide and tetrahydrofuran lignans with platelet activating factor antagonist activity

inferredcites →https://doi.org/10.1016/0223-5234(92)90148-topenalex-snapshot

Synthesis and antihepatotoxicity of some Wuweizisu analogues

inferredcites →https://doi.org/10.1016/0304-3835(91)90220-copenalex-snapshot

The effect of flaxseed supplementation on early risk markers for mammary carcinogenesis

inferredcites →https://doi.org/10.1016/0304-3835(94)90128-7openalex-snapshot

Gomisin A, a lignan component of Schizandora fruits, inhibits development of preneoplastic lesions in rat liver by 3′-methyl-4-dimethylamino-azobenzene

inferredcites →https://doi.org/10.1016/0957-4166(94)80161-4openalex-snapshot

Enantioselective synthesis of (R)-(+)-β-piperonyl-γ-butyrolactone

inferredcites →https://doi.org/10.1016/0960-0760(94)90030-2openalex-snapshot

Lignans and flavonoids inhibit aromatase enzyme in human preadipocytes

inferredcites →https://doi.org/10.1016/s0021-9258(18)99211-2openalex-snapshot

Formation of lignans (-)-secoisolariciresinol and (-)-matairesinol with Forsythia intermedia cell-free extracts

inferredcites →https://doi.org/10.1016/s0021-9258(19)74213-6openalex-snapshot

Stereospecificity of (+)-pinoresinol and (+)-lariciresinol reductases from Forsythia intermedia.

inferredcites →https://doi.org/10.1016/s0026-895x(25)09101-1openalex-snapshot

Podophyllotoxin analogs: effects on DNA topoisomerase II, tubulin polymerization, human tumor KB cells, and their VP-16-resistant variants.

inferredcites →https://doi.org/10.1016/s0031-9422(00)80403-3openalex-snapshot

Structural confirmation of neolignans

inferredcites →https://doi.org/10.1016/s0031-9422(00)80545-2openalex-snapshot

Randainol: a neolignan from sassafras randaiense

inferredcites →https://doi.org/10.1016/s0031-9422(00)84901-8openalex-snapshot

Lignans and neolignans from Buddleja davidii

inferredcites →https://doi.org/10.1016/s0031-9422(00)89537-0openalex-snapshot

Sesquiterpene lactones, lignans and aromatic esters from Cheirolophus species

inferredcites →https://doi.org/10.1016/s0031-9422(00)89550-3openalex-snapshot

A butyrolactone lignan dimer from Arctium lappa

inferredcites →https://doi.org/10.1016/s0031-9422(00)89582-5openalex-snapshot

Jacpaniculines the first lignanamide alkaloids from the convolvulaceae

inferredcites →https://doi.org/10.1016/s0031-9422(00)89594-1openalex-snapshot

Lignans and lignan glycosides fromHaplophyllum cappadocicum

inferredcites →https://doi.org/10.1016/s0031-9422(00)89595-3openalex-snapshot

4-O-Demethylyatein from the branch wood ofThuja occidentalis

inferredcites →https://doi.org/10.1016/s0031-9422(00)89605-3openalex-snapshot

An alkaloid and two lignans fromCuscuta chinensis

inferredcites →https://doi.org/10.1016/s0031-9422(00)89611-9openalex-snapshot

A 3-oxygenated flavonolignoid fromDistemonanthus benthamianus

inferredcites →https://doi.org/10.1016/s0031-9422(00)89656-9openalex-snapshot

Protolimonoid and lignans from Zanthoxylum petiolare

inferredcites →https://doi.org/10.1016/s0031-9422(00)89818-0openalex-snapshot

Lignans and an aromatic acid from Cinnamomum philippinense

inferredcites →https://doi.org/10.1016/s0031-9422(00)89819-2openalex-snapshot

Neolignans and an isoprenylated phenol from Piper clarkii

inferredcites →https://doi.org/10.1016/s0031-9422(00)90373-xopenalex-snapshot

Lignans and other constituents of Zanthoxylum heitzii

inferredcites →https://doi.org/10.1016/s0031-9422(00)90485-0openalex-snapshot

A lignan from needles of himalayan taxus baccata

inferredcites →https://doi.org/10.1016/s0031-9422(00)90571-5openalex-snapshot

Insect growth inhibitors from Machilus japonica

inferredcites →https://doi.org/10.1016/s0031-9422(00)90572-7openalex-snapshot

An insect growth inhibitory lignan from flower buds of Magnolia fargesii

inferredcites →https://doi.org/10.1016/s0031-9422(00)90743-xopenalex-snapshot

Lignans in flower buds of Magnolia saulangiana

inferredcites →https://doi.org/10.1016/s0031-9422(00)90836-7openalex-snapshot

Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger

inferredcites →https://doi.org/10.1016/s0031-9422(00)90857-4openalex-snapshot

Bisepoxylignan glycosides from Stauntonia hexaphylla

inferredcites →https://doi.org/10.1016/s0031-9422(00)94531-xopenalex-snapshot

Eusiderins and other neolignans from an Aniba species

inferredcites →https://doi.org/10.1016/s0031-9422(00)94786-1openalex-snapshot

Lignans and a stilbene from Festuca argentina

inferredcites →https://doi.org/10.1016/s0031-9422(00)94820-9openalex-snapshot

Microbial oxidation of (+)-epimagnolin a by Aspergillus niger

inferredcites →https://doi.org/10.1016/s0031-9422(00)94851-9openalex-snapshot

Norlignan glucosides from Curculigo recurvata

inferredcites →https://doi.org/10.1016/s0031-9422(00)95007-6openalex-snapshot

Phenylethanoid and lignan-iridoid complex glycosides from roots of Buddleja davidii

inferredcites →https://doi.org/10.1016/s0031-9422(00)95012-xopenalex-snapshot

Lignans and neolignans from Piper schmidtii

inferredcites →https://doi.org/10.1016/s0031-9422(00)95108-2openalex-snapshot

Schisantherins LO and acetylschisantherin L from Kadsura coccinea

inferredcites →https://doi.org/10.1016/s0031-9422(00)95121-5openalex-snapshot

Ocobullenone: A bicyclo[3.2.1]octanoid neolignan from Ocotea bullata

inferredcites →https://doi.org/10.1016/s0031-9422(00)95149-5openalex-snapshot

Formation of (−)-arctigenin in Forsythia intermedia

inferredcites →https://doi.org/10.1016/s0031-9422(00)97039-0openalex-snapshot

Nor-neolignan and phenyl propanoid from Zanthoxylum ailanthoides

inferredcites →https://doi.org/10.1016/s0031-9422(00)97101-2openalex-snapshot

Lignans and other compounds from the mixe indian medicinal plant Hyptis verticillata

inferredcites →https://doi.org/10.1016/s0031-9422(00)97102-4openalex-snapshot

Neolignans from bark and leaves of Ocotea porosa

inferredcites →https://doi.org/10.1016/s0031-9422(00)97110-3openalex-snapshot

Absolute configuration of the lignan oleiferins from Virola oleifera

inferredcites →https://doi.org/10.1016/s0031-9422(00)97544-7openalex-snapshot

On the stereoselective synthesis of (+)-pinoresinol in Forsythia suspensa from its achiral precursor, coniferyl alcohol

inferredcites →https://doi.org/10.1016/s0031-9422(00)97570-8openalex-snapshot

Biphenylneolignans from wood of Eurycoma longifolia

inferredcites →https://doi.org/10.1016/s0031-9422(00)97749-5openalex-snapshot

Effect of lignans and other secondary metabolites of the asteraceae on the mono-oxygenase activity of the european corn borer

inferredcites →https://doi.org/10.1016/s0031-9422(00)97835-xopenalex-snapshot

Lignan glycosides from Parsonsia laevigata

inferredcites →https://doi.org/10.1016/s0031-9422(00)97848-8openalex-snapshot

Ganschisandrine, a lignan from Schisandra sphenanthera

inferredcites →https://doi.org/10.1016/s0031-9422(00)97894-4openalex-snapshot

Neolignans and nor-neolignans from Krameria lanceolata

inferredcites →https://doi.org/10.1016/s0031-9422(00)97948-2openalex-snapshot

Neolignans from Licaria aurea

inferredcites →https://doi.org/10.1016/s0031-9422(00)98005-1openalex-snapshot

Aleuritin, a coumarinolignoid, and a coumarin from Aleurites fordii

inferredcites →https://doi.org/10.1016/s0031-9422(00)98010-5openalex-snapshot

Seven xanthonolignoids from Psorospermum febrifugum

inferredcites →https://doi.org/10.1016/s0031-9422(00)98039-7openalex-snapshot

Review article number 47

inferredcites →https://doi.org/10.1016/s0031-9422(00)98111-1openalex-snapshot

Lignans from Juniperus thurifera

inferredcites →https://doi.org/10.1016/s0031-9422(00)98242-6openalex-snapshot

Cannabisin A, an arylnaphthalene lignanamide from fruits of Cannabis sativa

inferredcites →https://doi.org/10.1016/s0031-9422(00)98258-xopenalex-snapshot

Synthesis of biologically active tetrahydro-furofuranlignan-(syringin, pinoresinol)- mono- and bis-glucosides

inferredcites →https://doi.org/10.1016/s0040-4020(01)80536-6openalex-snapshot

Efficient asymmetric syntheses of naturally occurring lignan lactones using catalytic asymmetric hydrogenation as a key reaction

inferredcites →https://doi.org/10.1016/s0040-4020(01)80826-7openalex-snapshot

Ruthenium dioxide in fluoro acid medium V. Application to the non phenolic oxidative coupling of diarylbutanes. Conformational studies of and deoxyschizandrins.

inferredcites →https://doi.org/10.1016/s0040-4020(01)80904-2openalex-snapshot

Ruthenium dioxide in fluoro acid medium: I. A new agent in the biaryl oxidative coupling. Application to the synthesis of non phenolic bisbenzocyclooctadiene lignan lactones.

inferredcites →https://doi.org/10.1016/s0040-4020(01)81005-xopenalex-snapshot

Isolation, structure and synthesis of new diarylbutane lignans from Phyllanthus niruri : Synthesis of 5′ -desmethoxy niranthin and an antitumour extractive

inferredcites →https://doi.org/10.1016/s0040-4020(01)81024-3openalex-snapshot

Reaction of gmelinol with triethylsilane and BF3-etherate - rearrangement of the 2.6-diaryl-3,7-dioxabicyclo[3.3.0]octane skeleton

inferredcites →https://doi.org/10.1016/s0040-4020(01)81924-4openalex-snapshot

Stereoselective total synthesis of (±)-Paulownin and (±)-Isogmelinol through radical annulation route

inferredcites →https://doi.org/10.1016/s0040-4020(01)82009-3openalex-snapshot

An enantioselective total synthesis of epiisopodophyllotoxin

inferredcites →https://doi.org/10.1016/s0040-4020(01)85081-xopenalex-snapshot

Lignans and neolignans from stems and fruits of Piper wightii

inferredcites →https://doi.org/10.1016/s0040-4020(01)85735-5openalex-snapshot

Synthesis of podophyllotoxin derivatives by means of tributyltin hydride- or palladium-mediated cyclization of α-benzylidene-β-(o-bromobenzyl)-γ-lactones

inferredcites →https://doi.org/10.1016/s0040-4020(01)86384-5openalex-snapshot

Oxidative transformations of lignans - reactions of dihydrocubebin and a derivative with DDQ

inferredcites →https://doi.org/10.1016/s0040-4020(01)86473-5openalex-snapshot

Enantioselective total synthesis of (−)-epipodophyllotoxin and (−)-podophyllotoxin

inferredcites →https://doi.org/10.1016/s0040-4020(01)87016-2openalex-snapshot

Lignanes. 17. Recherches sur la synthèse totale d'un norcyclonéolignane, la métaséquirine-B

inferredcites →https://doi.org/10.1016/s0040-4020(01)87053-8openalex-snapshot

Natural products syntheses using anodic oxidation of phenols as a key step

inferredcites →https://doi.org/10.1016/s0040-4020(01)87544-xopenalex-snapshot

Synthesis of new aryltetralin lignans

inferredcites →https://doi.org/10.1016/s0040-4020(01)87810-8openalex-snapshot

Asymmetric synthesis of lignans

inferredcites →https://doi.org/10.1016/s0040-4020(01)87949-7openalex-snapshot

Synthesis of non-phenolic bisbenzocyclooctadiene lignan lactones and aporphinic alkaloids, by oxidative coupling with new agents in fluoro acid medium. IV.

inferredcites →https://doi.org/10.1016/s0040-4020(01)88028-5openalex-snapshot

Synthesis and chemistry of thia-analogs of the anti-mitotic podophyllium lignans

inferredcites →https://doi.org/10.1016/s0040-4020(01)88129-1openalex-snapshot

Lignanes. 15. Première Synthèse Totale de la (−)-α-Conidendrine Naturelle

inferredcites →https://doi.org/10.1016/s0040-4020(01)88186-2openalex-snapshot

Ruthenium dioxide in fluoro acid medium: II. Application to the formation of steganes skeleton by oxidative phenolic coupling.

inferredcites →https://doi.org/10.1016/s0040-4020(01)88261-2openalex-snapshot

Rearrangements of 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans reactions of paulownin and wodeshiol with triethylsilane and BF3-etherate

inferredcites →https://doi.org/10.1016/s0040-4020(01)89002-5openalex-snapshot

Neurotrophic sesquiterpene-neolignans from magnolia obovata: structure and neurotrophic activity

inferredcites →https://doi.org/10.1016/s0040-4020(01)89041-4openalex-snapshot

Lignanes. 16. Premières synthèses totales du (+)-wikstromol, de la (−)-trachélogénine, de la (−)-nortrachélogénine et des lignoïdes apparentés

inferredcites →https://doi.org/10.1016/s0040-4020(01)89135-3openalex-snapshot

Cyclooctadiene systems derived from austrobailignan-5: revised stereochemical assignments

inferredcites →https://doi.org/10.1016/s0040-4020(01)89274-7openalex-snapshot

The asymmetric synthesis of an isomer of podophyllotoxin

inferredcites →https://doi.org/10.1016/s0040-4020(01)89597-1openalex-snapshot

Lignans and neolignans from stems of Piper wightii

inferredcites →https://doi.org/10.1016/s0040-4020(01)89890-2openalex-snapshot

Design, synthesis, and structure-cytotoxity relationships of aza-steganes

inferredcites →https://doi.org/10.1016/s0040-4020(01)89913-0openalex-snapshot

Asymmetric synthesis XXVIII : Hydroxylated benzoquinolizidine analogues of podophyllotoxin via the (CN(R,S) method.

showing the first 200 of 435 · page through all 435

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112958zenodo-depositor-declared

Comprehensive study of Anthriscus sylvestris lignans

inferred← citeshttps://doi.org/10.1002/(sici)1098-1128(199909)19:5<348::aid-med3>3.0.co;2-uopenalex-snapshot

Metal-catalyzed asymmetric oxidations

inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(200003)2000:6<893::aid-ejoc893>3.0.co;2-uopenalex-snapshot

Formaldehyde SAMP-Hydrazone as a Neutral Formyl Anion Equivalent: Asymmetric Synthesis of Substituted β-Formyl δ-Lactones and Furofuran Lactones

inferred← citeshttps://doi.org/10.1002/9781118346747.ch7openalex-snapshot

Phytoestrogens

inferred← citeshttps://doi.org/10.1002/9781118682784.ch10openalex-snapshot

Structure and Chemical Properties of Lignans

inferred← citeshttps://doi.org/10.1002/9781118682784.ch11openalex-snapshot

Biological Properties of Lignans

inferred← citeshttps://doi.org/10.1002/9783527634606.ch18openalex-snapshot

Biomimetic Synthesis of Lignans

inferred← citeshttps://doi.org/10.1002/adsc.200600587openalex-snapshot

Synthesis of Biaryls via Palladium‐Catalyzed [2+2+2] Cocyclization of Arynes and Diynes: Application to the Synthesis of Arylnaphthalene Lignans

inferred← citeshttps://doi.org/10.1002/adsc.200900703openalex-snapshot

Facile and Efficient Synthesis of Hydrophenanthren‐1(2H)‐ones and Naphtho[2,1‐c]furan‐3(1H)‐ones by a Palladium‐Catalyzed Aryne Annulation Strategy

inferred← citeshttps://doi.org/10.1002/adsc.201300503openalex-snapshot

Copper‐Catalyzed Synthesis of α‐Naphthols from Enol Esters

inferred← citeshttps://doi.org/10.1002/adsc.201601207openalex-snapshot

Asymmetric Dearomatizative Diels–Alder Reaction for the Construction of Hydrodibenzo[b,d]furan Frameworks with Tetrasubstituted Stereogenic Centers

inferred← citeshttps://doi.org/10.1002/ange.200453809openalex-snapshot

Arylnaphthalene Lignans through Pd‐Catalyzed [2+2+2] Cocyclization of Arynes and Diynes: Total Synthesis of Taiwanins C and E

inferred← citeshttps://doi.org/10.1002/ange.200802611openalex-snapshot

Kurze stereoselektive Synthese von (−)‐Podophyllotoxin durch eine intermolekulare Eisen(III)‐katalysierte Friedel‐Crafts‐Alkylierung

inferred← citeshttps://doi.org/10.1002/anie.200453809openalex-snapshot

Arylnaphthalene Lignans through Pd‐Catalyzed [2+2+2] Cocyclization of Arynes and Diynes: Total Synthesis of Taiwanins C and E

inferred← citeshttps://doi.org/10.1002/anie.200802611openalex-snapshot

Concise Stereoselective Synthesis of (−)‐Podophyllotoxin by an Intermolecular Iron(III)‐Catalyzed Friedel–Crafts Alkylation

inferred← citeshttps://doi.org/10.1002/asia.200900307openalex-snapshot

Tuned CH Functionalization to Construct Aza‐Podophyllotoxin/Aza‐Conidendrin Derivatives by Means of Domino Cyclization

inferred← citeshttps://doi.org/10.1002/asia.201200817openalex-snapshot

Synthesis of 1‐Arylnaphthalenes by Gold‐Catalyzed One‐Pot Sequential Epoxide to Carbonyl Rearrangement and Cyclization with Arylalkynes

inferred← citeshttps://doi.org/10.1002/chem.200802341openalex-snapshot

Asymmetric Gold‐Catalyzed Hydroarylation/Cyclization Reactions

inferred← citeshttps://doi.org/10.1002/chem.200901212openalex-snapshot

Asymmetric [2,3]‐Wittig Rearrangement of Oxygenated Allyl Benzyl Ethers in the Presence of a Chiral di‐tBu‐bis(oxazoline) Ligand: A Novel Synthetic Approach to THF Lignans

inferred← citeshttps://doi.org/10.1002/chin.199533298openalex-snapshot

ChemInform Abstract: Lignans, Neolignans, and Related Compounds

inferred← citeshttps://doi.org/10.1002/chin.199927275openalex-snapshot

ChemInform Abstract: Lignans, Neolignans, and Related Compounds

inferred← citeshttps://doi.org/10.1002/chir.10242openalex-snapshot

First asymmetric synthesis of (–)‐lintetralin via intramolecular Friedel‐Crafts‐type cyclization

inferred← citeshttps://doi.org/10.1002/ejoc.200400885openalex-snapshot

First Asymmetric Synthesis and Determination of the Absolute Configuration of a Lignan Isolated from Virola sebifera

inferred← citeshttps://doi.org/10.1002/ejoc.200600560openalex-snapshot

Cascade Reactions of Aromatic Aldehydes with Electron‐Deficient Acetylenes: Regioselective Construction of Diverse Aromatic Ring Systems

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Efficient Synthesis of Benzofurans Utilizing [3,3]‐Sigmatropic Rearrangement Triggered by N ‐Trifluoroacetylation of Oxime Ethers: Short Synthesis of Natural 2‐Arylbenzofurans

inferred← citeshttps://doi.org/10.1002/ejoc.200701027openalex-snapshot

Synthesis of Novel Angular Heterocyclic Lignans by an InCl3‐Catalyzed Friedel–Crafts‐Type Cyclization

inferred← citeshttps://doi.org/10.1002/ejoc.200800880openalex-snapshot

Heterolignans: Stereoselective Synthesis of an 11‐Amino Analog of Azaelliptitoxin

inferred← citeshttps://doi.org/10.1002/ejoc.200900099openalex-snapshot

Access to Enantiopure 2,5‐Diaryltetrahydrofurans – Application to the Synthesis of (–)‐Virgatusin and (+)‐Urinaligran

inferred← citeshttps://doi.org/10.1002/ejoc.200900643openalex-snapshot

Efficient Rhodium‐Catalyzed Conjugate Addition of Arylboronic Acids to Unsaturated Furano Esters for the Highly Stereoselective Synthesis of Four Natural Trisubstituted Furanolignans

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Highly Selective Electrophile‐Induced Cascade Reactions between o‐Alkynylbenzaldehydes and Styrene Oxides Leading to the Formation of 1‐Naphthyl Ketones

inferred← citeshttps://doi.org/10.1002/ejoc.201000497openalex-snapshot

ZnI2‐Catalyzed Benzannulation of o‐Alkynylbenzaldehydes with Alkenes Leading to 1‐Acyl‐2‐Substituted Naphthalenes

inferred← citeshttps://doi.org/10.1002/ejoc.201001112openalex-snapshot

An Efficient Synthesis of Polysubstituted Naphthalene Derivatives by Gold‐Catalyzed Cyclization of 1‐Arylalka‐2,3‐dienyl Acetates

inferred← citeshttps://doi.org/10.1002/ejoc.201601611openalex-snapshot

An Optimized and General Synthetic Strategy To Prepare Arylnaphthalene Lactone Natural Products from Cyanophthalides

inferred← citeshttps://doi.org/10.1002/hlca.200890252openalex-snapshot

Three New Arylnaphthalide Lignans from the Aerial Parts of Bupleurum marginatum Wall . ex DC.

inferred← citeshttps://doi.org/10.1002/hlca.200890256openalex-snapshot

Lignans from the Bark of Magnolia kobus

inferred← citeshttps://doi.org/10.1002/jccs.201190063openalex-snapshot

Hypervalent Iodine(III) Reagent Mediated Synthesis of 2‐Methylbenzofuran Derivatives by Pummerer‐type Reaction in Ionic Liquid

inferred← citeshttps://doi.org/10.1002/jccs.201800320openalex-snapshot

Synthesis of tetrahydrobenzo[b]furans via a gold(I)‐catalyzed rearrangement/cycloisomerization sequence of cyclic 1‐aryl‐2‐propargyl‐cyclohex‐2enols

inferred← citeshttps://doi.org/10.1002/jhet.5570360134openalex-snapshot

Synthesis and absolute configuration of (‐)‐meridinol and (‐)‐3‐epimeridinol

inferred← citeshttps://doi.org/10.1002/jlac.199619960904openalex-snapshot

Diastereo‐ and Enantioselective Synthesis of Lignan Building Blocks by Tandem Michael Addition/Electrophilic Substitution of Lithiated α‐Amino Nitriles to Furan‐2(5H)‐one

inferred← citeshttps://doi.org/10.1002/jlac.199719970616openalex-snapshot

First Total Synthesis of (+)‐Membrine

inferred← citeshttps://doi.org/10.1002/mrc.1260321210openalex-snapshot

Influence of skeletal alteration of lignoids on carbon‐13 NMR chemical shifts

inferred← citeshttps://doi.org/10.1002/poc.1089openalex-snapshot

Asymmetric biomimetic oxidations of phenols using oxazolidines as chiral auxiliaries: the enantioselective synthesis of (+)‐ and (−)‐dehydrodiconiferyl alcohol

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Pharmacological properties, therapeutic potential, and legal status of Cannabis sativa L.: An overview

inferred← citeshttps://doi.org/10.1002/rcm.3243openalex-snapshot

Electrospray ionization ion‐trap time‐of‐flight tandem mass spectrometry of two furofurans: sesamin and gmelinol

inferred← citeshttps://doi.org/10.1006/abio.2000.4811openalex-snapshot

Extraction and Quantification of Lignan Phytoestrogens in Food and Human Samples

inferred← citeshttps://doi.org/10.1007/978-3-642-22144-6_25openalex-snapshot

Alkaloids Derived from Anthranilic Acid: Quinoline, Acridone, and Quinazoline

inferred← citeshttps://doi.org/10.1007/978-3-642-22144-6_57openalex-snapshot

Phenolic Compounds: Introduction

inferred← citeshttps://doi.org/10.1007/978-3-642-33173-2_3openalex-snapshot

The Synthesis of Naphthalenes and Biaryls

inferred← citeshttps://doi.org/10.1007/978-981-16-3529-8_13openalex-snapshot

Production of Antidiabetic Lignans in Flax Cell Cultures

inferred← citeshttps://doi.org/10.1007/bf02980039openalex-snapshot

Synthesis of 2-(4-hydroxyphenyl)benzofurans and their application to β-amyloid aggregation inhibitor

inferred← citeshttps://doi.org/10.1007/pl00001826openalex-snapshot

Lignoid chemical defenses in the freshwater macrophyte Saururus cernuus

inferred← citeshttps://doi.org/10.1007/s00044-012-0052-8openalex-snapshot

Synthesis and biological evaluation of gallic acid analogs

inferred← citeshttps://doi.org/10.1007/s00425-019-03137-yopenalex-snapshot

Pinoresinol–lariciresinol reductases, key to the lignan synthesis in plants

inferred← citeshttps://doi.org/10.1007/s004250000326openalex-snapshot

Phenylcoumaran benzylic ether reductase, a prominent poplar xylem protein, is strongly associated with phenylpropanoid biosynthesis in lignifying cells

inferred← citeshttps://doi.org/10.1007/s10600-005-0067-1openalex-snapshot

Aryltetralin Lignans from Linum mucronatum Bertol. ssp. mucronatum

inferred← citeshttps://doi.org/10.1007/s10886-006-9038-7openalex-snapshot

Chemical Defenses Promote Persistence of the Aquatic Plant Micranthemum umbrosum

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Secondary metabolism in cannabis

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Chemical diversity and pharmacological significance of the secondary metabolites of nutmeg (Myristica fragrans Houtt.)

inferred← citeshttps://doi.org/10.1007/s11101-020-09668-7openalex-snapshot

Update on naturally occurring novel arylnaphthalenes from plants

inferred← citeshttps://doi.org/10.1007/s11172-011-0358-6openalex-snapshot

Stereospecific synthesis of endo-endo-3,7-dioxabicyclo[3.3.0]octane lignans using 1,6-bis(dipropylboryl)-2,4-hexadiene

inferred← citeshttps://doi.org/10.1007/s11172-022-3583-2openalex-snapshot

Total synthesis of diaeudesmin and epieudesmin enantiomers from diallyl

inferred← citeshttps://doi.org/10.1007/s11224-016-0758-1openalex-snapshot

The role of cesium fluoride in aryl propargyl ether Claisen rearrangement and its mechanistic elucidation: a theoretical study

inferred← citeshttps://doi.org/10.1007/s11426-013-4843-7openalex-snapshot

Synthesis of naphthalene derivatives through inexpensive BF3·Et2O-catalyzed annulation reaction of arylacetaldehydes with arylalkynes

inferred← citeshttps://doi.org/10.1007/s11745-005-1449-2openalex-snapshot

Astonishing diversity of natural surfactants: 5. Biologically active glycosides of aromatic metabolites

inferred← citeshttps://doi.org/10.1007/s12039-010-0050-7openalex-snapshot

Total synthesis of (±)-divanillyltetrahydrofuran ferulate

inferred← citeshttps://doi.org/10.1007/s12039-014-0599-7openalex-snapshot

First total synthesis of Boehmenan

inferred← citeshttps://doi.org/10.1007/s12094-007-0138-9openalex-snapshot

Natural products as leads to anticancer drugs

inferred← citeshttps://doi.org/10.1007/s12272-017-0908-zopenalex-snapshot

Effects of asarinin on dopamine biosynthesis and 6-hydroxydopamine-induced cytotoxicity in PC12 cells

inferred← citeshttps://doi.org/10.1007/s13659-015-0073-3openalex-snapshot

Total Synthesis of Lignan Lactone (–)-Hinokinin

inferred← citeshttps://doi.org/10.1007/s13738-017-1149-2openalex-snapshot

A green, simple, catalyst-free, and efficient method for electro-organic synthesis of new benzofuran derivatives

inferred← citeshttps://doi.org/10.1016/0040-4020(96)00761-2openalex-snapshot

Asymmetric synthesis of a lignan lactone from a meso anhydride

inferred← citeshttps://doi.org/10.1016/0040-4039(95)01866-gopenalex-snapshot

Sequential and regioselective Friedel-Crafts reactions of gem-dihalocyclopropanecarbonyl chlorides with benzenes for the synthesis of 4-aryl-l-naphthol derivatives

inferred← citeshttps://doi.org/10.1016/0040-4039(96)00355-3openalex-snapshot

A new approach to the synthesis of podophyllotoxin based on epimerization reactions

inferred← citeshttps://doi.org/10.1016/0040-4039(96)01619-xopenalex-snapshot

Synthesis of (±)-licarin B and eupomatenoids-1 and -12: A general approach to 2-aryl-7-alkoxy-benzofuranoid neolignans

inferred← citeshttps://doi.org/10.1016/b978-0-08-091283-7.00027-8openalex-snapshot

Lignans: Biosynthesis and Function

inferred← citeshttps://doi.org/10.1016/b978-0-12-405927-6.00012-6openalex-snapshot

Lignans and Stilbenes from African Medicinal Plants

inferred← citeshttps://doi.org/10.1016/b978-0-444-59603-1.00006-0openalex-snapshot

Progress in the Syntheses of Dibenzocyclooctadiene Lignans

inferred← citeshttps://doi.org/10.1016/b978-0-7020-2933-2.00021-6openalex-snapshot

Phenols and phenolic glycosides

inferred← citeshttps://doi.org/10.1016/b978-1-60805-999-7.50001-xopenalex-snapshot

Application of NMR Spectroscopy in Plant Polyphenols Associated with Human Health

inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.08.033openalex-snapshot

Stereoisomeric guaiacylglycerol-β-coniferyl aldehyde ether induces distinctive apoptosis by downregulation of MEK/ERK pathway in hepatocellular carcinoma cells

inferred← citeshttps://doi.org/10.1016/j.bmc.2010.12.044openalex-snapshot

Synthesis of egonol derivatives and their antimicrobial activities

inferred← citeshttps://doi.org/10.1016/j.bmc.2015.09.039openalex-snapshot

Ring substitution influences oxidative cyclisation and reactive metabolite formation of nordihydroguaiaretic acid analogues

inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.10.079openalex-snapshot

Trypanocidal activity of (−)-cubebin derivatives against free amastigote forms of Trypanosoma cruzi

inferred← citeshttps://doi.org/10.1016/j.bse.2008.05.007openalex-snapshot

Chemical constituents from Pleurothyrium cinereum (van der Werff) (Lauraceae) from Colombia

inferred← citeshttps://doi.org/10.1016/j.cclet.2016.03.040openalex-snapshot

An efficient etherification of Ginkgol biloba extracts with fewer side effects in a micro-flow system

inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.12.028openalex-snapshot

Hydroxylated biphenyls as tyrosinase inhibitor: A spectrophotometric and electrochemical study

inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114659openalex-snapshot

SILAC-based chemoproteomics reveals a neoligan analogue as an anti-inflammatory agent targeting IRGM to ameliorate cytokine storm

inferred← citeshttps://doi.org/10.1016/j.ejphar.2017.01.044openalex-snapshot

Diethyl-4,4ʹ-dihydroxy-8,3ʹ-neolign-7,7ʹ-dien-9,9ʹ-dionate exhibits antihypertensive activity in rats through increase in intracellular cGMP level and blockade of calcium channels

inferred← citeshttps://doi.org/10.1016/j.fitote.2005.07.007openalex-snapshot

Biological activity of some Patagonian plants

inferred← citeshttps://doi.org/10.1016/j.fitote.2016.07.004openalex-snapshot

Five furofuranone lignan glucosides from Terminalia citrina inhibit in vitro E2-enhanced breast cancer cell proliferation

inferred← citeshttps://doi.org/10.1016/j.jep.2005.07.021openalex-snapshot

Anti-inflammatory activities of constituents isolated from Phyllanthus polyphyllus

inferred← citeshttps://doi.org/10.1016/j.jep.2019.112087openalex-snapshot

Tocolytic activity assessment of the methanol leaf extract of Justicia flava Vahl (Acanthaceae) on mouse myometrial contractility and preliminary mass spectrometric determination of secondary metabolites

inferred← citeshttps://doi.org/10.1016/j.jff.2014.02.017openalex-snapshot

Identification of sesquilignans in litchi (Litchi chinensis Sonn.) leaf and their anticancer activities

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.09.062openalex-snapshot

ZnCl2-catalyzed [4 + 2] benzannulation of 2-ethynylbenzaldehydes with alkynes: Selective synthesis of naphthalene derivatives

inferred← citeshttps://doi.org/10.1016/j.neuint.2015.01.003openalex-snapshot

Effects of (-)-sesamin on 6-hydroxydopamine-induced neurotoxicity in PC12 cells and dopaminergic neuronal cells of Parkinson's disease rat models

inferred← citeshttps://doi.org/10.1016/j.pharep.2014.07.005openalex-snapshot

Apoptotic mechanisms of the biotechnologically produced arylnaphtalene lignan justicidin B in the acute myeloid leukemia-derived cell line HL-60

inferred← citeshttps://doi.org/10.1016/j.phymed.2013.03.026openalex-snapshot

Apoptosis inducing activity of benzophenanthridine-type alkaloids and 2-arylbenzofuran neolignans in HCT116 colon carcinoma cells

inferred← citeshttps://doi.org/10.1016/j.phytochem.2009.05.016openalex-snapshot

Glycosides of arylnaphthalene lignans from Acanthus mollis having axial chirality

inferred← citeshttps://doi.org/10.1016/j.phytochem.2009.12.008openalex-snapshot

Metabolic responses of Thellungiella halophila/salsuginea to biotic and abiotic stresses: Metabolite profiles and quantitative analyses

inferred← citeshttps://doi.org/10.1016/j.phytol.2013.03.009openalex-snapshot

Two new dihydrobenzofuran-type neolignans from Breynia fruticosa

inferred← citeshttps://doi.org/10.1016/j.plaphy.2013.05.009openalex-snapshot

Plant phenolics: Recent advances on their biosynthesis, genetics, and ecophysiology

inferred← citeshttps://doi.org/10.1016/j.steroids.2005.10.005openalex-snapshot

Synthesis of multiply 13C-labeled furofuran lignans using 13C-labeled cinnamyl alcohols as building blocks

inferred← citeshttps://doi.org/10.1016/j.tet.2005.03.069openalex-snapshot

Syntheses of (±)-thuriferic acid ethyl ester, its analogues and (±)-picropodophyllone

inferred← citeshttps://doi.org/10.1016/j.tet.2005.12.013openalex-snapshot

Cobalt-catalyzed cross-coupling reactions of alkyl halides with aryl Grignard reagents and their application to sequential radical cyclization/cross-coupling reactions

inferred← citeshttps://doi.org/10.1016/j.tet.2006.03.111openalex-snapshot

An efficient method for the synthesis of lignans

inferred← citeshttps://doi.org/10.1016/j.tet.2006.09.026openalex-snapshot

1-Aryltetralin privileged structure-based libraries: parallel synthesis of N-aryl and N-biaryl γ-lactam lignans

inferred← citeshttps://doi.org/10.1016/j.tet.2007.01.054openalex-snapshot

Claisen rearrangement/Baylis–Hillman reaction/ring-closing metathesis as bases for the construction of substituted cyanonaphthalenes

inferred← citeshttps://doi.org/10.1016/j.tet.2007.03.063openalex-snapshot

Structure and neurotrophic activity of novel sesqui-neolignans from the pericarps of Illicium fargesii

inferred← citeshttps://doi.org/10.1016/j.tet.2008.05.114openalex-snapshot

Intriguing formal [2+3] cycloaddition promoted by a hypervalent iodine reagent

inferred← citeshttps://doi.org/10.1016/j.tet.2013.04.118openalex-snapshot

5-Hydroxypent-2-enenitriles as precursors toward dihydropyranones, dienenitriles and functionalized naphthalenes

inferred← citeshttps://doi.org/10.1016/j.tet.2014.01.005openalex-snapshot

Synthesis of substituted naphthalenes from α-substituted ketones and 1,2-bis(halomethyl)benzenes including a rearrangement aromatization of benzo[c]oxepine

inferred← citeshttps://doi.org/10.1016/j.tet.2016.10.058openalex-snapshot

Electochemical asymmetric dimerization of cinnamic acid derivatives and application to the enantioselective syntheses of furofuran lignans

inferred← citeshttps://doi.org/10.1016/j.tet.2017.07.058openalex-snapshot

Access to polysubstituted naphthalenes and anthracenes via a retro-Diels–Alder reaction

inferred← citeshttps://doi.org/10.1016/j.tet.2018.09.010openalex-snapshot

Ruthenium-catalyzed annulation of aromatic ketones with internal alkynes: A reliable route to substituted naphthalene derivatives

inferred← citeshttps://doi.org/10.1016/j.tetasy.2003.08.002openalex-snapshot

Access to optically active 2,2′-dihydroxy-6,6′-dimethoxy-1,1′-biphenyl by a simple biocatalytic procedure

inferred← citeshttps://doi.org/10.1016/j.tetasy.2005.11.007openalex-snapshot

An efficient asymmetric synthesis of furofuran lignans: (+)-sesamin and (−)-sesamin

inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.06.127openalex-snapshot

Stereoselective total synthesis of furofuran lignans through dianion aldol condensation

inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.11.202openalex-snapshot

Pseudo-domino palladium-catalyzed allylic alkylation/Mizoroki–Heck coupling reaction: a key sequence toward (±)-podophyllotoxin

inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.03.105openalex-snapshot

A stereocontrolled approach for the synthesis of 2,5-diaryl-3,4-disubstituted furano lignans through a highly diastereoselective aldol condensation of an ester enolate with an α-chiral center: total syntheses of (−)-talaumidin and (−)-virgatusin

inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.03.111openalex-snapshot

Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans via a two-step sequential Michael-Evans aldol cyclization strategy: total synthesis of (+)-magnolone

inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.10.136openalex-snapshot

An asymmetric route to total synthesis of the furano lignan (+)-veraguensin

inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.12.047openalex-snapshot

A facile domino protocol for the stereoselective synthesis of trans-2,3-dihydrobenzofurans and cis-5,6-dihydrofuro[2,3-d]pyrimidines

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.01.061openalex-snapshot

One-pot synthesis of 3-trifluoromethylbenzofurans via tandem iodocyclization and trifluoromethylation of 2-alkynylanisoles

inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.06.079openalex-snapshot

A novel tandem Pd-catalyzed intramolecular allylic decarboxylative coupling and “diradical conjugated 1,3-dien-5-yne cycloaromatization”: An unusual ortho -selectivity in the cycloaromatization and the mechanistic implications

inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156149openalex-snapshot

Indium chloride catalysed annulation of arylmethyl carbonyls & arylalkynes for the synthesis of naphthalene derivatives

inferred← citeshttps://doi.org/10.1016/j.toxicon.2004.05.007openalex-snapshot

Lignoids in insects: chemical probes for the study of ecdysis, excretion and Trypanosoma cruzi—triatomine interactions

inferred← citeshttps://doi.org/10.1016/j.toxicon.2004.05.008openalex-snapshot

Podophyllotoxin: distribution, sources, applications and new cytotoxic derivatives

inferred← citeshttps://doi.org/10.1016/s0022-2860(03)00221-7openalex-snapshot

Molecular structures of two bicyclo-(3.2.1)-octanoid neolignans from Piper kadsura

inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00076-5openalex-snapshot

Two antifeedant lignans from the freshwater macrophyte Saururus cernuus

inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00275-2openalex-snapshot

Cytotoxicity of extractives from Taiwania cryptomerioides heartwood

inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00477-5openalex-snapshot

Lipophyllic antioxidants from Iryanthera juruensis fruits

inferred← citeshttps://doi.org/10.1016/s0031-9422(03)00422-9openalex-snapshot

Two lignan dimers from bamboo stems (Phyllostachys edulis)

inferred← citeshttps://doi.org/10.1016/s0031-9422(96)00452-9openalex-snapshot

A sesquilignan from Illicium dunnianum

inferred← citeshttps://doi.org/10.1016/s0039-128x(01)00107-6openalex-snapshot

α,β-Dibenzyl-γ-butyrolactone lignan alcohols: total synthesis of (±)-7′-hydroxyenterolactone, (±)-7′-hydroxymatairesinol and (±)-8-hydroxyenterolactone

inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00469-0openalex-snapshot

Transformations of lignans. Part 4: Oxidative and reductive rearrangements of dibenzocyclooctadiene and spirodienone lignans

inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00616-6openalex-snapshot

A new benzannulation reaction and its application in the multiple parallel synthesis of arylnaphthalene lignans

inferred← citeshttps://doi.org/10.1016/s0040-4020(97)00310-4openalex-snapshot

Bioactive isoxazoline and oxime derivatives from 7-ketolignans

inferred← citeshttps://doi.org/10.1016/s0040-4020(97)10042-4openalex-snapshot

Preparation and cytotoxicity of podophyllotoxin derivatives lacking the lactone ring

inferred← citeshttps://doi.org/10.1016/s0040-4039(00)00145-3openalex-snapshot

A new route towards the synthesis of substituted naphthalenes via Friedel–Crafts acylation

inferred← citeshttps://doi.org/10.1016/s0040-4039(01)00431-2openalex-snapshot

Synthesis of naphthalenes using acid-catalyzed ring-opening and recyclization of 3-acetyl-5,5-diaryl-2-methyl-4,5-dihydrofurans. Isolation of intermediates

inferred← citeshttps://doi.org/10.1016/s0040-4039(02)02860-5openalex-snapshot

First synthesis of naturally occurring (±)-epi-conocarpan

inferred← citeshttps://doi.org/10.1016/s0040-4039(97)01713-9openalex-snapshot

Regiocontrolled benzannulation of diaryl(gem-dichlorocyclopropyl)methanols for the synthesis of “unsymmetrically” substituted α-arylnaphthalenes

inferred← citeshttps://doi.org/10.1016/s0040-4039(98)00116-6openalex-snapshot

Heterolignanolides. Synthesis of a new family of Thienolignanolides

inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01053-3openalex-snapshot

A new approach to 2-aryl-7-alkoxy-benzofurans: Synthesis of ailanthoidol, a natural neolignan

inferred← citeshttps://doi.org/10.1016/s0168-9452(01)00512-xopenalex-snapshot

Enantioselective conversion of p-hydroxypropenylbenzene to (+)-conocarpan in Piper regnellii

inferred← citeshttps://doi.org/10.1016/s0378-8741(98)00131-7openalex-snapshot

Antibacterial, antifungal and antiviral activity of propolis of different geographic origin

inferred← citeshttps://doi.org/10.1016/s0944-7113(97)80063-3openalex-snapshot

Cardiovascular activity of naturally occurring lignans

inferred← citeshttps://doi.org/10.1016/s0957-4166(98)00299-7openalex-snapshot

A chemoenzymatic synthesis of both enantiomers of a cis-lignan lactone

inferred← citeshttps://doi.org/10.1016/s0968-0896(00)00130-9openalex-snapshot

First synthesis and pharmacological evaluation of benzoindolizidine and benzoquinolizidine analogues of α- and β-peltatin

inferred← citeshttps://doi.org/10.1016/s1099-4831(07)64004-8openalex-snapshot

Chapter 4 Alkyl, Aryl, Alkylarylquinoline, and Related Alkaloids

inferred← citeshttps://doi.org/10.1016/s1572-5995(02)80008-4openalex-snapshot

New findings on the bioactivity of lignans

inferred← citeshttps://doi.org/10.1017/s0007114509992261openalex-snapshot

Dietary intake and urinary excretion of lignans in Finnish men

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00035openalex-snapshot

Neuroprotective Lignans from the Fruits of Schisandra bicolor var. tuberculata

inferred← citeshttps://doi.org/10.1021/acs.joc.3c01852openalex-snapshot

Copper(II)-Mediated, Site-Selective C(sp2)–H Sulfonamidation of 1-Naphthylamines

inferred← citeshttps://doi.org/10.1021/acs.joc.4c03186openalex-snapshot

Au(I) /Brønsted Acid Relay-Catalyzed Benzannulation Reaction of Alkynylbenzaldehydes and Styrenes for the Synthesis of Substituted Naphthalenes

inferred← citeshttps://doi.org/10.1021/acs.joc.5b00353openalex-snapshot

HNTf2-Catalyzed Regioselective Preparation of Polysubstituted Naphthalene Derivatives Through Alkyne–Aldehyde Coupling

inferred← citeshttps://doi.org/10.1021/acs.joc.5b00970openalex-snapshot

Stereoselective Synthesis of 1-Fluoro-exo,exo-2,6-diaryl-3,7-dioxabicyclo[3.3.0]octanes: Synthesis of (±)-1-Fluoromembrine

inferred← citeshttps://doi.org/10.1021/acs.joc.6c00021openalex-snapshot

Synthesis of 2-Naphthols via a Trifluoroacetic Acid-Mediated Epoxy Alcohol Rearrangement

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01477openalex-snapshot

Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03186openalex-snapshot

Bromide-Mediated C–H Bond Functionalization: Intermolecular Annulation of Phenylethanone Derivatives with Alkynes for the Synthesis of 1-Naphthols

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01707openalex-snapshot

Synthesis of 1,2,3-Triazolo-Fused Allocolchicine Analogs via Intramolecular Oxidative Biaryl Coupling

inferred← citeshttps://doi.org/10.1021/acscatal.1c00629openalex-snapshot

In(III)-Catalyzed Direct Regioselective Syntheses of 1-Naphthaldehyde Derivatives via a Hidden Aldehyde 1,3-Translocation and Disjointed CO2 Extrusion

inferred← citeshttps://doi.org/10.1021/acscatal.6b03671openalex-snapshot

Copper-Catalyzed Remote C–H Functionalizations of Naphthylamides through a Coordinating Activation Strategy and Single-Electron-Transfer (SET) Mechanism

inferred← citeshttps://doi.org/10.1021/cr050531bopenalex-snapshot

Progress on the Chemistry of Dibenzocyclooctadiene Lignans

inferred← citeshttps://doi.org/10.1021/jo010522copenalex-snapshot

Induction of a Preferred Sense of Twist in Flexible Diphenyls by Carbohydrate Scaffolds. Synthesis of Two “Naked” Ellagitannin Analogous

inferred← citeshttps://doi.org/10.1021/jo011077oopenalex-snapshot

Total Synthesis of Two Naturally Occurring Bicyclo[3.2.1]octanoid Neolignans

inferred← citeshttps://doi.org/10.1021/jo0157627openalex-snapshot

Regiocontrolled Synthesis of Enantiopure 3,3‘-Thiosubstituted Biphenyls

inferred← citeshttps://doi.org/10.1021/jo0161025openalex-snapshot

Acid-Catalyzed Cyclization of 2,3-Dibenzylidenesuccinates: Synthesis of Lignans (±)-Cagayanin and (±)-Galbulin

inferred← citeshttps://doi.org/10.1021/jo016220sopenalex-snapshot

Total Synthesis of (S)-(+)-Imperanene. Effective Use of Regio- and Enantioselective Intramolecular Carbon−Hydrogen Insertion Reactions Catalyzed by Chiral Dirhodium(II) Carboxamidates

inferred← citeshttps://doi.org/10.1021/jo034330oopenalex-snapshot

A New Titanium Tetrachloride Mediated Annulation of α-Aryl-Substituted Carbonyl Compounds with Alkynes: A Simple and Highly Efficient Method for the Regioselective Synthesis of Polysubstituted Naphthalene Derivatives

inferred← citeshttps://doi.org/10.1021/jo034449xopenalex-snapshot

Synthesis of Substituted Naphthalenes and Carbazoles by the Palladium-Catalyzed Annulation of Internal Alkynes

inferred← citeshttps://doi.org/10.1021/jo047751uopenalex-snapshot

Regiocontrolled Benzannulation of Diaryl(gem-dichlorocyclopropyl)methanols for the Synthesis of Unsymmetrically Substituted α-Arylnaphthalenes: Application to Total Synthesis of Natural Lignan Lactones

inferred← citeshttps://doi.org/10.1021/jo0500941openalex-snapshot

A Rapid Synthesis of 2-Aryl-5-substituted-2,3-dihydrobenzofurans

inferred← citeshttps://doi.org/10.1021/jo051299copenalex-snapshot

Synthesis of 2,3-Disubstituted Benzo[b]furans by the Palladium-Catalyzed Coupling ofo-Iodoanisoles and Terminal Alkynes, Followed by Electrophilic Cyclization

inferred← citeshttps://doi.org/10.1021/jo051948kopenalex-snapshot

Synthesis of Naphthalenes and 2-Naphthols by the Electrophilic Cyclization of Alkynes

inferred← citeshttps://doi.org/10.1021/jo070241qopenalex-snapshot

A Novel Multicomponent Reaction of Arynes, β-Keto Sulfones, and Michael-Type Acceptors: A Direct Synthesis of Polysubstituted Naphthols and Naphthalenes

inferred← citeshttps://doi.org/10.1021/jo200352jopenalex-snapshot

Synthesis of 2-Phenylnaphthalenes through Gold-Catalyzed Dimerization via a Highly Selective Carbon Nucleophile Pathway

inferred← citeshttps://doi.org/10.1021/jo400244hopenalex-snapshot

CuCN-Mediated Cascade Cyclization of 4-(2-Bromophenyl)-2-butenoates: A High-Yield Synthesis of Substituted Naphthalene Amino Esters

inferred← citeshttps://doi.org/10.1021/jo4017748openalex-snapshot

How the Bicyclo[4.1.0] Substrate Isomerizes into 4,5-Dihydrobenzo[b]furan: The Contribution from W(CO)5 and NEt3

inferred← citeshttps://doi.org/10.1021/jo800901ropenalex-snapshot

Stereoselective Synthesis of 3-Alkyl-2-aryltetrahydrofuran-4-ols: Total Synthesis of (±)-Paulownin

inferred← citeshttps://doi.org/10.1021/jo9016309openalex-snapshot

PdCl2-Promoted Electrophilic Annulation of 2-Alkynylphenol Derivatives with Disulfides or Diselenides in the Presence of Iodine

inferred← citeshttps://doi.org/10.1021/jo961607uopenalex-snapshot

Intramolecular Regioselective Insertion into Unactivated Prochiral Carbon−Hydrogen Bonds with Diazoacetates of Primary Alcohols Catalyzed by Chiral Dirhodium(II) Carboxamidates. Highly Enantioselective Total Synthesis of Natural Lignan Lactones

inferred← citeshttps://doi.org/10.1021/jo961744ropenalex-snapshot

Efficient Synthesis of 1-Amino-2-naphthalenecarboxylic Acid Derivatives via a Sequential Michael Addition/Enolate−Nitrile Coupling Route and Its Application to Facile Preparation of 9-Amino Analogues of Arylnaphthofuranone Lignans

inferred← citeshttps://doi.org/10.1021/jo971027copenalex-snapshot

Asymmetric Synthesis of Sesaminone: Confirmation of Its Structure and Determination of Its Absolute Configuration

inferred← citeshttps://doi.org/10.1021/np9000569openalex-snapshot

Macrophyllin-Type Bicyclo[3.2.1]octanoid Neolignans from the Leaves of Pleurothyrium cinereum

inferred← citeshttps://doi.org/10.1021/ol026128yopenalex-snapshot

Synthesis of Substituted Naphthalenes by the Palladium-Catalyzed Annulation of Internal Alkynes

inferred← citeshttps://doi.org/10.1021/ol034806qopenalex-snapshot

Ruthenium Porphyrin Catalyzed Intramolecular Carbenoid C−H Insertion. Stereoselective Synthesis of Cis-Disubstituted Oxygen and Nitrogen Heterocycles

inferred← citeshttps://doi.org/10.1021/ol060908fopenalex-snapshot

Novel and Selective Palladium-Catalyzed Annulations of 2-Alkynylphenols To Form 2-Substituted 3-Halobenzo[b]furans

inferred← citeshttps://doi.org/10.1021/ol302437vopenalex-snapshot

Synthesis of Naphthalenes via Platinum-Catalyzed Hydroarylation of Aryl Enynes

inferred← citeshttps://doi.org/10.1021/ol4000394openalex-snapshot

Iron-catalyzed Benzannulation Reactions of 2-Alkylbenzaldehydes and Alkynes Leading to Naphthalene Derivatives

inferred← citeshttps://doi.org/10.1021/ol400792yopenalex-snapshot

Pd-Catalyzed π-Chelation Assisted ortho-C–H Activation and Annulation of Allylarenes with Internal Alkynes

inferred← citeshttps://doi.org/10.1021/ol401897uopenalex-snapshot

Synthesis of Dihydrobenzofurans with Quaternary Carbon Center under Mild and Neutral Conditions

inferred← citeshttps://doi.org/10.1021/ol501683vopenalex-snapshot

Novel [4 + 2]-Benzannulation To Access Substituted Benzenes and Polycyclic Aromatic and Benzene-Fused Heteroaromatic Compounds

inferred← citeshttps://doi.org/10.1023/b:phyt.0000045488.84428.bdopenalex-snapshot

Different strategies for the chemical synthesis of lignans

inferred← citeshttps://doi.org/10.1023/b:phyt.0000045495.59732.58openalex-snapshot

Lignans in treatment of cancer and other diseases†

inferred← citeshttps://doi.org/10.1023/b:phyt.0000045501.97438.9copenalex-snapshot

Linum persicum: Lignans and placement in Linaceae†

inferred← citeshttps://doi.org/10.1038/ejcn.2012.45openalex-snapshot

Determinants of dietary lignan intake in a representative sample of young Spaniards: association with lower obesity prevalence among boys but not girls

inferred← citeshttps://doi.org/10.1038/s41467-018-02955-0openalex-snapshot

Selenide-catalyzed enantioselective synthesis of trifluoromethylthiolated tetrahydronaphthalenes by merging desymmetrization and trifluoromethylthiolation

inferred← citeshttps://doi.org/10.1039/a605288fopenalex-snapshot

A simple method for the synthesis of 4-aryl-9-oxynaphthofuranone lignans

inferred← citeshttps://doi.org/10.1039/a801620hopenalex-snapshot

Biomimetic Synthesis of Illicium Oligomeric Neolignans

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