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Two‐dimensional nuclear magnetic resonance of sesquiterpenes. 4—Application to complete assignment of 1H and 13C NMR spectra of some aromadendrane derivatives

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What this work says

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

inferredcites →https://doi.org/10.1002/mrc.1260240321openalex-snapshot

Carbon‐13 NMR spectra of five sesquiterpenes isolated from Ylang Ylang essential oil

inferredcites →https://doi.org/10.1002/mrc.1260241008openalex-snapshot

Two‐dimensional NMR of sesquiterpenic compounds. I—application to complete assignment of 1H and 13C spectra of α‐longipinene

inferredcites →https://doi.org/10.1016/0022-2364(78)90197-xopenalex-snapshot

Resolution enhancement in FT NMR through the use of a double exponential function

inferredcites →https://doi.org/10.1016/0022-2364(80)90255-3openalex-snapshot

Experimental techniques of two-dimensional correlated spectroscopy

inferredcites →https://doi.org/10.1016/0022-2364(81)90022-6openalex-snapshot

Correlation of proton chemical shifts by two-dimensional Fourier transform NMR

inferredcites →https://doi.org/10.1016/0022-2364(81)90060-3openalex-snapshot

Assignment of carbon-13 NMR spectra via double-quantum coherence

inferredcites →https://doi.org/10.1016/0022-2364(82)90286-4openalex-snapshot

Distortionless enhancement of NMR signals by polarization transfer

inferredcites →https://doi.org/10.1016/0022-2364(83)90225-1openalex-snapshot

Broadband homonuclear decoupling in heteronuclear shift correlation NMR spectroscopy

inferredcites →https://doi.org/10.1016/0022-2364(84)90219-1openalex-snapshot

Suppression of homonuclear J couplings in 1H-13C chemical-shift correlation maps

inferredcites →https://doi.org/10.1016/0165-9936(83)80014-4openalex-snapshot

Two dimensional nuclear magnetic resonance in liquids

inferredcites →https://doi.org/10.1021/ja00398a044openalex-snapshot

An NMR technique for tracing out the carbon skeleton of an organic molecule

inferredcites →https://doi.org/10.1021/ja00997a001openalex-snapshot

Carbon-13 magnetic resonance. VII. Steric perturbation of the carbon-13 chemical shift

inferredcites →https://doi.org/10.1021/jf00088a048openalex-snapshot

Sesquiterpene composition of basil oil. Assignment of the proton and NMR carbon-13 spectra of .beta.-elemene with two-dimensional NMR

inferredcites →https://doi.org/10.1039/p29870000341openalex-snapshot

Two-dimensional nuclear magnetic resonance of sesquiterpenes. Part 2. Total assignment of (+)-aromadendrene, (+)-longicyclene, and γ-gurjunene by the two-dimensional INADEQUATE method

inferredcites →https://doi.org/10.1063/1.432450openalex-snapshot

Two-dimensional spectroscopy. Application to nuclear magnetic resonance

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.2020.112495zenodo-depositor-declared

Dimeric and esterified sesquiterpenes from the liverwort Chiastocaulon caledonicum

inferred← citeshttps://doi.org/10.1002/cbdv.201200122openalex-snapshot

Terpenes from the Soft Corals of the Genus Sarcophyton: Chemistry and Biological Activities

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Biomimetic Synthesis of (+)‐Ledene, (+)‐Viridiflorol, (−)‐Palustrol, (+)‐Spathulenol, and Psiguadial A, C, and D via the Platform Terpene (+)‐Bicyclogermacrene

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Reduction of cis‐ and trans‐1,2‐epithio‐p‐menth‐8‐ene: preparation of new fragrant terpenoid thiols

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Volatile oils from leaves and stem barks of Cedrela ﬁssilis (Meliaceae): chemical composition and antibacterial activities

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Two‐dimensional NMR of sesquiterpenes. 8—complete assignment of 1H and 13C NMR spectra of seven sequiterpene alcohols from Neocallitropsis pancheri

inferred← citeshttps://doi.org/10.1002/mrc.1291openalex-snapshot

Complete NMR assignment of (+)‐10β,14‐dihydroxy‐allo‐aromadendrane

inferred← citeshttps://doi.org/10.1007/bf02496189openalex-snapshot

(+)-Globulol as a new sesquiterpene alcohol fromAngelica sylvestris L.

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A new prenylated benzoquinone from Cyathocalyx pruniferus abrogates LPS-induced inflammatory responses associated with PGE2, COX-2 and cytokines biosynthesis in human plasma

inferred← citeshttps://doi.org/10.1016/0031-9422(93)85432-qopenalex-snapshot

β-Acoradienol, a sesquiterpene alcohol from Neocallitropsis pancheri

inferred← citeshttps://doi.org/10.1016/0031-9422(95)00079-8openalex-snapshot

Two guaiane and eudesmane-type sesquiterpenoids from Neocallitropsis pancheri

inferred← citeshttps://doi.org/10.1016/0031-9422(95)00938-8openalex-snapshot

(−)-Ledol from the liverwort Cephaloziella recurvifolia and the clarification of its identity

inferred← citeshttps://doi.org/10.1016/0031-9422(96)00105-7openalex-snapshot

Sesquiterpenoids from the liverworts Bazzania trilobata and Porella canariensis

inferred← citeshttps://doi.org/10.1016/0584-8539(95)01652-xopenalex-snapshot

Structural analysis of 10,11-dihydro-5,10-ethano-5H-dibenzo[a,d]cycloheptene. Partial 1H and 13C assignments using one- and two-dimensional NMR and determination of molecular conformation by the AM1 MO method

inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107144openalex-snapshot

Aromadendrane and alloaromedendrane-type sesquiterpenoids from the roots and rhizomes of Valeriana officinalis var. latifolia and their biological activities

inferred← citeshttps://doi.org/10.1016/j.indcrop.2015.07.044openalex-snapshot

Chemical composition of essential oils extracted from six Murraya species and their repellent activity against Tribolium castaneum

inferred← citeshttps://doi.org/10.1016/j.jep.2010.07.054openalex-snapshot

Activation of the nuclear receptor PPARγ by metabolites isolated from sage (Salvia officinalis L.)

inferred← citeshttps://doi.org/10.1016/j.mcat.2020.111264openalex-snapshot

Catalytic transformations of (+)-aromadendrene: Functionalization and isomerization reactions in the presence of the heteropoly acid catalyst H3PW12O40

inferred← citeshttps://doi.org/10.1016/j.phytochem.2003.08.021openalex-snapshot

Secondary metabolites from the liverwort Tylimanthus renifolius

inferred← citeshttps://doi.org/10.1016/j.phytochem.2008.08.025openalex-snapshot

Silvaglins and related 2,3-secodammarane derivatives – unusual types of triterpenes from Aglaia silvestris

inferred← citeshttps://doi.org/10.1016/j.phytochem.2015.08.011openalex-snapshot

Aromadendrane and cyclofarnesane sesquiterpenoids from cultures of the basidiomycete Inonotus sp. BCC 23706

inferred← citeshttps://doi.org/10.1016/j.tet.2004.08.027openalex-snapshot

Kunzeanones A, B, and C: novel alkylated phloroglucinol metabolites from Kunzea ambigua

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Spectrometric identifications of sesquiterpene alcohols from niaouli ( Melaleuca quinquenervia ) essential oil

inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00291-0openalex-snapshot

The stereochemistry of ledol from Renealmia chrysotrycha : an NMR study

inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00302-2openalex-snapshot

Terpenes from leaves of Guarea macrophylla (Meliaceae)

inferred← citeshttps://doi.org/10.1016/s0031-9422(00)89522-9openalex-snapshot

Biotransformation of sesquiterpenoids, (−)-globulol and (+)-ledol by Glomerella cingulata

inferred← citeshttps://doi.org/10.1016/s0031-9422(98)00283-0openalex-snapshot

Sesquiterpene constituents of the liverwort Calypogeia muelleriana

inferred← citeshttps://doi.org/10.1016/s0031-9422(98)00768-7openalex-snapshot

Two aromadendrane type alcohols from the liverwort Conocephalum conicum

inferred← citeshttps://doi.org/10.1016/s0031-9422(99)00470-7openalex-snapshot

Two 6,7-seco-caryophyllenes and an alloaromadendrane from liquid cultures of Hebeloma longicaudum

inferred← citeshttps://doi.org/10.1016/s0066-4103(08)60026-5openalex-snapshot

One-Bond 13C-13C Spin-Spin Coupling Constants

inferred← citeshttps://doi.org/10.1016/s0926-2040(02)00017-6openalex-snapshot

Carbon-13 CP-MAS nuclear magnetic resonance studies of teas

inferred← citeshttps://doi.org/10.1021/jf00037a024openalex-snapshot

Structure elucidation of oxidation-reduction products of isolongifolene

inferred← citeshttps://doi.org/10.1021/jf950052lopenalex-snapshot

Sesquiterpenic Epoxides and Alcohols Derived from Hydrocarbons of Vetiver Essential Oil

inferred← citeshttps://doi.org/10.1021/jf950706qopenalex-snapshot

Sesquiterpene Epoxidation: Rearrangement of (+)-Ledene Epoxy Compounds

inferred← citeshttps://doi.org/10.1021/jf960335topenalex-snapshot

Syntheses of Sesquiterpene Epoxides and Alcohols from γ-Gurjunene

inferred← citeshttps://doi.org/10.1021/jm3007454openalex-snapshot

Potent HGF/c-Met Axis Inhibitors from Eucalyptus globulus: the Coupling of Phloroglucinol and Sesquiterpenoid Is Essential for the Activity

inferred← citeshttps://doi.org/10.1021/np030490jopenalex-snapshot

Further Labdane and Kaurane Diterpenoids and Other Constituents from Plectranthus fruticosus

inferred← citeshttps://doi.org/10.1021/np9606052openalex-snapshot

A New Norlupene from the Leaves ofMelaleucaleucadendron

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Chemistry of Leichhardt's Grasshopper, Petasida ephippigera, and its Host Plants, Pityrodia jamesii, P. ternifolia, and P. pungens

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A stable cis-azobenzene in aqueous solution

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Reliable analysis of volatile compounds from small samples of Eucalyptus magnificata (Myrtaceae)

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Chemical Composition of Essential Oils from Cladodes and Inflorescences from Male and Female Specimens ofBaccharis milleflora

inferred← citeshttps://doi.org/10.1080/10412905.1997.10554251openalex-snapshot

Sesquiterpenes from Patchouli ( Pogostemon cablin ) Essential Oil. Assignment of the Proton and Carbon-13 NMR Spectra

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Aduncamide, a Cytotoxic and Antibacterial b-Phenylethylamine-Derived Amide fromPiper aduncum

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Chemical characterisation of the essential oils of three Baccharis species: Baccharis pentodonta Malme, Baccharis tridentata Vahl, and Baccharis linearifolia Pers

inferred← citeshttps://doi.org/10.1177/1934578x0700200201openalex-snapshot

Antiproliferative Sesquiterpenes from the Red Sea Soft Coral Sarcophyton Glaucum

inferred← citeshttps://doi.org/10.1515/znc-2015-0228openalex-snapshot

Isolation, antimicrobial and antitumor activities of a new polyhydroxysteroid and a new diterpenoid from the soft coral Xenia umbellata

inferred← citeshttps://doi.org/10.1590/1414-431x20133013openalex-snapshot

Sedative and anesthetic activities of the essential oils of Hyptis mutabilis (Rich.) Briq. and their isolated components in silver catfish (Rhamdia quelen)

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Antifouling Activity of Halogenated Compounds Derived from the Red Alga Sphaerococcus coronopifolius: Potential for the Development of Environmentally Friendly Solutions

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Phytochemical Study of the Ecuadorian Species Lepechinia mutica (Benth.) Epling and High Antifungal Activity of Carnosol against Pyricularia oryzae

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