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Diterpenoids of terrestrial origin

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

inferredcites →https://doi.org/10.1002/anie.201700565openalex-snapshot

Discovery and Characterization of a New Family of Diterpene Cyclases in Bacteria and Fungi

inferredcites →https://doi.org/10.1002/anie.201704929openalex-snapshot

Diastereoselective Total Synthesis of the Euphorbia Diterpenoid Pepluanol A: A Reductive Annulation Approach

inferredcites →https://doi.org/10.1002/cbdv.201600423openalex-snapshot

Diterpenoids from Wedelia prostrata and Their Derivatives and Cytotoxic Activities

inferredcites →https://doi.org/10.1002/cbdv.201600426openalex-snapshot

A New Depigmenting‐Antifungal Methylated Grindelane from Grindelia chiloensis

inferredcites →https://doi.org/10.1002/cbdv.201700327openalex-snapshot

New Bioactive Macrocyclic Diterpenoids from Euphorbia helioscopia

inferredcites →https://doi.org/10.1002/cbic.201700462openalex-snapshot

Harzianone Biosynthesis by the Biocontrol Fungus Trichoderma

inferredcites →https://doi.org/10.1002/ejoc.201700795openalex-snapshot

Aphapolins A and B: Two Nemoralisin Diterpenoids Isolated from Aphanamixis polystachya (Wall.) R. Parker

inferredcites →https://doi.org/10.1002/pca.2703openalex-snapshot

Screening of Hallucinogenic Compounds and Genomic Characterisation of 40 Anatolian Salvia Species

inferredcites →https://doi.org/10.1002/ptr.5749openalex-snapshot

Diterpenes as lead molecules against neglected tropical diseases

inferredcites →https://doi.org/10.1002/ptr.5800openalex-snapshot

Diterpenes and Their Derivatives as Potential Anticancer Agents

inferredcites →https://doi.org/10.1002/tcr.201600096openalex-snapshot

Divergent Total Synthesis of Atisane‐Type Diterpenoids

inferredcites →https://doi.org/10.1007/7355_2014_81openalex-snapshot

Medicinal Chemistry of Plant Naturals as Agonists/Antagonists for Taste Receptors

inferredcites →https://doi.org/10.1007/s11101-016-9478-9openalex-snapshot

Anticancer potential of labdane diterpenoid lactone “andrographolide” and its derivatives: a semi-synthetic approach

inferredcites →https://doi.org/10.1007/s11101-017-9494-4openalex-snapshot

Bioactive diterpenoids from Celastraceae species

inferredcites →https://doi.org/10.1016/b978-0-444-63929-5.00004-8openalex-snapshot

Antibacterial Potential of Diterpenoids

inferredcites →https://doi.org/10.1016/b978-0-444-63929-5.00005-xopenalex-snapshot

Chemistry and Bioactivity of ent -Kaurene Diterpenoids

inferredcites →https://doi.org/10.1016/b978-0-444-63930-1.00001-6openalex-snapshot

Pharmacology and Structure-Activity Relationship of Natural Products With Psychoactive Effects From Salvia divinorum, Mitragyna speciosa, and Ayahuasca

inferredcites →https://doi.org/10.1016/j.bioorg.2017.07.013openalex-snapshot

Novel dehydroabietylamine derivatives as potent inhibitors of acetylcholinesterase

inferredcites →https://doi.org/10.1016/j.bioorg.2017.08.008openalex-snapshot

Phytochemicals with NO inhibitory effects and interactions with iNOS protein from Trigonostemon howii

inferredcites →https://doi.org/10.1016/j.bioorg.2017.09.007openalex-snapshot

Nitric oxide inhibitory daphnane diterpenoids as potential anti-neuroinflammatory agents for AD from the twigs of Trigonostemon thyrsoideus

inferredcites →https://doi.org/10.1016/j.biopha.2017.08.069openalex-snapshot

Rosoloactone: A natural diterpenoid inducing apoptosis in human cervical cancer cells through endoplasmic reticulum stress and mitochondrial damage

inferredcites →https://doi.org/10.1016/j.bmc.2016.10.019openalex-snapshot

Antibacterial profiling of abietane-type diterpenoids

inferredcites →https://doi.org/10.1016/j.bmcl.2016.11.044openalex-snapshot

Natural NO inhibitors from the leaves of Callicarpa kwangtungensis: Structures, activities, and interactions with iNOS

inferredcites →https://doi.org/10.1016/j.bmcl.2016.11.063openalex-snapshot

Phytochemical and cytotoxic studies on the roots of Euphorbia fischeriana

inferredcites →https://doi.org/10.1016/j.bmcl.2016.12.032openalex-snapshot

Identification of a diverse synthetic abietane diterpenoid library for anticancer activity

inferredcites →https://doi.org/10.1016/j.bmcl.2017.01.055openalex-snapshot

Cytotoxic clerodane diterpenoids from Croton crassifolius

inferredcites →https://doi.org/10.1016/j.bmcl.2017.02.051openalex-snapshot

Isolation and characterization of diterpene glycosides from Siegesbeckia pubescens

inferredcites →https://doi.org/10.1016/j.bmcl.2017.05.006openalex-snapshot

Cytotoxic and apoptosis-inducing activities against human lung cancer cell lines of cassaine diterpenoids from the bark of Erythrophleum fordii

inferredcites →https://doi.org/10.1016/j.bmcl.2017.07.039openalex-snapshot

Synthesis of antimalarial amide analogues based on the plant serrulatane diterpenoid 3,7,8-trihydroxyserrulat-14-en-19-oic acid

inferredcites →https://doi.org/10.1016/j.bmcl.2017.08.033openalex-snapshot

Synthesis of novel forskolin isoxazole derivatives with potent anti-cancer activity against breast cancer cell lines

inferredcites →https://doi.org/10.1016/j.bmcl.2017.10.063openalex-snapshot

Synthesis of 14-deoxy-11,12-didehydroandrographolide analogues as potential cytotoxic agents for cholangiocarcinoma

inferredcites →https://doi.org/10.1016/j.bmcl.2017.11.001openalex-snapshot

Aspergillus candidus is a newly recognized source of sphaeropsidin A: Isolation, semi-synthetic derivatization and anticancer evaluation

inferredcites →https://doi.org/10.1016/j.bmcl.2017.11.014openalex-snapshot

Identification of a diverse synthetic abietane diterpenoid library and insight into the structure-activity relationships for antibacterial activity

inferredcites →https://doi.org/10.1016/j.bse.2017.09.001openalex-snapshot

Mannic acid, a new ent -kaurane dimer diterpenoid and other chemical constituents from different parts of Diospyros mannii

inferredcites →https://doi.org/10.1016/j.cclet.2017.02.020openalex-snapshot

Three new dimeric diterpenes from Rhododendron molle

inferredcites →https://doi.org/10.1016/j.fct.2017.03.026openalex-snapshot

Echinodorus grandiflorus: Ethnobotanical, phytochemical and pharmacological overview of a medicinal plant used in Brazil

inferredcites →https://doi.org/10.1016/j.fitote.2016.11.018openalex-snapshot

Sauruchinenols A and B, unprecedented monocyclic diterpenes with new carbon skeleton from the aerial parts of Saururus chinensis

inferredcites →https://doi.org/10.1016/j.fitote.2017.01.013openalex-snapshot

New terpenoids from Resina Commiphora

inferredcites →https://doi.org/10.1016/j.fitote.2017.03.006openalex-snapshot

Monomeric and dimeric ent-kauranoid-type diterpenoids from rabdosia japonica and their cytotoxicity and anti-HBV activities

inferredcites →https://doi.org/10.1016/j.fitote.2017.03.012openalex-snapshot

Scubatines A–F, new cytotoxic neo -clerodane diterpenoids from Scutellaria barbata D. Don

inferredcites →https://doi.org/10.1016/j.fitote.2017.06.001openalex-snapshot

Three new abietane-type diterpene glycosides from the roots of Tripterygium wilfordii

inferredcites →https://doi.org/10.1016/j.fitote.2017.06.006openalex-snapshot

Diterpenoids with diverse scaffolds from Vitex trifolia as potential topoisomerase I inhibitor

inferredcites →https://doi.org/10.1016/j.fitote.2017.08.006openalex-snapshot

Labdane diterpenoids from Curcuma amada rhizomes collected in Myanmar and their antiproliferative activities

inferredcites →https://doi.org/10.1016/j.fitote.2017.08.016openalex-snapshot

Abietane diterpenoids from Sideritis montana L. and their antiproliferative activity

inferredcites →https://doi.org/10.1016/j.fitote.2017.09.013openalex-snapshot

New neo -clerodane diterpenoids with neurotrophic activity from the aerial parts of Salvia tiliifolia

inferredcites →https://doi.org/10.1016/j.molstruc.2017.06.040openalex-snapshot

Determination of absolute configuration of an isopimarane-type diterpenoid by experimental and theoretical electronic circular dichroism and vibrational circular dichroism

inferredcites →https://doi.org/10.1016/j.orggeochem.2017.08.013openalex-snapshot

Identification of 15-nor-cleroda-3,12-diene in a Dominican amber

inferredcites →https://doi.org/10.1016/j.phrs.2017.07.019openalex-snapshot

Labdane diterpenoids as potential anti-inflammatory agents

inferredcites →https://doi.org/10.1016/j.phytochem.2016.10.008openalex-snapshot

Bioactive constituents from transformed root cultures of Nepeta teydea

inferredcites →https://doi.org/10.1016/j.phytochem.2016.10.010openalex-snapshot

A grayanotox-9(11)-ene derivative from Rhododendron brachycarpum and its structural assignment via a protocol combining NMR and DP4 plus application

inferredcites →https://doi.org/10.1016/j.phytochem.2016.10.012openalex-snapshot

Selective in vitro and in silico butyrylcholinesterase inhibitory activity of diterpenes and rosmarinic acid isolated from Perovskia atriplicifolia Benth. and Salvia glutinosa L.

inferredcites →https://doi.org/10.1016/j.phytochem.2016.12.001openalex-snapshot

Rebaudiosides T and U, minor C-19 xylopyranosyl and arabinopyranosyl steviol glycoside derivatives from Stevia rebaudiana (Bertoni) Bertoni

inferredcites →https://doi.org/10.1016/j.phytochem.2016.12.008openalex-snapshot

Bioactive isopimarane diterpenoids from the stems of Euonymus oblongifolius

inferredcites →https://doi.org/10.1016/j.phytochem.2016.12.021openalex-snapshot

Chemical profile and defensive function of the latex of Euphorbia peplus

inferredcites →https://doi.org/10.1016/j.phytochem.2017.01.009openalex-snapshot

Deheiculatins A-L, 20-oxygenated cembranoids from Macaranga deheiculata

inferredcites →https://doi.org/10.1016/j.phytochem.2017.02.001openalex-snapshot

A unique natural selective kappa -opioid receptor agonist, salvinorin A, and its roles in human therapeutics

inferredcites →https://doi.org/10.1016/j.phytochem.2017.02.005openalex-snapshot

Chemical constituents of Pholidota cantonensis

inferredcites →https://doi.org/10.1016/j.phytochem.2017.02.021openalex-snapshot

Anti-inflammatory ent -kaurenoic acids and their glycosides from Gochnatia decora

inferredcites →https://doi.org/10.1016/j.phytochem.2017.07.008openalex-snapshot

Roscotanes and roscoranes: Oxygenated abietane and pimarane diterpenoids from Kaempferia roscoeana

inferredcites →https://doi.org/10.1016/j.phytochem.2017.08.009openalex-snapshot

Bioactive ent-kaurane diterpenoids from Isodon rubescens

inferredcites →https://doi.org/10.1016/j.phytochem.2017.08.014openalex-snapshot

Diterpenoids from the roots of Croton dichogamus Pax

inferredcites →https://doi.org/10.1016/j.phytochem.2017.09.003openalex-snapshot

Bioactive diterpenoids from Croton laevigatus

inferredcites →https://doi.org/10.1016/j.phytochem.2017.09.005openalex-snapshot

Clerodane diterpenoids from Scutellaria formosana with inhibitory effects on NO production and interactions with iNOS protein

inferredcites →https://doi.org/10.1016/j.phytol.2016.10.020openalex-snapshot

Neoclerodane diterpenoids from aerial parts of Scutellaria barbata

inferredcites →https://doi.org/10.1016/j.phytol.2016.11.008openalex-snapshot

Three new abietane-type diterpenes from the bark of Cryptomeria japonica

inferredcites →https://doi.org/10.1016/j.phytol.2016.11.010openalex-snapshot

Three new labdane diterpenes from Loxocalyx urticifolius

inferredcites →https://doi.org/10.1016/j.phytol.2016.12.013openalex-snapshot

Two new labdane diterpenoids and one new β-lactam from the aerial parts of Roylea cinerea

inferredcites →https://doi.org/10.1016/j.phytol.2017.02.001openalex-snapshot

Plebeins A-F, sesquiterpenoids and diterpenoids from Salvia plebeian

inferredcites →https://doi.org/10.1016/j.phytol.2017.03.007openalex-snapshot

Two new diterpenoids from Aleuritopteris argentea

inferredcites →https://doi.org/10.1016/j.phytol.2017.04.002openalex-snapshot

Novel labdane diterpenoids from the aerial parts of Leonurus japonicus

inferredcites →https://doi.org/10.1016/j.phytol.2017.04.018openalex-snapshot

Eudesmanolide sesquiterpenes and protein tyrosine phosphatase 1B inhibitory ent -kaurene diterpenes from aerial parts of Indonesian Wedelia prostata

inferredcites →https://doi.org/10.1016/j.phytol.2017.04.025openalex-snapshot

New tetranorlabdane diterpenoids from the fruits of Elettaria cardamomum Maton

inferredcites →https://doi.org/10.1016/j.phytol.2017.04.029openalex-snapshot

Four new ent -kaurene diterpene glucosides from Mikania micrantha

inferredcites →https://doi.org/10.1016/j.phytol.2017.05.001openalex-snapshot

Two new labdane diterpenoids from the foliar exudates of Blakiella bartsiifolia

inferredcites →https://doi.org/10.1016/j.phytol.2017.05.006openalex-snapshot

Diterpenoids from the needles and twigs of the cultivated endangered pine Pinus kwangtungensis and their PTP1B inhibitory effects

inferredcites →https://doi.org/10.1016/j.phytol.2017.05.018openalex-snapshot

Three new dolabrane diterpenes from the Chinese mangrove plant of Ceriops tagal

inferredcites →https://doi.org/10.1016/j.phytol.2017.06.019openalex-snapshot

Ent -kaurene diterpenoids and lignan from Leontopodium leontopodioides and their inhibitory activities against cyclooxygenases-1 and 2

inferredcites →https://doi.org/10.1016/j.phytol.2017.07.003openalex-snapshot

New ent -kaurane and ent -pimarane diterpenoids from Siegesbeckia pubescens

inferredcites →https://doi.org/10.1016/j.phytol.2017.07.011openalex-snapshot

Anti-inflammatory abietane diterpenoids from the seeds of Podocarpus nagi

inferredcites →https://doi.org/10.1016/j.phytol.2017.07.016openalex-snapshot

New cassane diterpenes from the fruits of Caesalpinia mimosoides Lam.

inferredcites →https://doi.org/10.1016/j.phytol.2017.09.003openalex-snapshot

Two new sesquarterpenoids from the bark of Cryptomeria japonica

inferredcites →https://doi.org/10.1016/j.phytol.2017.09.007openalex-snapshot

Bioactive cassane diterpenoids from the seeds of Caesalpinia sappan

inferredcites →https://doi.org/10.1016/j.phytol.2017.09.023openalex-snapshot

Labdane and norlabdane diterpenoids from the aerial parts of Leonurus japonicus

inferredcites →https://doi.org/10.1016/j.phytol.2017.10.007openalex-snapshot

Cytotoxic abietane-type diterpenoids from twigs and leaves of Croton laevigatus

inferredcites →https://doi.org/10.1016/j.phytol.2017.10.010openalex-snapshot

Isopimarane-type diterpenoids from Callicarpa macrophylla vahl

inferredcites →https://doi.org/10.1016/j.tet.2016.12.060openalex-snapshot

Isopimarane and nor-diterpene glucosides from the twigs and leaves of Lyonia ovalifolia

inferredcites →https://doi.org/10.1016/j.tet.2017.02.006openalex-snapshot

Terpenoids with potent antimycobacterial activity against Mycobacterium tuberculosis from Trigonostemon reidioides roots

inferredcites →https://doi.org/10.1016/j.tet.2017.02.032openalex-snapshot

Synthesis of derivatives of podocarpane-type diterpenoids through Diels-Alder cycloaddition and photo-decarbonylation from unmasked ortho-benzoquinone

inferredcites →https://doi.org/10.1016/j.tet.2017.04.015openalex-snapshot

Cytotoxic labdane diterpenes and bisflavonoid atropisomers from leaves of Araucaria bidwillii

inferredcites →https://doi.org/10.1016/j.tet.2017.07.021openalex-snapshot

Two novel diterpenes from the roots of Phyllanthus acidus (L.) Skeel

inferredcites →https://doi.org/10.1016/j.tet.2017.10.061openalex-snapshot

Oxazonigelladine and dolabellane-type diterpene constituents from Nigella damascena seeds

inferredcites →https://doi.org/10.1016/j.tet.2017.11.002openalex-snapshot

Microbial oxidation of harzianone by Bacillus sp. IMM-006

inferredcites →https://doi.org/10.1016/j.tetasy.2016.11.006openalex-snapshot

Absolute configuration of diterpenoids from Jatropha dioica by vibrational circular dichroism

inferredcites →https://doi.org/10.1016/j.tetlet.2016.12.029openalex-snapshot

Vulgarisins B–D, three novel diterpenoids with a rare skeleton isolated from Prunella vulgaris Linn

inferredcites →https://doi.org/10.1016/j.tetlet.2016.12.034openalex-snapshot

ent-Kaurene diterpenoids from Isodon phyllostachys

inferredcites →https://doi.org/10.1016/j.tetlet.2017.01.085openalex-snapshot

Facile synthesis and structural characterization of μ4-oxo tetrazinc clusters of beyerenoic and kaurenoic acids

inferredcites →https://doi.org/10.1016/j.tetlet.2017.02.010openalex-snapshot

Total synthesis of natural fregenedadiol and its diacetate, rearranged labdanes with aromatized B ring

inferredcites →https://doi.org/10.1016/j.tetlet.2017.02.078openalex-snapshot

A convenient method for the preparation of 20-[ 18 O]-labeled ingenol

inferredcites →https://doi.org/10.1016/j.tetlet.2017.03.052openalex-snapshot

Secondary metabolites of the lichen-associated fungus Apiospora montagnei

inferredcites →https://doi.org/10.1016/j.tetlet.2017.03.072openalex-snapshot

First total synthesis of (−)-salprzelactone

inferredcites →https://doi.org/10.1016/j.tetlet.2017.03.078openalex-snapshot

Site-selective Csp 3 -H aryloxylation of natural product Tanshinone IIA and its analogues

inferredcites →https://doi.org/10.1016/j.tetlet.2017.04.081openalex-snapshot

Diterpenes with new isoryanodane derived skeletons from Persea indica

inferredcites →https://doi.org/10.1016/j.tetlet.2017.06.030openalex-snapshot

Epoxy lactones by photooxidative rearrangement of 6β-acetoxyvouacapane

inferredcites →https://doi.org/10.1016/j.tetlet.2017.07.106openalex-snapshot

Antimutagenic activity of ent-kaurane diterpenoids from the aerial parts of Isodon japonicus

inferredcites →https://doi.org/10.1016/j.tetlet.2017.08.055openalex-snapshot

Boesenberols I–K, new isopimarane diterpenes from Boesenbergia pandurata with TRAIL-resistance overcoming activity

inferredcites →https://doi.org/10.1016/j.tetlet.2017.08.073openalex-snapshot

Two ring opened oxetane taxoids containing a C-20 benzoyloxy group from the roots of Taxus wallichiana Zucc.

inferredcites →https://doi.org/10.1016/j.tetlet.2017.11.012openalex-snapshot

Corroborating study on the absolute configurations of trigochinins A–C

inferredcites →https://doi.org/10.1021/acs.jafc.6b05159openalex-snapshot

Methyl and p-Bromobenzyl Esters of Hydrogenated Kaurenoic Acid for Controlling Anthracnose in Common Bean Plants

inferredcites →https://doi.org/10.1021/acs.jafc.6b05376openalex-snapshot

Novel ent-Kaurane Diterpenoid from Rubus corchorifolius L. f. Inhibits Human Colon Cancer Cell Growth via Inducing Cell Cycle Arrest and Apoptosis

inferredcites →https://doi.org/10.1021/acs.jafc.6b05793openalex-snapshot

Development and Validation of an Enzymatic Method To Determine Stevioside Content from Stevia rebaudiana

inferredcites →https://doi.org/10.1021/acs.jafc.7b01500openalex-snapshot

Highly Oxygenated Grayanane Diterpenoids from Flowers of Pieris japonica and Structure–Activity Relationships of Antifeedant Activity against Pieris brassicae

inferredcites →https://doi.org/10.1021/acs.jafc.7b02384openalex-snapshot

Diterpenoids from Salvia miltiorrhiza and Their Immune-Modulating Activity

inferredcites →https://doi.org/10.1021/acs.jafc.7b03461openalex-snapshot

Structural Diversity and Biological Activity of the Genus Pieris Terpenoids

inferredcites →https://doi.org/10.1021/acs.jmedchem.7b00148openalex-snapshot

Addressing Structural Flexibility at the A-Ring on Salvinorin A: Discovery of a Potent Kappa-Opioid Agonist with Enhanced Metabolic Stability

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00150openalex-snapshot

ent-Strobane andent-Pimarane Diterpenoids fromSiegesbeckia pubescens

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00425openalex-snapshot

Crassins A–H, Diterpenoids from the Roots of Croton crassifolius

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00676openalex-snapshot

Cytotoxic Fusicoccane-Type Diterpenoids from Streptomyces violascens Isolated from Ailuropoda melanoleuca Feces

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00700openalex-snapshot

Antiproliferative Activity of Natural Taiwaniaquinoids and Related Compounds

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00764openalex-snapshot

Probing Labdane-Related Diterpenoid Biosynthesis in the Fungal Genus Aspergillus

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00786openalex-snapshot

ent-Abietane and Tigliane Diterpenoids from the Roots of Euphorbia fischeriana and Their Inhibitory Effects against Mycobacterium smegmatis

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00802openalex-snapshot

Diterpenoids and Lignans from Cephalotaxus fortunei

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00972openalex-snapshot

Nepetaefolins A–J, Cytotoxic Chinane and Abietane Diterpenoids from Caryopteris nepetaefolia

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00976openalex-snapshot

Clerodane Diterpenoid Glucosides from the Stems of Tinospora sinensis

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01053openalex-snapshot

Antibacterial and Hypoglycemic Diterpenoids from Salvia chamaedryoides

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01084openalex-snapshot

Exploring Jolkinol D Derivatives To Overcome Multidrug Resistance in Cancer

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01096openalex-snapshot

Inflammation Modulatory Phorbol Esters from the Seeds of Aquilaria malaccensis

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01099openalex-snapshot

Terpenoids from Euphorbia soongarica and Their Multidrug Resistance Reversal Activity

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01100openalex-snapshot

Sesqui- and Diterpenoids from the Radix of Curcuma aromatica

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01141openalex-snapshot

Chemical Constituents and Anti-inflammatory Principles from the Fruits of Forsythia suspensa

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01151openalex-snapshot

Corymbulosins D–H, 2-Hydroxy- and 2-Oxo-clerodane Diterpenes from the Bark of Laetia corymbulosa

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01195openalex-snapshot

Vitepyrroloids A–D, 2-Cyanopyrrole-Containing Labdane Diterpenoid Alkaloids from the Leaves of Vitex trifolia

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01196openalex-snapshot

Botrysphones A–C and Botrysphins A–F, Triketides and Diterpenoids from the Fungus Botrysphaeria laricina

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00006openalex-snapshot

α-Glucosidase Inhibitory and Cytotoxic Taxane Diterpenoids from the Stem Bark of Taxus wallichiana

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00057openalex-snapshot

6,7-Seco- ent -Kauranoids Derived from Oridonin as Potential Anticancer Agents

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00113openalex-snapshot

Environmentally Friendly Procedure Based on Supercritical Fluid Chromatography and Tandem Mass Spectrometry Molecular Networking for the Discovery of Potent Antiviral Compounds from Euphorbia semiperfoliata

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00155openalex-snapshot

α-Glucosidase Inhibitors from Salvia circinata

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00163openalex-snapshot

Structurally Diverse Diterpenoids from Isodon scoparius and Their Bioactivity

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00188openalex-snapshot

Neoclerodane Diterpenoids from Reehal Fatima, Teucrium yemense

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00193openalex-snapshot

Stereochemistry of a Second Riolozane and Other Diterpenoids from Jatropha dioica

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00198openalex-snapshot

Isolation, Structure Elucidition, and Immunosuppressive Activity of Diterpenoids from Ligularia fischeri

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00233openalex-snapshot

Isolation of Premyrsinane, Myrsinane, and Tigliane Diterpenoids from Euphorbia pithyusa Using a Chikungunya Virus Cell-Based Assay and Analogue Annotation by Molecular Networking

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00238openalex-snapshot

Total Synthesis of Tanshinone I

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00249openalex-snapshot

Sucupiranins A–L, Furanocassane Diterpenoids from the Seeds of Bowdichia virgilioides

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00324openalex-snapshot

Bistinospinosides A and B, Dimeric Clerodane Diterpene Glycosides from Tinospora sagittata

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00327openalex-snapshot

Semisynthesis and Kappa-Opioid Receptor Activity of Derivatives of Columbin, a Furanolactone Diterpene

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00332openalex-snapshot

Gaditanone, a Diterpenoid Based on an Unprecedented Carbon Skeleton Isolated from Euphorbia gaditana

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00347openalex-snapshot

Norditerpenoids and Dinorditerpenoids from the Seeds of Podocarpus nagi as Cytotoxic Agents and Autophagy Inducers

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00365openalex-snapshot

Borapetoside E, a Clerodane Diterpenoid Extracted fromTinospora crispa, Improves Hyperglycemia and Hyperlipidemia in High-Fat-Diet-Induced Type 2 Diabetes Mice

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00395openalex-snapshot

Cafestol, a Bioactive Substance in Coffee, Has Antidiabetic Properties in KKAy Mice

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00412openalex-snapshot

Cephanolides A–J, Cephalotane-Type Diterpenoids from Cephalotaxus sinensis

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00591openalex-snapshot

neo-Clerodane Diterpenoids from Salvia polystachya Stimulate the Expression of Extracellular Matrix Components in Human Dermal Fibroblasts

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00595openalex-snapshot

Heterodimeric Diterpenoids Isolated fromEuphorbia ebracteolataRoots and Their Inhibitory Effects on α-Glucosidase

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00659openalex-snapshot

Oxazole-Containing Diterpenoids from Cell Cultures of Salvia miltiorrhiza and Their Anti-HIV-1 Activities

inferredcites →https://doi.org/10.1021/acs.orglett.6b03597openalex-snapshot

Taxodikaloids A and B, Two Dimeric Abietane-Type Diterpenoids from Taxodium ascendens Possessing an Oxazoline Ring Linkage

inferredcites →https://doi.org/10.1021/acs.orglett.7b00048openalex-snapshot

Pierisketolide A and Pierisketones B and C, Three Diterpenes with an Unusual Carbon Skeleton from the Roots of Pieris formosa

inferredcites →https://doi.org/10.1021/acs.orglett.7b00204openalex-snapshot

Two Furanharzianones with 4/7/5/6/5 Ring System from Microbial Transformation of Harzianone

inferredcites →https://doi.org/10.1021/acs.orglett.7b00268openalex-snapshot

Palladium-Catalyzed α-Arylation of Cyclic Vinylogous Esters for the Synthesis of γ-Arylcyclohexenones and Total Synthesis of Aromatic Podocarpane Diterpenoids

inferredcites →https://doi.org/10.1021/acs.orglett.7b00918openalex-snapshot

Enantio- and Stereoselective Construction of Atisane Scaffold via Organocatalytic Intramolecular Michael Reaction and Diels–Alder Reaction

inferredcites →https://doi.org/10.1021/acs.orglett.7b01323openalex-snapshot

Cinnamomols A and B, Immunostimulative Diterpenoids with a New Carbon Skeleton from the Leaves of Cinnamomum cassia

inferredcites →https://doi.org/10.1021/acs.orglett.7b01813openalex-snapshot

Natural and Semisynthetic Tigliane Diterpenoids with New Carbon Skeletons from Euphorbia dracunculoides as a Wnt Signaling Pathway Inhibitor

inferredcites →https://doi.org/10.1021/acs.orglett.7b01863openalex-snapshot

Rhodomollanol A, a Highly Oxygenated Diterpenoid with a 5/7/5/5 Tetracyclic Carbon Skeleton from the Leaves of Rhododendron molle

inferredcites →https://doi.org/10.1021/acs.orglett.7b02633openalex-snapshot

Rhodomollacetals A–C, PTP1B Inhibitory Diterpenoids with a 2,3:5,6-Di-seco-grayanane Skeleton from the Leaves of Rhododendron molle

inferredcites →https://doi.org/10.1021/acs.orglett.7b02684openalex-snapshot

Modular Approach to pseudo-Neoclerodanes as Designer κ-Opioid Ligands

inferredcites →https://doi.org/10.1021/acscentsci.7b00488openalex-snapshot

Dynamic Strategic Bond Analysis Yields a Ten-Step Synthesis of 20-nor-Salvinorin A, a Potent κ-OR Agonist

inferredcites →https://doi.org/10.1021/jacs.7b00140openalex-snapshot

Convergent Route to ent -Kaurane Diterpenoids: Total Synthesis of Lungshengenin D and 1α,6α-Diacetoxy- ent -kaura-9(11),16-dien-12,15-dione

inferredcites →https://doi.org/10.1021/jacs.7b02746openalex-snapshot

Total Syntheses of Highly Oxidized ent -Kaurenoids Pharicin A, Pharicinin B, 7- O -Acetylpseurata C, and Pseurata C: A [5+2] Cascade Approach

inferredcites →https://doi.org/10.1021/jacs.7b10177openalex-snapshot

Total Synthesis of Resiniferatoxin Enabled by Radical-Mediated Three-Component Coupling and 7- endo Cyclization

inferredcites →https://doi.org/10.1038/s41598-017-04399-wopenalex-snapshot

Heliosterpenoids A and B, two Novel Jatrophane-Derived Diterpenoids with a 5/6/4/6 Ring System from Euphorbia helioscopia

inferredcites →https://doi.org/10.1039/c6np00124fopenalex-snapshot

Marine natural products

inferredcites →https://doi.org/10.1039/c7np00027hopenalex-snapshot

Diterpenoids from Isodon species: an update

inferredcites →https://doi.org/10.1039/c7np00033bopenalex-snapshot

Enabling syntheses of diterpenoid alkaloids and related diterpenes by an oxidative dearomatization/Diels–Alder cycloaddition strategy

inferredcites →https://doi.org/10.1039/c7np00040eopenalex-snapshot

Diterpenoids of terrestrial origin

inferredcites →https://doi.org/10.1039/c7ra08635kopenalex-snapshot

Biological and chemical guided isolation of 3,4-secograyanane diterpenoids from the roots of Pieris formosa

inferredcites →https://doi.org/10.1039/c7ra08877aopenalex-snapshot

ent-Rosane diterpenoids from Euphorbia milii showing an Epstein–Barr virus lytic replication assay

inferredcites →https://doi.org/10.1039/c7ra11982hopenalex-snapshot

Ent -abietane diterpenoids and their probable biogenetic precursors from the roots of Euphorbia fischeriana

inferredcites →https://doi.org/10.1055/s-0036-1588353openalex-snapshot

A Short and Improved Synthesis of the Antiprotozoal Abietane Diterpenoid (–)-Sugikurojin A

inferredcites →https://doi.org/10.1055/s-0042-115646openalex-snapshot

Antiparasitic Activity of Diterpenoids Against Trypanosoma cruzi

inferredcites →https://doi.org/10.1080/09168451.2017.1285689openalex-snapshot

Biochemical synthesis of uniformly 13C-labeled diterpene hydrocarbons and their bioconversion to diterpenoid phytoalexins in planta

inferredcites →https://doi.org/10.1080/10286020.2016.1232714openalex-snapshot

Isolation, structure elucidation, and induction of hepatoma cell apoptosis of abietane diterpenoids from Abies faxoniana

inferredcites →https://doi.org/10.1080/10286020.2016.1274307openalex-snapshot

Cytotoxic diterpenoids from Pteris ensiformis

inferredcites →https://doi.org/10.1080/10286020.2017.1307836openalex-snapshot

Phorbol ester-type diterpenoids from the twigs and leaves of Croton tiglium

inferredcites →https://doi.org/10.1080/14786419.2016.1188096openalex-snapshot

The roots of Salvia rhytidea: a rich source of biologically active diterpenoids

inferredcites →https://doi.org/10.1080/14786419.2016.1190723openalex-snapshot

Abietane diterpenes from the cones of Abies numidica de Lannoy ex Carrière (Pinaceae) and in vitro evaluation of their antimicrobial properties

inferredcites →https://doi.org/10.1080/14786419.2016.1222385openalex-snapshot

A new ent-kaurane diterpene from Euphorbia stracheyi Boiss

inferredcites →https://doi.org/10.1080/14786419.2016.1247078openalex-snapshot

Solanerioside A, an unusual 14,15-dinor-cyclophytane glucoside from the leaves of Solanum erianthum

inferredcites →https://doi.org/10.1080/14786419.2016.1250087openalex-snapshot

A new abietane mono-norditerpenoid from Podocarpus nagi

inferredcites →https://doi.org/10.1080/14786419.2016.1250088openalex-snapshot

Two new ent-atisane diterpenoids from the whole plants of Euphorbia wallichii

inferredcites →https://doi.org/10.1080/14786419.2016.1266350openalex-snapshot

Three new diterpenoids from Croton laui Merr. et Metc

inferredcites →https://doi.org/10.1080/14786419.2016.1269096openalex-snapshot

Phytochemical and biological evaluation of Salvia apiana

inferredcites →https://doi.org/10.1080/14786419.2017.1290614openalex-snapshot

Synthesis of a new allelopathic agent from the biotransformation of ent-15α-hydroxy-16-kauren-19-oic acid with Fusarium proliferatum

inferredcites →https://doi.org/10.1080/14786419.2017.1290619openalex-snapshot

A nor-diterpene from Salvia sahendica leaves

inferredcites →https://doi.org/10.1080/14786419.2017.1297441openalex-snapshot

Diterpenoids with thioredoxin reductase inhibitory activities from Jatropha multifida

inferredcites →https://doi.org/10.1080/14786419.2017.1305381openalex-snapshot

Taxanes from Taxus wallichiana var. mairei cultivated in the southern area of the Yangtze River in China

inferredcites →https://doi.org/10.1080/14786419.2017.1314280openalex-snapshot

Abietane diterpenoids from Cephalotaxus lanceolata

inferredcites →https://doi.org/10.1080/14786419.2017.1317775openalex-snapshot

Two new kaurane-type diterpenoids from Wedelia chinensis (Osbeck.) Merr

inferredcites →https://doi.org/10.1093/jxb/erw493openalex-snapshot

A (–)-kolavenyl diphosphate synthase catalyzes the first step of salvinorin A biosynthesis in Salvia divinorum

inferredcites →https://doi.org/10.1104/pp.15.01593openalex-snapshot

Integrative Approaches for the Identification and Localization of Specialized Metabolites in Tripterygium Roots

inferredcites →https://doi.org/10.1104/pp.17.00659openalex-snapshot

Biosynthesis of Diterpenoids in Tripterygium Adventitious Root Cultures

inferredcites →https://doi.org/10.1111/tpj.13427openalex-snapshot

Biosynthesis of the psychotropic plant diterpene salvinorin A: Discovery and characterization of the Salvia divinorum clerodienyl diphosphate synthase

inferredcites →https://doi.org/10.1248/cpb.c16-00775openalex-snapshot

A Novel Clerodane Diterpene from Vitex cofassus

showing the first 200 of 219 · page through all 219

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.2021.112659zenodo-depositor-declared

Aromatin D-J: Seven previously undescribed labdane diterpenoids isolated from Blumea aromatica

inferred← citeshttps://doi.org/10.1002/adsc.202300798openalex-snapshot

Functionalized Alkylidenecyclobutanes from a Cyclopent‐2‐enone Substrate via a Tandem Photochemical Transformation and an Allylic Substitution Protocol

inferred← citeshttps://doi.org/10.1002/ange.202009128openalex-snapshot

Divergent Total Synthesis of Euphoranginol C, Euphoranginone D, ent ‐Trachyloban‐3β‐ol, ent ‐Trachyloban‐3‐one, Excoecarin E, and ent ‐16α‐Hydroxy‐atisane‐3‐one

inferred← citeshttps://doi.org/10.1002/anie.202009128openalex-snapshot

Divergent Total Synthesis of Euphoranginol C, Euphoranginone D, ent ‐Trachyloban‐3β‐ol, ent ‐Trachyloban‐3‐one, Excoecarin E, and ent ‐16α‐Hydroxy‐atisane‐3‐one

inferred← citeshttps://doi.org/10.1002/cbdv.202300208openalex-snapshot

Synthesis and Evaluation of Piperazine‐Tethered Derivatives of Alepterolic Acid as Anticancer Agents

inferred← citeshttps://doi.org/10.1002/cbdv.202301676openalex-snapshot

Three New Clerodane Diterpenoids and Their NLRP3 Inflammasome Activation Inhibitory Activity from Callicarpa arborea Roxb

inferred← citeshttps://doi.org/10.1002/cbdv.202401706openalex-snapshot

Benzylpiperazinyl Derivatives of Alepterolic Acid: Synthesis and Cytotoxic Evaluation

inferred← citeshttps://doi.org/10.1002/cbdv.202403352openalex-snapshot

Natural Products in Cyperus Species (Cyperaceae): Phytochemistry, Pharmacological Activities, and Biosynthesis

inferred← citeshttps://doi.org/10.1002/med.21816openalex-snapshot

Recent progress and new perspectives for diterpenoid biosynthesis in medicinal plants

inferred← citeshttps://doi.org/10.1007/s11829-026-10264-3openalex-snapshot

Diversity of terpenoids in arthropod–plant interactions

inferred← citeshttps://doi.org/10.1016/j.amsu.2022.104125openalex-snapshot

Modern drug discovery applications for the identification of novel candidates for COVID-19 infections

inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.105759openalex-snapshot

Cytotoxic diterpenoid dimer containing an intricately caged core from Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109347openalex-snapshot

Casbane diterpenoids from Euphorbiaceae suppresse neuroinflammation by regulating microglia polarization via inhibiting NF-κB signaling

inferred← citeshttps://doi.org/10.1016/j.cclet.2022.03.003openalex-snapshot

Octacyclic and decacyclic ent‑abietane dimers with cytotoxic activity from Euphorbia fischeriana steud.

inferred← citeshttps://doi.org/10.1016/j.engmic.2022.100058openalex-snapshot

Sustainable biosynthesis of valuable diterpenes in microbes

inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105296openalex-snapshot

Structurally diverse diterpenoids from the roots of Euphorbia fischeriana Steud

inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144911openalex-snapshot

Recent advances of phenylsulfonylfuroxan derivatives and their structure-activity relationships

inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114644openalex-snapshot

Immunosuppressive spirocyclic labdane diterpenoids from Holocheila longipedunculata

inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114681openalex-snapshot

Nor-halimane and spiro-labdane diterpenoids with anti-inflammatory activity from Leucas ciliata Benth

inferred← citeshttps://doi.org/10.1016/j.synbio.2022.08.002openalex-snapshot

Norditerpenoids biosynthesized by variediene synthase-associated P450 machinery along with modifications by the host cell Aspergillus oryzae

inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152203openalex-snapshot

Saudiarabicains A-E, bioactive 19-acetoxyingol diterpenoids from Euphorbia saudiarabica

inferred← citeshttps://doi.org/10.1016/j.ymben.2024.02.006openalex-snapshot

Combinatorial biosynthesis in yeast leads to over 200 diterpenoids

inferred← citeshttps://doi.org/10.1021/acs.accounts.0c00798openalex-snapshot

Tetracyclic Diterpenoid Synthesis Facilitated by ODI-Cascade Approaches to Bicyclo[3.2.1]octane Skeletons

inferred← citeshttps://doi.org/10.1021/acs.jafc.2c08176openalex-snapshot

Antibiotic Guanacastane Diterpenoids with Two New Skeletons from Psathyrella candolleana Uncovered by Semisolid and Liquid Media

inferred← citeshttps://doi.org/10.1021/acs.jafc.3c03460openalex-snapshot

Esterification with a Long-Chain Fatty Acid Elevates the Exposure Toxicity of Tigliane Diterpenoids from Euphorbia fischeriana Roots against Nematodes

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00775openalex-snapshot

Spiroarborin, an ent-Clerodane Homodimer from Callicarpa arborea as an Inhibitor of the Eleven-Nineteen Leukemia (ENL) Protein by Targeting the YEATS Domain

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02920openalex-snapshot

Syntheses of Skeletally Diverse Tetracyclic Isodon Diterpenoid Scaffolds Guided by Dienyne Radical Cyclization Logic

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03383openalex-snapshot

Synthesis of Seven-Membered Cross-Conjugated Cyclic Trienes by 8π Electrocyclic Reaction

inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01076openalex-snapshot

Total Synthesis of the Alleged Structure of (+)-Fimbricalyxoid A

inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01924openalex-snapshot

Biochemical and Genetic Basis of Guanacastane Diterpene Biosynthesis in Basidiomycete Fungi

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00926openalex-snapshot

Unveiling the Biosynthesis of Sphaerols A–E: Catalyzed by Two Uncommon Diterpene Synthases AsSS and CvSS

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03589openalex-snapshot

Construction of the Tetracyclic Core of Isoabietenin A

inferred← citeshttps://doi.org/10.1021/acscatal.4c05274openalex-snapshot

Unexpected Main-Chain-Mediated and Neutral-Intermediate-Involved Catalytic Reaction in a High-Fidelity ent-Neoabietadiene Synthase

inferred← citeshttps://doi.org/10.1038/s41467-023-38154-9openalex-snapshot

Allylic hydroxylation of enones useful for the functionalization of relevant drugs and natural products

inferred← citeshttps://doi.org/10.1038/s41467-023-39706-9openalex-snapshot

Molecular insights into the catalytic promiscuity of a bacterial diterpene synthase

inferred← citeshttps://doi.org/10.1038/s41598-026-47487-6openalex-snapshot

Effect of nanoemulsions of Araucaria heterophylla and Azadirachta indica leaf extracts against Culex pipiens: biochemical impacts and phytochemical profile

inferred← citeshttps://doi.org/10.1039/d2np00034bopenalex-snapshot

[2 + 2]-Cycloaddition-derived cyclobutane natural products: structural diversity, sources, bioactivities, and biomimetic syntheses

inferred← citeshttps://doi.org/10.1039/d2ob00053aopenalex-snapshot

Unprecedented diterpenoid dimers with soluble epoxide hydrolase inhibitory effect from Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1080/1040841x.2021.1933898openalex-snapshot

The genus Paraconiothyrium : species concepts, biological functions, and secondary metabolites

inferred← citeshttps://doi.org/10.1080/14786419.2025.2473573openalex-snapshot

New 14,15-dinor- neo -clerodane and neo -clerodane diterpenoids from Ajuga macrosperma Wall. ex benth

inferred← citeshttps://doi.org/10.1080/14786419.2026.2662424openalex-snapshot

Specific transformation of steviol at unactivated C-H sites by microorganism and mining of key P450 enzymes

inferred← citeshttps://doi.org/10.1101/2023.03.24.534067openalex-snapshot

Production of 130 diterpenoids by combinatorial biosynthesis in yeast

inferred← citeshttps://doi.org/10.1111/pbi.13933openalex-snapshot

Structural and mechanistic insights into the precise product synthesis by a bifunctional miltiradiene synthase

inferred← citeshttps://doi.org/10.1590/s1678-9946202062097openalex-snapshot

Anti-Zika virus activity of several abietane-type ferruginol analogues

inferred← citeshttps://doi.org/10.3390/cancers12102957openalex-snapshot

An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines

inferred← citeshttps://doi.org/10.3390/fermentation10070349openalex-snapshot

Advances and Challenges in Biomanufacturing of Glycosylation of Natural Products

inferred← citeshttps://doi.org/10.3390/ijms25126691openalex-snapshot

Talaroacids A–D and Talaromarane A, Diterpenoids with Anti-Inflammatory Activities from Mangrove Endophytic Fungus Talaromyces sp. JNQQJ-4

inferred← citeshttps://doi.org/10.3390/ijms252413332openalex-snapshot

Design, Synthesis, and Biological Evaluation of Novel Urea-Containing Carnosic Acid Derivatives with Anticancer Activity

inferred← citeshttps://doi.org/10.3390/jof8030244openalex-snapshot

Diterpenes Specially Produced by Fungi: Structures, Biological Activities, and Biosynthesis (2010–2020)

inferred← citeshttps://doi.org/10.3390/molecules25102382openalex-snapshot

NMR-Based Chemical Profiling, Isolation and Evaluation of the Cytotoxic Potential of the Diterpenoid Siderol from Cultivated Sideritis euboea Heldr.

inferred← citeshttps://doi.org/10.3390/molecules27238303openalex-snapshot

A Review of Diterpenes from Marine-Derived Fungi: 2009–2021

inferred← citeshttps://doi.org/10.3390/molecules28114367openalex-snapshot

The Corey-Seebach Reagent in the 21st Century: A Review

inferred← citeshttps://doi.org/10.3390/molecules28114472openalex-snapshot

Zeylleucapenoids A–D, Highly Oxygenated Diterpenoids with Anti-Inflammatory Activity from Leucas zeylanica (L.) R. Br.

inferred← citeshttps://doi.org/10.3390/molecules31152653openalex-snapshot

A Review of Plant-Derived Diterpenoid Biosynthesis: From Structural Scaffold Diversity and Lineage-Associated Distribution to Enzyme Mining and Discovery Strategies

inferred← citeshttps://doi.org/10.3390/ph19091435openalex-snapshot

Andrographolide as a Promising Diterpenoid Scaffold Against the Neurotropic Nematode Angiostrongylus cantonensis

inferred← citeshttps://doi.org/10.59761/rcr5104openalex-snapshot

The green chemistry paradigm in modern organic synthesis

inferred← citeshttps://doi.org/10.70675/5e45bb7az93d3z4c80zbc60zed1b729bd936openalex-snapshot

Biosynthèse et rôle biologique des diterpènes dans les graines de caféiers

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