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Tigliane Diterpenoids from the Euphorbiaceae and Thymelaeaceae Families

https://doi.org/10.1021/cr200397n

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Diterpenes from European Euphorbia Species Serving as Prototypes for Natural‐Product‐Based Drug Discovery

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EUPHORBIOID INFLORESCENCES FROM THE MIDDLE EOCENE CLAIBORNE FORMATION

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Über Inhaltsstoffe von Euphorbiaceae, VI. Drei neue 4‐Desoxyphorboltriester aus Euphovbia biglandulosa Desf.

inferredcites →https://doi.org/10.1002/lipi.19710730404openalex-snapshot

Tumorpromovierende Diterpen‐Fettsäureester aus Euphorbia triangularis und Euphorbia cooperi

inferredcites →https://doi.org/10.1002/mrc.1260250420openalex-snapshot

13C NMR spectroscopy of phorbol esters

inferredcites →https://doi.org/10.1002/ptr.2650070220openalex-snapshot

Oligo‐ and macrocyclic diterpenes in thymelaeaceae and euphorbiaceae occurring and utilized in yunnan (Southwest China) 4. Tigliane type diterpene esters (phorbol–12,13‐diesters) from Wikstroemia canescens

inferredcites →https://doi.org/10.1002/ptr.2650080209openalex-snapshot

Oligo‐ and macrocyclic diterpenes in thymelaeaceae and Euphorbiaceae occurring and utilized in Yunnan (Southwest China). 6. Tigliane type diterpene esters from latex of Euphorbia prolifera

inferredcites →https://doi.org/10.1002/ptr.2650090704openalex-snapshot

Medicinal plants of euphorbiaceae occurring and utilized in thailand. V. Skin irritants of the daphnane and tigliane type in latex of Excoecaria bicolor and the uterotonic activity of the leaves of the tree

inferredcites →https://doi.org/10.1007/bf00284369openalex-snapshot

�ber die Wirkstoffe der Euphorbiaceen

inferredcites →https://doi.org/10.1007/bf00305019openalex-snapshot

�ber die Wirkstoffe der Euphorbiaceen

inferredcites →https://doi.org/10.1007/bf00390980openalex-snapshot

On the active principles of the spurge family (Euphorbiaceae)

inferredcites →https://doi.org/10.1007/bf00988202openalex-snapshot

Effects of diterpene esters of tigliane, daphnane, ingenane, and lathyrane types on pink bollworm,Pectinophora gossypiella saunders (Lepidoptera: Gelechiidae)

inferredcites →https://doi.org/10.1007/bf01919683openalex-snapshot

Diterpene esters from ‘Euphorbium’ and their irritant and cocarcinogenic activity

inferredcites →https://doi.org/10.1007/bf01922325openalex-snapshot

Candletoxins A and B, 2 new aromatic esters of 12-deoxy-16-hydroxy-phorbol, from the irritant latex of Euphorbia poisonii Pax

inferredcites →https://doi.org/10.1007/bf01933991openalex-snapshot

New tigliane and daphnane derivatives fromPimelea prostrata andPimelea simplex

inferredcites →https://doi.org/10.1007/bf01967918openalex-snapshot

Sapintoxin A, a new biologically active nitrogen containing phorbol ester

inferredcites →https://doi.org/10.1007/bf02636256openalex-snapshot

Short‐chain phorbol ester constituents of croton oil

inferredcites →https://doi.org/10.1007/bf02854894openalex-snapshot

Drug discovery from natural sources

inferredcites →https://doi.org/10.1007/bf02859039openalex-snapshot

The Euphorbiales: Chemistry, Taxonomy and Economic Botany

inferredcites →https://doi.org/10.1007/s004320000214openalex-snapshot

Dietary cancer risk from conditional cancerogens (tumor promoters) in produce of livestock fed on species of spurge ( Euphorbiaceae )

inferredcites →https://doi.org/10.1016/0031-9422(75)85119-3openalex-snapshot

New diterpene esters from Aleurites fordii fruits

inferredcites →https://doi.org/10.1016/0031-9422(75)85388-xopenalex-snapshot

New diesters of 12-deoxy-phorbol

inferredcites →https://doi.org/10.1016/0031-9422(76)85110-2openalex-snapshot

Proteinbiosynthesen in dormanten und nachgereiften embryonen und samen von Agrostemma githago

inferredcites →https://doi.org/10.1016/0031-9422(77)80075-7openalex-snapshot

A new phorbol triester from the latices of Euphorbia frankiana and E. Coerulescens

inferredcites →https://doi.org/10.1016/0031-9422(81)85279-xopenalex-snapshot

Nitrogen-containing phorbol derivatives of Sapium indicum

inferredcites →https://doi.org/10.1016/0031-9422(83)80228-3openalex-snapshot

Phorbol derivatives from Sapium insigne

inferredcites →https://doi.org/10.1016/0031-9422(84)83091-5openalex-snapshot

Irritant phorbol derivatives from four Jatropha species

inferredcites →https://doi.org/10.1016/0031-9422(88)80615-0openalex-snapshot

Diterpenes from the latex of Euphorbia broteri

inferredcites →https://doi.org/10.1016/0040-4039(94)02455-kopenalex-snapshot

Stereocontrolled syntheses of phorbol analogs and evaluation of their binding affinity to PKC

inferredcites →https://doi.org/10.1016/0040-4039(95)01864-eopenalex-snapshot

Photoaffinity labeling of PKC with a phorbol derivative: Importance of the 13-acyl group in phorbol ester-PKC interaction

inferredcites →https://doi.org/10.1016/0041-0101(78)90060-0openalex-snapshot

The irritant toxins of Blue Euphorbia (Euphorbia coerulescens Haw.)

inferredcites →https://doi.org/10.1016/0041-0101(87)90141-3openalex-snapshot

Toxic phorbol esters from Chinese tallow stimulate protein kinase C

inferredcites →https://doi.org/10.1016/0042-6822(90)90237-lopenalex-snapshot

The phorbol ester TPA strongly inhibits HIV-1-induced syncytia formation but enhances virus production: Possible involvement of protein kinase C pathway

inferredcites →https://doi.org/10.1016/j.bcp.2007.12.004openalex-snapshot

Differential effects of phorbol-13-monoesters on human immunodeficiency virus reactivation

inferredcites →https://doi.org/10.1016/j.bmc.2005.04.056openalex-snapshot

Synthesis of new phorbol derivatives having ethereal side chain and evaluation of their anti-HIV activity

inferredcites →https://doi.org/10.1016/j.bmcl.2012.01.057openalex-snapshot

Tigliane diterpene esters with IFN γ-inducing activity from the leaves of Aleurites fordii

inferredcites →https://doi.org/10.1016/j.drudis.2007.10.010openalex-snapshot

Plant-derived compounds in clinical trials

inferredcites →https://doi.org/10.1016/j.ejmech.2007.03.016openalex-snapshot

Anti-tumor 12-deoxyphorbol esters from Euphorbia cornigera

inferredcites →https://doi.org/10.1016/j.fitote.2012.01.001openalex-snapshot

Isolation, stability and bioactivity of Jatropha curcas phorbol esters

inferredcites →https://doi.org/10.1016/j.phytochem.2007.01.017openalex-snapshot

Diterpenoids and triterpenoids from Euphorbia guyoniana

inferredcites →https://doi.org/10.1016/j.tet.2009.03.014openalex-snapshot

Isolation and structure determination of new 4,12-dideoxyphorbol esters from Euphorbia pannonica Host.

inferredcites →https://doi.org/10.1016/s0021-9258(17)44245-1openalex-snapshot

Protein kinase C as a possible receptor protein of tumor-promoting phorbol esters.

inferredcites →https://doi.org/10.1016/s0021-9673(00)90154-7openalex-snapshot

Isolation and purification of phorbol from croton oil by reversed-phase column chromatography

inferredcites →https://doi.org/10.1016/s0024-3205(96)00567-xopenalex-snapshot

Euphorbium: Modern research on its active principle, resiniferatoxin, revives an ancient medicine

inferredcites →https://doi.org/10.1016/s0031-9422(00)84408-8openalex-snapshot

A new cryptic irritant and cocarcinogen from seeds of Croton sparciflorus

inferredcites →https://doi.org/10.1016/s0031-9422(00)89024-xopenalex-snapshot

Two new toxins from the latex of Euphorbia poisonii

inferredcites →https://doi.org/10.1016/s0031-9422(00)94608-9openalex-snapshot

Two minor diterpenes from Euphorbia latex

inferredcites →https://doi.org/10.1016/s0031-9422(00)95276-2openalex-snapshot

Sapatoxins, aliphatic ester tigliane diterpenes from Sapium indicum

inferredcites →https://doi.org/10.1016/s0031-9422(00)97483-1openalex-snapshot

a new aromatic ester diterpene from Euphorbia poisonii

inferredcites →https://doi.org/10.1016/s0031-9422(96)00605-xopenalex-snapshot

Diterpenoids from Euphorbia fischeriana

inferredcites →https://doi.org/10.1016/s0031-9422(97)00786-3openalex-snapshot

Diterpenes and sterols from Neoboutonia melleri

inferredcites →https://doi.org/10.1016/s0031-9422(99)00166-1openalex-snapshot

Jatrophane and tigliane diterpenes from the latex of Euphorbia obtusifolia

inferredcites →https://doi.org/10.1016/s0031-9422(99)00556-7openalex-snapshot

Anti-HIV-1 phorbol esters from the seeds of Croton tiglium

inferredcites →https://doi.org/10.1016/s0040-4039(00)72207-6openalex-snapshot

Resiniferatoxin and other esters of novel polyfuncticnal diterpenes from Euphorbia resinifera and unispina

inferredcites →https://doi.org/10.1016/s0040-4039(00)78635-7openalex-snapshot

New irritant diterpene-esters from roots of L. (Euphorbiaceae)

inferredcites →https://doi.org/10.1016/s0040-4039(00)79841-8openalex-snapshot

Oxidation of aldehydes to acyl azides by chromic anhydride-azidotrimethylsilane

inferredcites →https://doi.org/10.1016/s0040-4039(00)90549-5openalex-snapshot

The synthesis of functionally substituted optically active derivatives of imino-2, 5-dihydrofurans.

inferredcites →https://doi.org/10.1016/s0040-4039(00)92940-xopenalex-snapshot

The structure of prostratin : a toxic tetracyclic diterpene ester from Pimelea Prostrata

inferredcites →https://doi.org/10.1016/s0040-4039(01)81895-5openalex-snapshot

4-deoxyphorbol and 4α-deoxyphorbol aldehydes new diterpenes and their esters

inferredcites →https://doi.org/10.1016/s0040-4039(01)88434-3openalex-snapshot

Tumor promoting compounds from euphorbia triangularis: mono- and diesters of 12-desoxy-phorbol

inferredcites →https://doi.org/10.1016/s0040-4039(01)89890-7openalex-snapshot

Structure and stereochemistry of the tetracyclic diterpene phorbol from croton tiglium L.

inferredcites →https://doi.org/10.1016/s0040-4039(01)92793-5openalex-snapshot

The new diterpene 4-deoxyphorbol and its highly unsaturated irritant diesters

inferredcites →https://doi.org/10.1016/s0040-4039(01)97771-8openalex-snapshot

Tumor-promoting compounds from euphorbia cooperi di- and triesters of 16-hydroxy-12-desoxy-phorbol.

inferredcites →https://doi.org/10.1016/s0166-3542(03)00034-2openalex-snapshot

Activation of latent HIV-1 expression by the potent anti-tumor promoter 12-deoxyphorbol 13-phenylacetate

inferredcites →https://doi.org/10.1016/s0166-3542(96)01004-2openalex-snapshot

Antireplicative and anticytopathic activities of prostratin, a non-tumor-promoting phorbol ester, against human immunodeficiency virus (HIV)1

inferredcites →https://doi.org/10.1016/s0367-326x(00)00314-2openalex-snapshot

A new phorbol diester from Aleurites moluccana

inferredcites →https://doi.org/10.1016/s0378-8741(03)00010-2openalex-snapshot

Tigliane diterpenes from the latex of Euphorbia obtusifolia with inhibitory activity on the mammalian mitochondrial respiratory chain

inferredcites →https://doi.org/10.1016/s0960-894x(01)00045-2openalex-snapshot

The C4 hydroxyl group of phorbol esters is not necessary for protein kinase C binding

inferredcites →https://doi.org/10.1021/cr0782832openalex-snapshot

Plant Orthoesters

inferredcites →https://doi.org/10.1021/cr078350sopenalex-snapshot

Chemical and Pharmacological Research of the Plants in Genus Euphorbia

inferredcites →https://doi.org/10.1021/ja00168a050openalex-snapshot

Studies on tumor promoters. 9. A second-generation synthesis of phorbol

inferredcites →https://doi.org/10.1021/ja00206a050openalex-snapshot

Studies on tumor promoters. 8. The synthesis of phorbol

inferredcites →https://doi.org/10.1021/ja00248a042openalex-snapshot

Studies on tumor promoters: the first synthesis of the phorbol skeleton

inferredcites →https://doi.org/10.1021/ja010643uopenalex-snapshot

Formal Synthesis of (+)-Phorbol 1

inferredcites →https://doi.org/10.1021/ja027048sopenalex-snapshot

Dramatic Switching of Protein Kinase C Agonist/Antagonist Activity by Modifying the 12-Ester Side Chain of Phorbol Esters

inferredcites →https://doi.org/10.1021/ja9706256openalex-snapshot

The First Formal Asymmetric Synthesis of Phorbol

inferredcites →https://doi.org/10.1021/jm00089a006openalex-snapshot

A nonpromoting phorbol from the Samoan medicinal plant Homalanthus nutans inhibits cell killing by HIV-1

inferredcites →https://doi.org/10.1021/jm9001007openalex-snapshot

Modulation of the Transient Receptor Potential Vanilloid Channel TRPV4 by 4α-Phorbol Esters: A Structure−Activity Study

inferredcites →https://doi.org/10.1021/jm950509iopenalex-snapshot

Selectively Cytotoxic Diterpenes from Euphorbia poisonii

inferredcites →https://doi.org/10.1021/np020060dopenalex-snapshot

Novel 12-Deoxy-16-hydroxyphorbol Diesters Isolated from the Seed Oil of Jatropha curcas

inferredcites →https://doi.org/10.1021/np020115bopenalex-snapshot

Isolation and Structure of Pedilstatin from a Republic of Maldives Pedilanthus sp.

inferredcites →https://doi.org/10.1021/np0204489openalex-snapshot

Antimycobacterial Activity of Phorbol Esters from the Fruits of Sapium indicum

inferredcites →https://doi.org/10.1021/np030096lopenalex-snapshot

Natural Products as Sources of New Drugs over the Period 1981−2002

inferredcites →https://doi.org/10.1021/np040106yopenalex-snapshot

The Role of Natural Product Chemistry in Drug Discovery

inferredcites →https://doi.org/10.1021/np0600088openalex-snapshot

Diterpenoids from the Roots of Euphorbia fischeriana

inferredcites →https://doi.org/10.1021/np0604174openalex-snapshot

Tigliane Diterpenoids from the Stem Bark of Neoboutonia macrocalyx

inferredcites →https://doi.org/10.1021/np068054vopenalex-snapshot

Natural Products as Sources of New Drugs over the Last 25 Years

inferredcites →https://doi.org/10.1021/np1005746openalex-snapshot

Daphnane- and Tigliane-Type Diterpenoid Esters and Orthoesters from Pimelea elongata

inferredcites →https://doi.org/10.1021/np100673sopenalex-snapshot

Unusual Tigliane Diterpenes from Euphorbia grandicornis

inferredcites →https://doi.org/10.1021/np200058copenalex-snapshot

Tigliane-Type Diterpenoid Glycosides from Euphorbia fischeriana

inferredcites →https://doi.org/10.1021/np200241copenalex-snapshot

Isolation and Biological Evaluation of Jatrophane Diterpenoids from Euphorbia dendroides

inferredcites →https://doi.org/10.1021/np300637topenalex-snapshot

Prostratin and 12-O-Tetradecanoylphorbol 13-Acetate Are Potent and Selective Inhibitors of Chikungunya Virus Replication

inferredcites →https://doi.org/10.1021/np300815topenalex-snapshot

Isolation, Structure Determination, and Anti-HIV Evaluation of Tigliane-Type Diterpenes and Biflavonoid from Stellera chamaejasme

inferredcites →https://doi.org/10.1021/np300832nopenalex-snapshot

Cytotoxic Phorbol Esters of Croton tiglium

inferredcites →https://doi.org/10.1021/np50018a021openalex-snapshot

Sapintoxin D, A New Phorbol Ester From Sapium indicum

inferredcites →https://doi.org/10.1021/np50025a013openalex-snapshot

Plant Anticancer Agents. XXII. Isolation of a Phorbol Diester and Its Δ5,6-7β-Hydroperoxide Derivative From Ostodes paniculata

inferredcites →https://doi.org/10.1021/np50041a021openalex-snapshot

Unambiguous 1H-nmr Assignment of Phorbol Triacetate Using a Two-Dimensional NMR Technique

inferredcites →https://doi.org/10.1021/np50045a002openalex-snapshot

On the Active Principles of the Euphorbiaceae, XII. Highly Unsaturated Irritant Diterpene Esters from Euphorbia tirucalli Originating from Madagascar

inferredcites →https://doi.org/10.1021/np50060a003openalex-snapshot

Irritant Principles of the Spurge Family (Euphorbiaceae) XIII. Oligocyclic and Macrocyclic Diterpene Esters from Latices of Some Euphorbia Species Utilized as Source Plants of Honey

inferredcites →https://doi.org/10.1021/np50075a011openalex-snapshot

Antitumor Agents, 119. Kansuiphorins A and B, Two Novel Antileukemic Diterpene Esters from Euphorbia kansui

inferredcites →https://doi.org/10.1021/np50119a020openalex-snapshot

A Novel Phorbol Ester from Excoecaria agallocha

inferredcites →https://doi.org/10.1021/np800295mopenalex-snapshot

Variability in Content of the Anti-AIDS Drug Candidate Prostratin in Samoan Populations of Homalanthus nutans

inferredcites →https://doi.org/10.1021/np9005053openalex-snapshot

Terpenoids from Daphne aurantiaca and Their Potential Anti-inflammatory Activity

inferredcites →https://doi.org/10.1021/np9604893openalex-snapshot

Natural Products in Drug Discovery and Development

inferredcites →https://doi.org/10.1021/np990209uopenalex-snapshot

Diterpenoids from Euphorbia pithyusa subsp. cupanii

inferredcites →https://doi.org/10.1039/c39890000183openalex-snapshot

Isolation and structure determination of a novel phorbol derivative in an intramolecular diester macrolide

inferredcites →https://doi.org/10.1055/s-0028-1097367openalex-snapshot

Potential Anticancer Agents VIII.

inferredcites →https://doi.org/10.1055/s-0028-1099610openalex-snapshot

ZUM WIRKUNGSMECHANISMUS COCARCINOGENER PFLANZENINHALTSSTOFFE

inferredcites →https://doi.org/10.1055/s-2005-873196openalex-snapshot

New Macrocyclic Lathyrane Diterpenes, fromEuphorbia lagascae,as Inhibitors of Multidrug Resistance of Tumour Cells

inferredcites →https://doi.org/10.1055/s-2006-959499openalex-snapshot

Cryptic and Free Skin Irritants of the Daphnane and Tigliane Types in Latex ofExcoecaria agallocha1

inferredcites →https://doi.org/10.1055/s-2006-962001openalex-snapshot

An Antitumor Principle fromEuphorbia lathyris

inferredcites →https://doi.org/10.1055/s-2006-962531openalex-snapshot

Tigliane-Type Diterpene Esters fromSynadenium grantii1,5

inferredcites →https://doi.org/10.1055/s-2007-969623openalex-snapshot

Structure Activity Relations of Polyfunctional Diterpenes of the Tigliane Type, VI1

inferredcites →https://doi.org/10.1055/s-2007-969798openalex-snapshot

Active Principles of the Thymelaeaceae

inferredcites →https://doi.org/10.1055/s-2007-969850openalex-snapshot

Skin Irritant and Tumor Promoting Diterpene Esters of the Tigliane Type from the Chinese Tallow Tree (Sapium sebiferum)*

inferredcites →https://doi.org/10.1055/s-2007-971250openalex-snapshot

On the Active Principles of the Thymelaeaceae

inferredcites →https://doi.org/10.1055/s-2007-971369openalex-snapshot

On the Active Principles of the Thymelaeaceae

inferredcites →https://doi.org/10.1055/s-2007-993765openalex-snapshot

Three New Jatrophane Polyesters and Antiproliferative Constituents from Euphorbia tuckeyana

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The Constituents of Australian Pimelea spp. I. The Isolation and Structure of the Toxin of Pimelea simplex and P. trichostachya Form B Responsible for St. George Disease of Cattle

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Phorbol diester receptor copurifies with protein kinase C.

inferredcites →https://doi.org/10.1074/jbc.m402124200openalex-snapshot

Prostratin Antagonizes HIV Latency by Activating NF-κB

inferredcites →https://doi.org/10.1080/10286020.2010.532490openalex-snapshot

Diterpenoids from the roots ofEuphorbia fischeriana

inferredcites →https://doi.org/10.1080/10286020.2012.757596openalex-snapshot

Two new diterpenoids fromExcoecaria acerifolia

inferredcites →https://doi.org/10.1080/10286020.2013.786703openalex-snapshot

Two new tigliane diterpene esters from the flower buds ofDaphne genkwa

inferredcites →https://doi.org/10.1080/10915810701464641openalex-snapshot

Phorbol Esters: Structure, Biological Activity, and Toxicity in Animals

inferredcites →https://doi.org/10.1093/oxfordjournals.bmb.a072822openalex-snapshot

COCARCINOGENESIS

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A chemotaxonomic survey of flavonoids and simple phenols in leaves of the Ericaceae

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Structure/Activity Relationships of Polyfunctional Diterpenes of the Tigliane Type

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Some Naturrally Occurring Skin Irritants

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The Succulent Euphorbias of Nigeria. III. Structure and Potency of the Aromatic Ester Diterpenes of Euphorbia Poissonii Pax

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New Phorbol and Deoxyphorbol Esters: Isolation and Relative Potencies in Inducing Platelet Aggregation and Erythema of Skin

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PHORBOL ESTER RECEPTORS AND THE IN VITRO EFFECTS OF TUMOR PROMOTERS

inferredcites →https://doi.org/10.1111/j.2042-7158.1975.tb09450.xopenalex-snapshot

Skin irritants of Euphorbia fortissima

inferredcites →https://doi.org/10.1111/j.2042-7158.1985.tb14095.xopenalex-snapshot

Activation of Protein Kinase C By Tumour-Promoting and Non-Promoting Phorbol Esters

inferredcites →https://doi.org/10.1126/science.1154690openalex-snapshot

Practical Synthesis of Prostratin, DPP, and Their Analogs, Adjuvant Leads Against Latent HIV

inferredcites →https://doi.org/10.1126/science.1251193openalex-snapshot

Antileukemic Principles Isolated from Euphorbiaceae Plants

inferredcites →https://doi.org/10.1128/jvi.76.16.8118-8123.2002openalex-snapshot

Effects of Prostratin on T-Cell Activation and Human Immunodeficiency Virus Latency

inferredcites →https://doi.org/10.1139/v79-331openalex-snapshot

Carbon-13 nuclear magnetic resonance spectroscopy of phorbol

inferredcites →https://doi.org/10.1152/physrev.00021.2006openalex-snapshot

Transient Receptor Potential Cation Channels in Disease

inferredcites →https://doi.org/10.1177/095632020401500404openalex-snapshot

Mechanisms of HIV Receptor and Co-Receptor Down-Regulation by Prostratin: Role of Conventional and Novel PKC Isoforms

inferredcites →https://doi.org/10.1177/135965350400900415openalex-snapshot

Prostratin Induces HIV Activation and Downregulates HIV Receptors in Peripheral Blood Lymphocytes

inferredcites →https://doi.org/10.1182/blood.v98.10.3006openalex-snapshot

Prostratin: activation of latent HIV-1 expression suggests a potential inductive adjuvant therapy for HAART

inferredcites →https://doi.org/10.1248/cpb.22.971openalex-snapshot

The Toxic Constituent of the Fruits of Aleurites fordii

inferredcites →https://doi.org/10.1248/cpb.50.523openalex-snapshot

Inhibition of Cytopathic Effect of Human Immunodeficiency Virus Type-1 by Various Phorbol Derivatives.

inferredcites →https://doi.org/10.1248/cpb.57.1289openalex-snapshot

Diterpene Esters and Phenolic Compounds from Sapium insigne (ROYLE) BENTH. ex HOOK. fil.

inferredcites →https://doi.org/10.1515/znb-1977-0632openalex-snapshot

Notizen: 4α-Sapinine — a Novel Diterpene Ester from Sapium Indicum

inferredcites →https://doi.org/10.1590/s0102-695x2012005000050openalex-snapshot

Anti-ulcer activity of Synadenium grantii latex

inferredcites →https://doi.org/10.3390/metabo2020303openalex-snapshot

A Historical Overview of Natural Products in Drug Discovery

inferredcites →https://doi.org/10.3724/sp.j.1009.2010.00264openalex-snapshot

Chemical Constituents from the Roots of Vernicia fordii

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.2020.112519zenodo-depositor-declared

Bond reactivity indices approach analysis of the [2+2] cycloaddition of jatrophane skeleton diterpenoids from Euphorbia gaditana Coss to tetracyclic gaditanone

inferred← citeshttps://doi.org/10.2139/ssrn.4678397openalex-extracted

Gas and Tar Species Evolved During Rapid Pyrolysis of California Chaparral

inferred← citeshttps://doi.org/10.2139/ssrn.4724888openalex-extracted

Gas and Tar Species Evolved During Rapid Pyrolysis of California Chaparral

inferred← citeshttps://doi.org/10.1002/ange.201509160openalex-snapshot

Total Synthesis of Crotophorbolone

inferred← citeshttps://doi.org/10.1002/ange.201706845openalex-snapshot

Total Syntheses of the Reported Structures of Curcusones I and J through Tandem Gold Catalysis

inferred← citeshttps://doi.org/10.1002/ange.201805578openalex-snapshot

Enantioselective Synthesis of Chiral Cyclopent‐2‐enones by Nickel‐Catalyzed Desymmetrization of Malonate Esters

inferred← citeshttps://doi.org/10.1002/ange.201915876openalex-snapshot

Total Synthesis of (−)‐Pepluanol B: Conformational Control of the Eight‐Membered‐Ring System

inferred← citeshttps://doi.org/10.1002/ange.202218025openalex-snapshot

Site‐ and Stereoselective C(sp3)−H Borylation of Strained (Hetero)Cycloalkanols Enabled by Iridium Catalysis

inferred← citeshttps://doi.org/10.1002/ange.202400943openalex-snapshot

Total Synthesis of the Euphorbia Diterpenoid Pepluacetal

inferred← citeshttps://doi.org/10.1002/ange.202409997openalex-snapshot

Asymmetric Total Synthesis of Euphordraculoate A and Pedrolide

inferred← citeshttps://doi.org/10.1002/ange.202423746openalex-snapshot

Chalcogen Bonding Catalysis Enables Ring‐Opening of Cyclopropene and Ring Expansion of Aryl Ketones

inferred← citeshttps://doi.org/10.1002/anie.201509160openalex-snapshot

Total Synthesis of Crotophorbolone

inferred← citeshttps://doi.org/10.1002/anie.201706845openalex-snapshot

Total Syntheses of the Reported Structures of Curcusones I and J through Tandem Gold Catalysis

inferred← citeshttps://doi.org/10.1002/anie.201805578openalex-snapshot

Enantioselective Synthesis of Chiral Cyclopent‐2‐enones by Nickel‐Catalyzed Desymmetrization of Malonate Esters

inferred← citeshttps://doi.org/10.1002/anie.201915876openalex-snapshot

Total Synthesis of (−)‐Pepluanol B: Conformational Control of the Eight‐Membered‐Ring System

inferred← citeshttps://doi.org/10.1002/anie.202218025openalex-snapshot

Site‐ and Stereoselective C(sp3)−H Borylation of Strained (Hetero)Cycloalkanols Enabled by Iridium Catalysis

inferred← citeshttps://doi.org/10.1002/anie.202400943openalex-snapshot

Total Synthesis of the Euphorbia Diterpenoid Pepluacetal

inferred← citeshttps://doi.org/10.1002/anie.202409997openalex-snapshot

Asymmetric Total Synthesis of Euphordraculoate A and Pedrolide

inferred← citeshttps://doi.org/10.1002/anie.202423746openalex-snapshot

Chalcogen Bonding Catalysis Enables Ring‐Opening of Cyclopropene and Ring Expansion of Aryl Ketones

inferred← citeshttps://doi.org/10.1002/ardp.70080openalex-snapshot

New Anti‐HIV Agents Isolated From Two Euphorbia Species

inferred← citeshttps://doi.org/10.1002/asia.202200896openalex-snapshot

Total Synthesis of Natural Products using Gold Catalysis

inferred← citeshttps://doi.org/10.1002/asia.202400184openalex-snapshot

COAP‐Pd Catalyzed Asymmetric Formal [3+2] Cycloaddition for Optically Active Multistereogenic Spiro Cyclopentane‐Indandiones Bearing Cyclic N‐Sulfonyl Ketimine Skeletons

inferred← citeshttps://doi.org/10.1002/cctc.202400947openalex-snapshot

Enantioselective Desymmetrization of 1,3‐Dicarbonyl Compounds through Transition‐Metal‐Catalyzed Intramolecular Cyclization Reactions

inferred← citeshttps://doi.org/10.1002/chem.201804904openalex-snapshot

New Casbanes and the First trans‐Cyclopropane seco‐Casbane from the Australian Rainforest Plant Croton insularis

inferred← citeshttps://doi.org/10.1002/chem.201901687openalex-snapshot

Continued Progress towards Efficient Functionalization of Natural and Non‐natural Targets under Mild Conditions: Oxygenation by C−H Bond Activation with Dioxirane

inferred← citeshttps://doi.org/10.1002/chem.202003221openalex-snapshot

Synthetic Tigliane Intermediates Engage Thiols to Induce Potent Cell Line Selective Anti‐Cancer Activity

inferred← citeshttps://doi.org/10.1002/chem.202003741openalex-snapshot

The Total Synthesis of Diquinane‐Containing Natural Products

inferred← citeshttps://doi.org/10.1002/cjoc.202100565openalex-snapshot

Chiral Pool Guided Syntheses of Polycyclic Natural Products

inferred← citeshttps://doi.org/10.1002/cjoc.202400085openalex-snapshot

Synthetic Studies toward Pseudolaric Acids: Radical Cyclization to Form Bridged Scaffold

inferred← citeshttps://doi.org/10.1002/cjoc.202400898openalex-snapshot

Total Syntheses of Highly Oxidized Natural Products†

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

Recent progress and new perspectives for diterpenoid biosynthesis in medicinal plants

inferred← citeshttps://doi.org/10.1002/slct.202002836openalex-snapshot

Diterpenoids: Natural Distribution, Semisynthesis at Room Temperature and Pharmacological Aspects‐A Decade Update

inferred← citeshttps://doi.org/10.1002/slct.202100206openalex-snapshot

Applications of Yamaguchi Method to Esterification and Macrolactonization in Total Synthesis of Bioactive Natural Products

inferred← citeshttps://doi.org/10.1007/978-3-031-67180-7_1openalex-snapshot

Tigliane Diterpenoids

inferred← citeshttps://doi.org/10.1007/978-3-032-09901-3_1openalex-snapshot

The Diels–Alder Reaction as a Key Step in Natural Product Synthesis

inferred← citeshttps://doi.org/10.1007/978-3-032-25993-6_2openalex-snapshot

Physicochemical, Pharmacological and Molecular Aspects of Phenol and Croton Oil

inferred← citeshttps://doi.org/10.1007/978-3-319-31421-1_219-1openalex-snapshot

Microbial Production of Isoprenoids

inferred← citeshttps://doi.org/10.1007/978-3-319-31421-1_219-2openalex-snapshot

Microbial Production of Isoprenoids

inferred← citeshttps://doi.org/10.1007/978-3-319-33172-0_1openalex-snapshot

Ingenane Diterpenoids

inferred← citeshttps://doi.org/10.1007/978-3-319-50436-0_219openalex-snapshot

Microbial Production of Isoprenoids

inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_1openalex-snapshot

Introduction

inferred← citeshttps://doi.org/10.1007/s00217-025-04719-9openalex-snapshot

Physicochemical properties of protein-rich whole and defatted edible Jatropha curcas as a climate-resilient food ingredient

inferred← citeshttps://doi.org/10.1007/s10600-024-04298-3openalex-snapshot

Phorbol Derivatives of Croton Oil

inferred← citeshttps://doi.org/10.1007/s11030-021-10195-6openalex-snapshot

Cross-coupling reactions towards the synthesis of natural products

inferred← citeshttps://doi.org/10.1007/s11418-016-0987-zopenalex-snapshot

Euphorins A–H: bioactive diterpenoids from Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1007/s11418-023-01713-xopenalex-snapshot

Tigliane and daphnane diterpenoids from Thymelaeaceae family: chemistry, biological activity, and potential in drug discovery

inferred← citeshttps://doi.org/10.1007/s13361-019-02269-5openalex-snapshot

Molecularly Imprinted Polymer-Coated Probe Electrospray Ionization Mass Spectrometry Determines Phorbol Esters and Deoxyphorbol Metabolites in Jatropha curcas Leaves

inferred← citeshttps://doi.org/10.1007/s43450-024-00576-xopenalex-snapshot

Insights into the Composition of Breu Canauaru, an Enigmatic Medicinal “Resin” from Amazonia

inferred← citeshttps://doi.org/10.1016/b978-0-443-18611-0.00007-3openalex-snapshot

Casbene-derived diterpenoids

inferred← citeshttps://doi.org/10.1016/j.arabjc.2022.103807openalex-snapshot

Six new tigliane diterpenoids with anti-inflammatory activity from Euphorbia kansuensis

inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.06.025openalex-snapshot

Cytotoxic macrocyclic diterpenoids from Jatropha multifida

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108961openalex-snapshot

Tigliane glycosides from Euphorbia tirucalli as multidrug resistance modulators

inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.09.002openalex-snapshot

Antitubercular and cytotoxic tigliane-type diterpenoids from Croton tiglium

inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.128319openalex-snapshot

New phorbol ester derivatives as potent anti-HIV agents

inferred← citeshttps://doi.org/10.1016/j.cclet.2024.109955openalex-snapshot

Highly anticipated natural diterpenoids as an important source of new drugs in 2013–2023

inferred← citeshttps://doi.org/10.1016/j.cclet.2026.113232openalex-snapshot

Eufischeramines A and B: Ingenane-type diterpenoid alkaloids from Euphorbia fischeriana with potent anti-pulmonary fibrosis activity

inferred← citeshttps://doi.org/10.1016/j.chempr.2018.10.002openalex-snapshot

Total Synthesis of (±)-Prostratin

inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.118458openalex-snapshot

Exploring novel aromatase cytochrome P450-binding ligands: Molecular docking and QSAR study of phorbol esters as aromatase inhibitors

inferred← citeshttps://doi.org/10.1016/j.fitote.2015.06.021openalex-snapshot

LC-MS2-Based dereplication of Euphorbia extracts with anti-Chikungunya virus activity

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.03.009openalex-snapshot

LC-MS guided isolation of diterpenoids from Sapium insigne with α-glucosidase inhibitory activities

inferred← citeshttps://doi.org/10.1016/j.fitote.2019.02.028openalex-snapshot

Triterpenoids from Euphorbia pulcherrima with inhibitory effects on osteoclastogenesis

inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105350openalex-snapshot

Antimicrobial diterpenoids from the leaves and twigs of Croton kongensis Gagnepain.

inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107177openalex-snapshot

Tigliane and daphnane diterpenoid glucosides from the roots of Euphorbia fischeriana: isolation, structural elucidation, and anti-inflammatory activity

inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107188openalex-snapshot

Undescribed phenanthrene derivatives and tigliane-type diterpenoids from the roots and stems of Baliospermum yui

inferred← citeshttps://doi.org/10.1016/j.gresc.2026.05.006openalex-snapshot

Recent advances in the total synthesis of highly strained tetracyclic diterpenoids from Euphorbiaceae: Pepluanols and Euphorikanin A

inferred← citeshttps://doi.org/10.1016/j.jics.2021.100253openalex-snapshot

Phytochemical investigation of Euphorbia trigona

inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.09.003openalex-snapshot

Bioactive diterpenoids from Croton laevigatus

inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.10.012openalex-snapshot

Highly oxygenated and structurally diverse diterpenoids from Euphorbia helioscopia

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112360openalex-snapshot

Anti-HIV tigliane diterpenoids from Reutealis trisperma

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112523openalex-snapshot

Diterpenoids from the aerial parts of Euphorbia antiquorum and their efficacy on nitric oxide inhibition

inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114035openalex-snapshot

Structurally diverse deformed phenanthrenes from Strophioblachia fimbricalyx with cytotoxic activities by inducing cell apoptosis

inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114194openalex-snapshot

Structurally diverse diterpenoids and phenanthrene derivatives from the roots of Baliospermum solanifolium

inferred← citeshttps://doi.org/10.1016/j.phytol.2019.08.003openalex-snapshot

Metabolites from Excoecaria cochinchinensis Lour.

inferred← citeshttps://doi.org/10.1016/j.phytol.2023.03.011openalex-snapshot

Euphpepluone S, a new lathyrane diterpenoid with anti-inflammatory activity from Euphorbia peplus L.

inferred← citeshttps://doi.org/10.1016/j.phytol.2023.08.003openalex-snapshot

Tigliane diterpenoids with cytotoxic activities from Croton damayeshu

inferred← citeshttps://doi.org/10.1016/j.tet.2015.10.070openalex-snapshot

Cytotoxic tigliane-type diterpenoids from Croton tiglium

inferred← citeshttps://doi.org/10.1016/j.tet.2016.11.005openalex-snapshot

Gold catalysis-facilitated rapid synthesis of the daphnane/tigliane tricyclic core

inferred← citeshttps://doi.org/10.1016/j.tet.2019.03.036openalex-snapshot

Accessing the decarboxylative allylation–divinylcyclopropane-cycloheptadiene rearrangement from the ketone/aldehyde substrate pool

inferred← citeshttps://doi.org/10.1016/j.tet.2019.04.058openalex-snapshot

Synthetic approaches to the daphnane and tigliane diterpenes from aromatic precursors

inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.04.021openalex-snapshot

DDQ-promoted C(sp3) H phosphorylation of cycloheptatriene

inferred← citeshttps://doi.org/10.1016/j.toxicon.2020.07.023openalex-snapshot

A review on Pimelea poisoning of livestock

inferred← citeshttps://doi.org/10.1016/j.ymben.2017.12.007openalex-snapshot

High-titer production of lathyrane diterpenoids from sugar by engineered Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1016/s1875-5364(24)60587-xopenalex-snapshot

Synthesis and anti-HIV activities of phorbol derivatives

inferred← citeshttps://doi.org/10.1016/s1875-5364(24)60630-8openalex-snapshot

Seco-cyclic phorbol derivatives and their anti-HIV-1 activities

inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00760openalex-snapshot

Photochemical Approaches to Complex Chemotypes: Applications in Natural Product Synthesis

inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00834openalex-snapshot

Navigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products

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.0c00700openalex-snapshot

Anti-HIV Tigliane Diterpenoids from Wikstroemia scytophylla

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00570openalex-snapshot

LC-MS Identification, Isolation, and Structural Elucidation of Anti-HIV Tigliane Diterpenoids from Wikstroemia lamatsoensis

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c01195openalex-snapshot

Anti-HIV Tigliane-Type Diterpenoids from the Aerial Parts of Wikstroemia lichiangensis

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00752openalex-snapshot

Tigliane-Type Diterpene Esters from the Fruits of Shirakiopsis indica and Their Anti-HIV Activity

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00364openalex-snapshot

Rapid Access to Tigliane, Ingenane, and Rhamnofolane Diterpenes from a Lathyrane Precursor via Biomimetic Skeleton Transformation Strategy

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00603openalex-snapshot

Isolation of Phorbol Esters fromEuphorbia grandicornisand Evaluation of Protein Kinase C- and Human Platelet-Activating Effects of Euphorbiaceae Diterpenes

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00168openalex-snapshot

Mining Cytochrome P450 Enzymes Involved in Casbene Oxidation from Euphorbia fischeriana Steud. and Clarifying Their Substrate Specificity

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00607openalex-snapshot

Phorbol Rearrangements

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00800openalex-snapshot

Antiviral Compounds from Codiaeum peltatum Targeted by a Multi-informative Molecular Networks Approach

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00042openalex-snapshot

Cytotoxic Tigliane Diterpenoids from Croton damayeshu

inferred← citeshttps://doi.org/10.1021/acs.joc.0c00022openalex-snapshot

Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol

inferred← citeshttps://doi.org/10.1021/acs.joc.2c01024openalex-snapshot

Crotonianoids A–C, Three Unusual Tigliane Diterpenoids from the Seeds of Croton tiglium and Their Anti-Prostate Cancer Activity

inferred← citeshttps://doi.org/10.1021/acs.joc.2c01783openalex-snapshot

Acid-Promoted Iso-Nazarov Cyclization of Conjugated trans-Dienones and Dienals for the Synthesis of 2-Cyclopentenones

inferred← citeshttps://doi.org/10.1021/acs.joc.2c02247openalex-snapshot

Dual Proton/Silver-Catalyzed Serial (5 + 2)-Cycloaddition and Nazarov Cyclization of (E)-2-Arylidene-3-hydroxyindanones with Conjugated Eneynes: Synthesis of Indanone-Fused Benzo[cd]azulenes

inferred← citeshttps://doi.org/10.1021/acs.joc.3c01356openalex-snapshot

Cp2TiCl-Promoted Endo-Trig Radical Cyclization to Six- and Seven-Membered Carbocycles: Synthesis of (±)-Isoclavukerin A

inferred← citeshttps://doi.org/10.1021/acs.oprd.4c00041openalex-snapshot

Total Synthesis with Gram-Scale Radical Process: An Inspiration for Pharmaceutical Industry

inferred← citeshttps://doi.org/10.1021/acs.organomet.4c00432openalex-snapshot

Silver(I)-Catalyzed Stereochemical Isomerization of Cyclopropanols

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03647openalex-snapshot

Pedrolane, a Polycyclic Diterpene Scaffold Containing a Bicyclo[2.2.1]heptane System, from Euphorbia pedroi

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.2c03172openalex-snapshot

Ir-Catalyzed Biomimetic Photoisomerization of Cyclopropane in Lathyrane-Type Euphorbia Diterpenes

inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03109openalex-snapshot

Rearrangement of the Tetra- and Tricyclic Skeletons of Pepluanol B to Access the Core Structures of Tigliane- and Myrsinane-Type Euphorbia Diterpenes

inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03136openalex-snapshot

Asymmetric Construction of the Core of C6, C7-Epoxy Daphnane Diterpenoid Orthoesters

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01363openalex-snapshot

Conversion of Phorbol into Des-D-Ring Tricycle and Crotonianoid B via Peroxidation Reaction

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01497openalex-snapshot

A Photoinduced Radical Cascade Cyclization for the Synthesis of Angularly Fused Tricyclic Compounds

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03606openalex-snapshot

Asymmetric Construction of the Tricyclic Core Structure of Prostratin

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03473openalex-snapshot

One-Step Semisynthesis of a Segetane Diterpenoid from a Jatrophane Precursor via a Diels–Alder Reaction

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03210openalex-snapshot

Büchner Ring Expansion/Isomerization: Photoactivation of Imide-Annulated N-Heterocyclic Carbenes Affords Vicinal Diamino Cycloheptatrienes

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01093openalex-snapshot

Euphorikanin A, a Diterpenoid Lactone with a Fused 5/6/7/3 Ring System from Euphorbia kansui

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03142openalex-snapshot

Euphomilones A and B, ent-Rosane Diterpenoids with 7/5/6 and 5/7/6 Skeletons from Euphorbia milii

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02537openalex-snapshot

Regioselective and Enantioselective Intermolecular Buchner Ring Expansions in Flow

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01215openalex-snapshot

Heliojatrones A and B, Two Jatrophane-Derived Diterpenoids with a 5/10 Fused-Ring Skeleton from Euphorbia helioscopia: Structural Elucidation and Biomimetic Conversion

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03229openalex-snapshot

Iodine-Catalyzed Iso-Nazarov Cyclization of Conjugated Dienals for the Synthesis of 2-Cyclopentenones

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03379openalex-snapshot

En Route to D-Ring Inverted Phorbol Esters

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03539openalex-snapshot

Daphneodorins A–C, Anti-HIV Gnidimacrin Related Macrocyclic Daphnane Orthoesters from Daphne odora

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04484openalex-snapshot

Crokonoids A–C, A Highly Rearranged and Dual-Bridged Spiro Diterpenoid and Two Other Diterpenoids from Croton kongensis

inferred← citeshttps://doi.org/10.1021/acscatal.0c02053openalex-snapshot

Pd-Catalyzed Synthesis of Densely Functionalized Cyclopropyl Vinyl Sulfides Reveals the Origin of High Selectivity in a Fundamental Alkyne Insertion Step

inferred← citeshttps://doi.org/10.1021/acscentsci.7b00475openalex-snapshot

REDOR NMR Reveals Multiple Conformers for a Protein Kinase C Ligand in a Membrane Environment

inferred← citeshttps://doi.org/10.1021/acsmedchemlett.9b00554openalex-snapshot

Missing Selectivity of Targeted 4β-Phorbol Prodrugs Expected to be Potential Chemotherapeutics

inferred← citeshttps://doi.org/10.1021/acsomega.5c09251openalex-snapshot

Multiapproach Analysis Combined with Chemometrics for the Authentication of Commercial Oils of Croton tiglium (L.)

inferred← citeshttps://doi.org/10.1021/jacs.0c10682openalex-snapshot

Asymmetric Intramolecular Dearomatization of Nonactivated Arenes with Ynamides for Rapid Assembly of Fused Ring System under Silver Catalysis

inferred← citeshttps://doi.org/10.1021/jacs.1c00557openalex-snapshot

Total Synthesis and Target Identification of the Curcusone Diterpenes

inferred← citeshttps://doi.org/10.1021/jacs.1c06450openalex-snapshot

Unified Total Syntheses of Rhamnofolane, Tigliane, and Daphnane Diterpenoids

inferred← citeshttps://doi.org/10.1021/jacs.2c02360openalex-snapshot

Ti-Catalyzed Diastereoselective Cyclopropanation of Carboxylic Derivatives with Terminal Olefins

inferred← citeshttps://doi.org/10.1021/jacs.2c08200openalex-snapshot

Total Synthesis of Resiniferatoxin

inferred← citeshttps://doi.org/10.1021/jacs.3c02113openalex-snapshot

Enantioselective Total Synthesis of (+)-Pedrolide

inferred← citeshttps://doi.org/10.1021/jacs.3c14150openalex-snapshot

Asymmetric Total Synthesis of Pedrolide

inferred← citeshttps://doi.org/10.1021/jacs.4c01589openalex-snapshot

Total Syntheses of Phorbol and 11 Tigliane Diterpenoids and Their Evaluation as HIV Latency-Reversing Agents

inferred← citeshttps://doi.org/10.1021/jacs.5c16410openalex-snapshot

Total Synthesis of (+)-Resiniferatoxin via a Pyridinium Salt Photorearrangement

inferred← citeshttps://doi.org/10.1021/jacs.5c22127openalex-snapshot

Evolution of a Synthetic Strategy for Complex Diterpenes from Euphorbiaceae and Thymelaeaceae

inferred← citeshttps://doi.org/10.1021/jacs.6b13155openalex-snapshot

Fe-Catalyzed C–C Bond Construction from Olefins via Radicals

inferred← citeshttps://doi.org/10.1021/jacs.6c00187openalex-snapshot

Total Synthesis of (±)- and (+)-Euphohyrisnoid A

inferred← citeshttps://doi.org/10.1021/jacs.6c02838openalex-snapshot

Total Synthesis of Euphopia B and Discovery of a Selective Inhibitor of Potassium Efflux-Independent NLRP3 Inflammasome Activation

inferred← citeshttps://doi.org/10.1021/jacs.6c13015openalex-snapshot

Total Synthesis and Structural Confirmation of Curcusone I

inferred← citeshttps://doi.org/10.1021/jacs.6c13616openalex-snapshot

Divergent Syntheses of Euphorbia Diterpenoids: A Relay Rearrangement Strategy Triggered by Pyridinium Ring Contraction

inferred← citeshttps://doi.org/10.1038/nature17153openalex-snapshot

Nineteen-step total synthesis of (+)-phorbol

inferred← citeshttps://doi.org/10.1038/s41467-024-46523-1openalex-snapshot

Valence-isomer selective cycloaddition reaction of cycloheptatrienes-norcaradienes

inferred← citeshttps://doi.org/10.1038/s41557-022-01048-2openalex-snapshot

Practical synthesis of the therapeutic leads tigilanol tiglate and its analogues

inferred← citeshttps://doi.org/10.1038/s41568-020-00310-4openalex-snapshot

Equivocal, explicit and emergent actions of PKC isoforms in cancer

inferred← citeshttps://doi.org/10.1038/s41598-017-14637-wopenalex-snapshot

Two novel diterpenoid heterodimers, Bisebracteolasins A and B, from Euphorbia ebracteolata Hayata, and the cancer chemotherapeutic potential of Bisebracteolasin A

inferred← citeshttps://doi.org/10.1038/s41598-020-80397-9openalex-snapshot

Activation of PKC supports the anticancer activity of tigilanol tiglate and related epoxytiglianes

inferred← citeshttps://doi.org/10.1039/c7ob02916kopenalex-snapshot

Structural revision of two unusual rhamnofolane diterpenes, curcusones I and J, by means of DFT calculations of NMR shifts and coupling constants

inferred← citeshttps://doi.org/10.1039/c7ra08877aopenalex-snapshot

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

inferred← citeshttps://doi.org/10.1039/c8cs00532jopenalex-snapshot

Application of (4+3) cycloaddition strategies in the synthesis of natural products

inferred← citeshttps://doi.org/10.1039/c8ob02519copenalex-snapshot

Crotonols A and B, two rare tigliane diterpenoid derivatives against K562 cells from Croton tiglium

inferred← citeshttps://doi.org/10.1039/c9cc06241fopenalex-snapshot

Divergent gold-catalysed reactions of cyclopropenylmethyl sulfonamides with tethered heteroaromatics

inferred← citeshttps://doi.org/10.1039/c9cc06889aopenalex-snapshot

Highly stereoselective intramolecular Buchner reaction of diazoacetamides catalyzed by a Ru( ii )–Pheox complex

inferred← citeshttps://doi.org/10.1039/c9cc08830jopenalex-snapshot

Concise gram-scale synthesis of Euphorikanin A skeleton through a domino ring-closing metathesis strategy

inferred← citeshttps://doi.org/10.1039/c9ob02197copenalex-snapshot

Developments in the construction of cyclopropanols

inferred← citeshttps://doi.org/10.1039/d0np00042fopenalex-snapshot

Natural products in agarwood and Aquilaria plants: chemistry, biological activities and biosynthesis

inferred← citeshttps://doi.org/10.1039/d0np00086hopenalex-snapshot

Balancing skeleton and functional groups in total syntheses of complex natural products: a case study of tigliane, daphnane and ingenane diterpenoids

inferred← citeshttps://doi.org/10.1039/d0qo00424copenalex-snapshot

Facile synthesis of the daphnane and tigliane framework by semi-flow tube-based-bubbling photooxidation and diastereoselective conjugate addition

inferred← citeshttps://doi.org/10.1039/d0qo00522copenalex-snapshot

Brønsted-acid-catalyzed one-pot tandem annulation/[5 + 2]-cycloaddition of o -propargyl alcohol benzaldehydes with alkynes: regioselective and stereoselective synthesis of dibenzo[ a , f ]azulen-12-ones

inferred← citeshttps://doi.org/10.1039/d0sc02829kopenalex-snapshot

Total synthesis of crotophorbolone

inferred← citeshttps://doi.org/10.1039/d1np00065aopenalex-snapshot

Biosynthesis of cyclopropane in natural products

inferred← citeshttps://doi.org/10.1039/d1qo01312bopenalex-snapshot

Catalytic radical cascade cyclization of alkene-tethered enones to fused bicyclic cyclopropanols

inferred← citeshttps://doi.org/10.1039/d2np00047dopenalex-snapshot

Euphorbia diterpenoids: isolation, structure, bioactivity, biosynthesis, and synthesis (2013–2021)

inferred← citeshttps://doi.org/10.1039/d2ra01315kopenalex-snapshot

Highly efficient construction of an oxa-[3.2.1]octane-embedded 5–7–6 tricyclic carbon skeleton and ring-opening of the bridged ring via C–O bond cleavage

inferred← citeshttps://doi.org/10.1039/d3cc02213gopenalex-snapshot

Aminative annulation of cyano-enynyl esters leading to functionalized cyclopentenones

inferred← citeshttps://doi.org/10.1039/d3ra05058kopenalex-snapshot

Mukaiyama aldol reaction: an effective asymmetric approach to access chiral natural products and their derivatives/analogues

inferred← citeshttps://doi.org/10.1039/d3sc00119aopenalex-snapshot

Cobalt-catalyzed enantioselective desymmetrizing reductive cyclization of alkynyl cyclodiketones

inferred← citeshttps://doi.org/10.1039/d4ob01743aopenalex-snapshot

Forging the tricyclic core framework of euphordraculoate B via a Barbier-type allyl addition

inferred← citeshttps://doi.org/10.1039/d4qo02316aopenalex-snapshot

Total synthesis of cyclopropane-containing natural products: recent progress (2016–2024)

inferred← citeshttps://doi.org/10.1039/d4sc02487gopenalex-snapshot

Enantioselective phosphine-catalyzed [6 + 1] annulations of α-allyl allenoates with 1,1-bisnucleophiles

inferred← citeshttps://doi.org/10.1039/d5ob01393copenalex-snapshot

Overview of harziane diterpenoids: discovery, bioactivity, total synthesis and biosynthesis

inferred← citeshttps://doi.org/10.1039/d6ob01082bopenalex-snapshot

Mild acid-catalyzed pinacol rearrangement of phorbol derivatives: a mechanistic and synthetic study

inferred← citeshttps://doi.org/10.1055/s-0037-1611709openalex-snapshot

Asymmetric Kulinkovich Hydroxycyclopropanation of Alkenes Mediated by Titanium(IV) TADDOLate Complexes

inferred← citeshttps://doi.org/10.1055/s-0043-110227openalex-snapshot

Isolation and Structure Characterization of Cytotoxic Phorbol Esters from the Seeds of Croton tiglium

inferred← citeshttps://doi.org/10.1073/pnas.1919408117openalex-snapshot

Prodrugs of PKC modulators show enhanced HIV latency reversal and an expanded therapeutic window

inferred← citeshttps://doi.org/10.1080/10286020.2023.2197224openalex-snapshot

New abietane and tigliane diterpenoids from the roots of Euphorbia fischeriana and their cytotoxic activities

inferred← citeshttps://doi.org/10.1080/14786419.2015.1129334openalex-snapshot

A new tigliane-type diterpene from Euphorbia dracunculoides Lam

inferred← citeshttps://doi.org/10.1080/14786419.2016.1222385openalex-snapshot

A new ent-kaurane diterpene from Euphorbia stracheyi Boiss

inferred← citeshttps://doi.org/10.1080/14786419.2019.1607331openalex-snapshot

A new highly oxygenated abietane diterpenoid and a new lysosome generating phorbol ester from the roots of Euphorbia fischeriana Steud

inferred← citeshttps://doi.org/10.1080/14786419.2019.1616728openalex-snapshot

Bioactive tigliane diterpenoids from the latex of Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1080/14786419.2021.1924712openalex-snapshot

Cytotoxic tigliane diterpenoids from Euphorbia neorubella

inferred← citeshttps://doi.org/10.1080/14786419.2021.1938039openalex-snapshot

A new tigliane-type diterpenoid from Euphorbia tirucalli

inferred← citeshttps://doi.org/10.1080/14786419.2022.2147168openalex-snapshot

Tigliane-and daphnane-type diterpenoids from the buds of Daphne genkwa with their cytotoxic activities

inferred← citeshttps://doi.org/10.1093/hr/uhaf097openalex-snapshot

Genome-wide terpene gene clusters analysis in Euphorbiaceae

inferred← citeshttps://doi.org/10.1097/hm9.0000000000000004openalex-snapshot

Natural products against HIV latency

inferred← citeshttps://doi.org/10.1134/s1990793120010145openalex-snapshot

Antioxidant Properties of the Phorbol: A DFT Approach

inferred← citeshttps://doi.org/10.1177/1934578x1501001206openalex-snapshot

Macrocyclic Diterpenoids from the Latex of Euphorbia helioscopia

inferred← citeshttps://doi.org/10.1186/s13071-019-3537-1openalex-snapshot

An appraisal of natural products active against parasitic nematodes of animals

inferred← citeshttps://doi.org/10.1246/bcsj.20160208openalex-snapshot

Asymmetric Total Synthesis of Crotophorbolone: Construction of the 5/7/6-Fused Ring System via an α-Alkoxy Bridgehead Radical Reaction

inferred← citeshttps://doi.org/10.1515/psr-2021-0094openalex-snapshot

Synthesis of bioactive natural products and their analogs at room temperature – an update

inferred← citeshttps://doi.org/10.21203/rs.3.rs-3354072/v1openalex-snapshot

Valence-isomer selective cycloaddition reaction to synthesize functionalized carbocycles

inferred← citeshttps://doi.org/10.21203/rs.3.rs-6519295/v1openalex-snapshot

G-Quadruplex Folding Enforces HIV-1 Transcriptional Latency via Nucleolin Recruitment

inferred← citeshttps://doi.org/10.3389/fevo.2023.1197194openalex-snapshot

First insights into herbivore–plant interaction of the spurge hawkmoth and Euphorbia cyparissias

inferred← citeshttps://doi.org/10.3389/fpls.2022.1087899openalex-snapshot

Stereoselective (4 + 3) cycloadditions of allenyl ethers-furans by chiral auxiliaries inducing and evaluation of anti-breast cancer activity

inferred← citeshttps://doi.org/10.3389/fpls.2026.1833614openalex-snapshot

Diterpenoids in medicinal plants: structure, distribution, biological activities, biosynthesis, and bioengineering prospects

inferred← citeshttps://doi.org/10.3390/biomedicines12051021openalex-snapshot

Naturally Occurring Norsteroids and Their Design and Pharmaceutical Application

inferred← citeshttps://doi.org/10.3390/biomedicines9101353openalex-snapshot

Targeting Drug Chemo-Resistance in Cancer Using Natural Products

inferred← citeshttps://doi.org/10.3390/ijms17030398openalex-snapshot

Antiallergic Phorbol Ester from the Seeds of Aquilaria malaccensis

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