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Total synthesis of (+)-costunolide
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inferred← citeshttps://doi.org/10.1002/047084289x.rt137.pub2openalex-snapshot
p-Toluenesulfonylhydrazide
inferred← citeshttps://doi.org/10.1002/0471264180.or044.01openalex-snapshot
Preparation of α,β‐Unsaturated Carbonyl Compounds and Nitriles by Selenoxide Elimination
inferred← citeshttps://doi.org/10.1002/9780470129685.ch1openalex-snapshot
Total Synthesis of Sesquiterpenes, 1970‐79
inferred← citeshttps://doi.org/10.1002/9783527654628.ch7openalex-snapshot
Stereochemistry, Controlled or Uncontrolled?
inferred← citeshttps://doi.org/10.1002/ange.200804228openalex-snapshot
Total Synthesis of the Originally Assigned Structure of Vannusal B
inferred← citeshttps://doi.org/10.1002/anie.200804228openalex-snapshot
Total Synthesis of the Originally Assigned Structure of Vannusal B
inferred← citeshttps://doi.org/10.1002/cbdv.200900406openalex-snapshot
Secondary Metabolites of Plants from the Genus Saussurea: Chemistry and Biological Activity
inferred← citeshttps://doi.org/10.1002/cbdv.200900418openalex-snapshot
Cytotoxic Sesquiterpenes from Magnolia kachirachirai
inferred← citeshttps://doi.org/10.1002/cber.19891220910openalex-snapshot
Synthese mittlerer und großer Ringe, XXIV: Regioselektive Oxidation von 10‐Oxo‐3,6‐hexanooxepin‐4,5‐dicarbonsäure‐diethylester — ein neuer Weg zu hochfunktionalisierten Zehnringen und Hydroazulenlactonen
inferred← citeshttps://doi.org/10.1002/chin.197742348openalex-snapshot
ChemInform Abstract: TOTAL SYNTHESIS OF (+)‐COSTUNOLIDE
inferred← citeshttps://doi.org/10.1002/ejoc.202500816openalex-snapshot
Ring Formation in Sesquiterpene Synthesis: Biomimetic vs. Non‐Biomimetic Strategies
inferred← citeshttps://doi.org/10.1002/hlca.19820650407openalex-snapshot
Note on the Synthesis of 1, 1‐Dichloro‐2, 3‐divinylcyclopropane and Other Functionalized Dichlorocyclopropanes
inferred← citeshttps://doi.org/10.1002/jlac.198019800203openalex-snapshot
Synthese natürlich vorkommender p‐Hydroxyacetophenon‐Derivate, III
inferred← citeshttps://doi.org/10.1002/jlac.198119811220openalex-snapshot
Hochselektive Totalsynthese von 19‐Nor‐Steroiden mit photochemischer Schlüsselreaktion: Racemische Zielverbindungen1,4)
inferred← citeshttps://doi.org/10.1002/jlac.198819881016openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/recl.19891081104openalex-snapshot
Synthetic approaches to glutinosone
inferred← citeshttps://doi.org/10.1007/978-1-4899-3420-8_3openalex-snapshot
Terpenes (Including Steroids)
inferred← citeshttps://doi.org/10.1007/bf02975329openalex-snapshot
Synthesis of sesquiterpene derivatives as potential antitumor agents; Elemane derivatives
inferred← citeshttps://doi.org/10.1007/s00894-008-0274-3openalex-snapshot
Ab initio analysis of the Cope rearrangement of germacrane sesquiterpenoids
inferred← citeshttps://doi.org/10.1007/s12272-001-1154-0openalex-snapshot
Melanogenesis inhibitory compounds from Saussureae Radix
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Preparation of 2,3-seco-5α-cholestane-2,3-diol and 4α-methyl-2,3-seco-5α-cholestane-2,3-diol and its reactions with o-nitrophenyl selenocyanate
inferred← citeshttps://doi.org/10.1016/0040-4020(80)80024-xopenalex-snapshot
Methodology for the construction of quaternary carbon centers
inferred← citeshttps://doi.org/10.1016/0040-4020(94)00938-qopenalex-snapshot
Biotransformation of (±)-4,8-dimethylcyclodeca-3(E),7(E)- dien-1β-ol and (+)-hedycaryol by Cichorium intybus
inferred← citeshttps://doi.org/10.1016/0040-4020(95)00040-fopenalex-snapshot
Synthesis of a 1,9-dideoxy-forskolin derivative
inferred← citeshttps://doi.org/10.1016/0305-1978(91)90021-qopenalex-snapshot
Distribution of sesquiterpene lactones and polyacetylenic thiophenes in Echinops
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00251-1openalex-snapshot
Reduction of Ketones to Alkenes
inferred← citeshttps://doi.org/10.1016/b978-0-12-697252-8.50006-6openalex-snapshot
Organoselenium Oxidations
inferred← citeshttps://doi.org/10.1016/j.tet.2008.08.114openalex-snapshot
Ti-catalyzed transannular cyclization of epoxygermacrolides. Synthesis of antifungal (+)-tuberiferine and (+)-dehydrobrachylaenolide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.10.045openalex-snapshot
Enantioselective route to ferrugine and its methyl analogue via aldol deoxygenation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154102openalex-snapshot
Synthesis of (1Z)-deacylcnicin
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)80397-5openalex-snapshot
Synthesis of terpenoid compounds from α-santonin
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)85916-0openalex-snapshot
Total synthesis of various elemanolides
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)87733-4openalex-snapshot
Macroring contraction methodology
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)89119-5openalex-snapshot
Synthesis of various natural 8,12-elemanolides from artemisin
inferred← citeshttps://doi.org/10.1016/s0040-4020(03)00788-9openalex-snapshot
Synthesis of a 1α-amino-1-deoxy analogue of forskolin
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)00025-3openalex-snapshot
The synthesis of germacrane sesquiterpenes and related compounds
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)81828-6openalex-snapshot
A general synthetic method for 2,6-cyclodecadienone system by intramolecular alkylation of protected cyanohydrins
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)80972-2openalex-snapshot
Total synthesis of the germacranolide (±)-aristolactone via [2,3] wittig ring contraction
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)85882-2openalex-snapshot
An unusual reduction of a cross conjugated dienone. Stereoselective synthesis of (−)-Dictyolene
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)10775-4openalex-snapshot
Palladium II promoted rearrangement of germacranolides. Synthesis of (+)-stoebenolide and (+)-dehydromelitensin
inferred← citeshttps://doi.org/10.1016/s0079-6468(08)70009-2openalex-snapshot
6 Progress in the Medicinal Chemistry of the Herb Feverfew
inferred← citeshttps://doi.org/10.1016/s1572-5995(00)80044-7openalex-snapshot
The Synthesis of Bioactive Sesquiterpenes from Santonin
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00752openalex-snapshot
Application of Cp2TiCl-Promoted Radical Cyclization: A Unified Strategy for the Syntheses of Iridoid Monoterpenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00406openalex-snapshot
Climbing the Oxidase Phase Ladder by Using Dioxygen as the Sole Oxidant: The Case Study of Costunolide
inferred← citeshttps://doi.org/10.1021/ar00086a004openalex-snapshot
Recent applications of the Shapiro reaction
inferred← citeshttps://doi.org/10.1021/ar50133a004openalex-snapshot
Functional group manipulation using organoselenium reagents
inferred← citeshttps://doi.org/10.1021/ja077569lopenalex-snapshot
Total Synthesis of (−)-Okilactomycin
inferred← citeshttps://doi.org/10.1021/ja100740topenalex-snapshot
Total Synthesis and Structural Revision of Vannusals A and B: Synthesis of the Originally Assigned Structure of Vannusal B
inferred← citeshttps://doi.org/10.1021/ja100742bopenalex-snapshot
Total Synthesis and Structural Revision of Vannusals A and B: Synthesis of the True Structures of Vannusals A and B
inferred← citeshttps://doi.org/10.1021/ja8084669openalex-snapshot
Evolution of the Total Synthesis of (−)-Okilactomycin Exploiting a Tandem Oxy-Cope Rearrangement/Oxidation, a Petasis−Ferrier Union/Rearrangement, and Ring-Closing Metathesis
inferred← citeshttps://doi.org/10.1021/jacs.8b10522openalex-snapshot
Enantioselective Conversion of Oligoprenol Derivatives to Macrocycles in the Germacrene, Cembrene, and 18-Membered Cyclic Sesterterpene Series
inferred← citeshttps://doi.org/10.1021/jm950747dopenalex-snapshot
Synthesis and Biological Activity of Novel Nonsteroidal Progesterone Receptor Antagonists Based on Cyclocymopol Monomethyl Ether
inferred← citeshttps://doi.org/10.1021/jo0256538openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/ja.2017.132openalex-snapshot
Synthesis of deoxyelephantopin analogues
inferred← citeshttps://doi.org/10.1039/a605081fopenalex-snapshot
Synthesis and NMR studies of key intermediates to a new class of β-lactam: the trinems
inferred← citeshttps://doi.org/10.1039/b602937jopenalex-snapshot
Rapid stereocontrolled assembly of the fully substituted C-aryl glycoside of kendomycin with a Prins cyclization: a formal synthesis
inferred← citeshttps://doi.org/10.1039/c8ob00033fopenalex-snapshot
Bis(phenylsulfonyl)methane mediated synthesis of olefins via a halogen elimination and double bond migration
inferred← citeshttps://doi.org/10.1039/c9np00049fopenalex-snapshot
Advances in chemistry and bioactivity of parthenolide
inferred← citeshttps://doi.org/10.1039/c9sc01473jopenalex-snapshot
Stereoselective total synthesis of parthenolides indicates target selectivity for tubulin carboxypeptidase activity
inferred← citeshttps://doi.org/10.1055/s-0040-1720348openalex-snapshot
Efficient Construction of (±)-epi-Costunolide through a Chromium(II)-Mediated Nozaki–Hiyama–Kishi Reaction
inferred← citeshttps://doi.org/10.1080/00397918408060733openalex-snapshot
A Mild Method for the Formation of Tosylhydrazone Derivatives from Keto Esters
inferred← citeshttps://doi.org/10.1080/00397919908086464openalex-snapshot
Synthesis of Substituted γ-Butyrolactones: β-Hydroxymethyl-, β-Methylene and Cyclopropane Derivatives
inferred← citeshttps://doi.org/10.1104/pp.010957openalex-snapshot
Biosynthesis of Costunolide, Dihydrocostunolide, and Leucodin. Demonstration of Cytochrome P450-Catalyzed Formation of the Lactone Ring Present in Sesquiterpene Lactones of Chicory
inferred← citeshttps://doi.org/10.1246/bcsj.58.146openalex-snapshot
Synthetic Studies on Germacranolides. Synthesis of Optically Active 3-Oxygenated 13-Norheliangolides
inferred← citeshttps://doi.org/10.1246/cl.1978.617openalex-snapshot
STUDIES ON THE SYNTHESES OF SESQUITERPENE LACTONES IV. TOTAL SYNTHESIS OF SAUSSUREA LACTONE
inferred← citeshttps://doi.org/10.1246/cl.1982.249openalex-snapshot
SYNTHESIS OF 3-OXYGENATED 13-NORHELIANG0LIDES
inferred← citeshttps://doi.org/10.1246/cl.1986.85openalex-snapshot
SYNTHESIS OF (±)-COSTUNOLIDE, AN ANTITUMOR GERMACRANOLIDE, FROM E,E-FARNESOL BY USE OF A LOW-VALENT CHROMIUM REAGENT
inferred← citeshttps://doi.org/10.31390/gradschool_disstheses.3895openalex-snapshot
New Sesquiterpene Lactones From the Genera Calea and Berlandiera (Asteraceae) and the Fragmentation Reactions of 1,3-Dihydroxyeudesmanolide Derivatives.
inferred← citeshttps://doi.org/10.3390/ijms22031052openalex-snapshot
Natural and Synthetic Lactones Possessing Antitumor Activities
inferred← citeshttps://doi.org/10.3390/molecules27062023openalex-snapshot
Structure-Based Molecular Networking for the Discovery of Anti-HBV Compounds from Saussurea lappa (Decne.) C.B Clarke
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