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Stereoselective Synthesis and Determination of the Cytotoxic Properties of Spicigerolide and Three of Its Stereoisomers

https://doi.org/10.1021/jo034470y
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What this work says

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

inferredcites →https://doi.org/10.1016/s0040-4020(00)00987-xopenalex-snapshot
Application of molecular mechanics in the total stereochemical elucidation of spicigerolide, a cytotoxic 6-tetraacetyloxyheptenyl-5,6-dihydro-α-pyrone from Hyptis spicigera
inferredcites →https://doi.org/10.1016/s0040-4020(02)01594-6openalex-snapshot
Stereoselective synthesis of (−)-malyngolide, (+)-malyngolide and (+)-tanikolide using ring-closing metathesis
inferredcites →https://doi.org/10.1016/s0040-4020(97)00199-3openalex-snapshot
Regio- and stereoselective synthesis of γ-alkylidenebutenolides and related compounds
inferredcites →https://doi.org/10.1016/s0040-4020(99)00304-xopenalex-snapshot
Olefin metathesis by molybdenum imido alkylidene catalysts
inferredcites →https://doi.org/10.1016/s0040-4039(00)95645-4openalex-snapshot
A convergent total synthesis of (−)-anamarine from d-glucose
inferredcites →https://doi.org/10.1016/s0040-4039(00)96881-3openalex-snapshot
A convergent total synthesis of (+)-anamarine from (R,R)-tartrate and D-gulonolactone
inferredcites →https://doi.org/10.1021/ar000114fopenalex-snapshot
The Development of L 2 X 2 RuCHR Olefin Metathesis Catalysts: An Organometallic Success Story
inferredcites →https://doi.org/10.1021/jo025813fopenalex-snapshot
Stereoselective Synthesis of (+)-Boronolide
inferredcites →https://doi.org/10.1021/ol0265463openalex-snapshot
Stereoselective Synthesis of Microcarpalide

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.2021.112706zenodo-depositor-declared
Distribution of 5,6-dihydro-α-pyrones by electrospray ionization ion trap mass spectrometry in different aerial parts of Hyptis monticola
inferred← citeshttps://doi.org/10.1002/0471264180.or073.01openalex-snapshot
Allylboration of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/0471264180.or089.01openalex-snapshot
Olefin Ring‐Closing Metathesis
inferred← citeshttps://doi.org/10.1002/chem.200600335openalex-snapshot
α,β‐Unsaturated δ‐Lactones from Copper‐Catalyzed Asymmetric Vinylogous Mukaiyama Reactions of Aldehydes: Scope and Mechanistic Insights
inferred← citeshttps://doi.org/10.1002/chem.201301980openalex-snapshot
Dynamic Kinetic Resolution of Homoallylic Alcohols: Application to the Synthesis of Enantiomerically Pure 5,6‐Dihydropyran‐2‐ones and δ‐Lactones
inferred← citeshttps://doi.org/10.1002/chin.200347232openalex-snapshot
Stereoselective Synthesis and Determination of the Cytotoxic Properties of Spicigerolide and Three of Its Stereoisomers.
inferred← citeshttps://doi.org/10.1002/ejoc.200600570openalex-snapshot
Synthetic Approaches to α,β‐Unsaturated δ‐Lactones and Lactols
inferred← citeshttps://doi.org/10.1002/mrc.4178openalex-snapshot
DFT 1H–1H coupling constants in the conformational analysis and stereoisomeric differentiation of 6‐heptenyl‐2H‐pyran‐2‐ones: configurational reassignment of synargentolide A
inferred← citeshttps://doi.org/10.1007/s00894-016-3079-9openalex-snapshot
Conformational and reactivity study of dithiophenyl-fucosyl ketals with theoretical chemical methods
inferred← citeshttps://doi.org/10.1007/s43450-022-00333-yopenalex-snapshot
From Relative to Absolute Stereochemistry of Secondary Metabolites: Applications in Plant Chemistry
inferred← citeshttps://doi.org/10.1016/j.carres.2010.05.002openalex-snapshot
Acetonation of l-pentoses and 6-deoxy-l-hexoses under kinetic control using heterogeneous acid catalysts
inferred← citeshttps://doi.org/10.1016/j.ccr.2004.10.009openalex-snapshot
The chemistry of the carbon-transition metal double and triple bond: annual survey covering the year 2003
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.03.033openalex-snapshot
Transition metals in organic synthesis: Highlights for the year 2003
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2010.02.010openalex-snapshot
Synthesis of gem-difluoromethylenated analogues of anamarine
inferred← citeshttps://doi.org/10.1016/j.tet.2004.02.003openalex-snapshot
Stereoselective synthesis of anamarine
inferred← citeshttps://doi.org/10.1016/j.tet.2004.10.010openalex-snapshot
Stereoselective synthesis of hyptolide and 6-epi-hyptolide
inferred← citeshttps://doi.org/10.1016/j.tet.2006.03.073openalex-snapshot
Stereoselective synthesis of pachastrissamine (jaspine B)
inferred← citeshttps://doi.org/10.1016/j.tet.2006.12.047openalex-snapshot
Stereoselective syntheses of naturally occurring 5,6-dihydropyran-2-ones
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.10.001openalex-snapshot
An efficient synthesis of synargentolide A from d-mannitol
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.02.010openalex-snapshot
Stereoselective total synthesis of the cytotoxic lactone (−)-spicigerolide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.07.033openalex-snapshot
Total synthesis of hyptolide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.05.099openalex-snapshot
An efficient total synthesis of (−)-anamarine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.12.114openalex-snapshot
Stereoselective synthesis of pectinolide C
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00965openalex-snapshot
Hyptolactones and Their Biological Potential: A Systematic Review
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00953openalex-snapshot
Complementarity of DFT Calculations, NMR Anisotropy, and ECD for the Configurational Analysis of Brevipolides K–O from Hyptis brevipes
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00908openalex-snapshot
Structure Elucidation, Conformation, and Configuration of Cytotoxic 6-Heptyl-5,6-dihydro-2H-pyran-2-ones from Hyptis Species and Their Molecular Docking to α-Tubulin
inferred← citeshttps://doi.org/10.1021/cr400008hopenalex-snapshot
Diastereoselective Allylation of Carbonyl Compounds and Imines: Application to the Synthesis of Natural Products
inferred← citeshttps://doi.org/10.1021/jo049275dopenalex-snapshot
Stereoselective Synthesis of the Antiprotozoal Lactone Passifloricin A and Seven Isomers Thereof
inferred← citeshttps://doi.org/10.1021/jo051681popenalex-snapshot
De Novo Asymmetric Synthesis of Anamarine and Its Analogues
inferred← citeshttps://doi.org/10.1021/jo200637gopenalex-snapshot
Vicinal 1H–1H NMR Coupling Constants from Density Functional Theory as Reliable Tools for Stereochemical Analysis of Highly Flexible Multichiral Center Molecules
inferred← citeshttps://doi.org/10.1021/jo500420jopenalex-snapshot
Studies of (−)-Pironetin Binding to α-Tubulin: Conformation, Docking, and Molecular Dynamics
inferred← citeshttps://doi.org/10.1021/jo8025753openalex-snapshot
Stereoselective Synthesis of (−)-Spicigerolide
inferred← citeshttps://doi.org/10.1021/np300740hopenalex-snapshot
Absolute Configuration and Conformational Analysis of Brevipolides, Bioactive 5,6-Dihydro-α-pyrones from Hyptis brevipes
inferred← citeshttps://doi.org/10.1021/np800447kopenalex-snapshot
Structural Reassignment, Absolute Configuration, and Conformation of Hypurticin, a Highly Flexible Polyacyloxy-6-heptenyl-5,6-dihydro-2H-pyran-2-one
inferred← citeshttps://doi.org/10.1021/ol047322iopenalex-snapshot
Enantioselective Synthesis of 10-epi-Anamarine via an Iterative Dihydroxylation Sequence
inferred← citeshttps://doi.org/10.1021/ol047352lopenalex-snapshot
Asymmetric Total Synthesis of Rollicosin
inferred← citeshttps://doi.org/10.1021/ol052332kopenalex-snapshot
Total Synthesis of (+)-Phomopsolide C by Ring-Size Selective Ring-Closing Metathesis/Cross-Metathesis
inferred← citeshttps://doi.org/10.1055/a-1730-9857openalex-snapshot
Chiron Approach for the Total Synthesis of Brevipolide M
inferred← citeshttps://doi.org/10.1134/s1070363214070342openalex-snapshot
Synthesis of the 2,3,4-triacetyl-1,6-dideoxy-L-mannose and tetracetyl-3,6-dideoxy-L-mannitol and the study of the reaction mechanism by molecular modeling
inferred← citeshttps://doi.org/10.3390/molecules25081905openalex-snapshot
Recent Advances in the Stereoselective Total Synthesis of Natural Pyranones Having Long Side Chains
inferred← citeshttps://doi.org/10.3390/plants12020296openalex-snapshot
Molecular Docking of Cryptoconcatones to α-Tubulin and Related Pironetin Analogues
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