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Volumn 131, Issue 13, 2009, Pages 4904-4916

Total synthesis of vinblastine, vincristine, related natural products, and key structural analogues

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL EVALUATION; CATHARANTHINE; COUPLING EFFICIENCY; COUPLING REACTION; DIASTEREO-SELECTIVITY; DIASTEREOSELECTIVE; DIRECT COUPLING; DOUBLE BONDS; FORMYL GROUP; FUNCTIONALIZED; IMINIUM; METHOXY GROUP; METHYL GROUP; NATURAL PRODUCTS; NATURALLY OCCURRING; OXIDATION REACTIONS; OXIDATIVE FRAGMENTATION; OXIDIZED CARBONS; RADICAL CATIONS; REACTION MIXTURE; STRUCTURAL ANALOGUE; TOTAL SYNTHESIS; VINBLASTINE; VINDOLINE;

EID: 67949110944     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja809842b     Document Type: Article
Times cited : (307)

References (100)
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    • The single-crystal X-ray structure of 28 establishing its structure and relative stereochemistry was derived from off-white crystals obtained from EtOAc and has been deposited with the Cambridge Crystallographic Data Centre (CCDC 713670).
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    • The substrates 33 and 34 were prepared utilizing the tandem [4 + 2]/[3 + 2] 1,3,4-oxadiazole cycloaddition cascade as detailed in the Supporting Information with a chromatographic resolution.
    • The substrates 33 and 34 were prepared utilizing the tandem [4 + 2]/[3 + 2] 1,3,4-oxadiazole cycloaddition cascade as detailed in the Supporting Information with a chromatographic resolution.


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