Synthesis of conagenin analogs modified at 3′-carbon atom

Three conagenin analogs modified at 3′-carbon centre and their diastereoisomers at position C-2 were synthesized. The synthesis of the acylating carboxylic acids 13, 22 and 33 having stereotriads were elaborated starting from d-xylose performing stereoselective reactions. Three conagenin analogs mod...

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Bibliographic Details
Published in:Tetrahedron 1997-10, Vol.53 (40), p.13883-13896
Main Authors: Kovács-Kulyassa, Árpád, Herczegh, Pál, Sztaricskai, Ferenc
Format: Article
Language:English
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Summary:Three conagenin analogs modified at 3′-carbon centre and their diastereoisomers at position C-2 were synthesized. The synthesis of the acylating carboxylic acids 13, 22 and 33 having stereotriads were elaborated starting from d-xylose performing stereoselective reactions. Three conagenin analogs modified at 3′-carbon centre and their diastereoisomers at position C-2 were synthesized. The synthesis of the acylating carboxylic acids 13, 22 and 33 were elaborated starting from D-xylose performing stereoselective reactions.
ISSN:0040-4020
1464-5416
DOI:10.1016/S0040-4020(97)00877-6