Synthesis of conagenin analogs modified at 3'-carbon atom

DOI: 10.1016/S0040-4020(97)00877-6

Source and publish data:

Tetrahedron p. 13883 - 13896 (1997)

Update date:2022-08-05

Topics:

Authors:

Kovacs-Kulyassa, Arpad

Herczegh, Pal

Sztaricskai, Ferenc

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Article abstract of DOI:10.1016/S0040-4020(97)00877-6

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

Full text of DOI:10.1016/S0040-4020(97)00877-6

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