Synthesis of conagenin analogs modified at 3'-carbon atom

Árpád Kovács-Kulyassa, P. Herczegh, F. Sztaricskai

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)13883-13896
Number of pages14
JournalTetrahedron
Volume53
Issue number40
DOIs
Publication statusPublished - Oct 6 1997

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Starlings
Xylose
Carboxylic Acids
Carbon
Atoms
conagenin

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Synthesis of conagenin analogs modified at 3'-carbon atom. / Kovács-Kulyassa, Árpád; Herczegh, P.; Sztaricskai, F.

In: Tetrahedron, Vol. 53, No. 40, 06.10.1997, p. 13883-13896.

Research output: Contribution to journalArticle

Kovács-Kulyassa, Árpád ; Herczegh, P. ; Sztaricskai, F. / Synthesis of conagenin analogs modified at 3'-carbon atom. In: Tetrahedron. 1997 ; Vol. 53, No. 40. pp. 13883-13896.
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