Facile syntheses of cyclopnellitol and its (1R,6S)-, (1R,2S,6S)-, (2S)-diastereoisomers from (-)-quinic acid

Tony Kung Ming Shing, Vincent W.F. Tai

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

Cyclophellitol and its (1R,6S)-, (1R,2S,6S)-, (2S)-diastereoisomers are constructed from quinic acid involving a regioselective cyclic sulfate ring opening reaction, a regiospecific oxidative elimination, and an epoxidation reaction.

Original languageEnglish
Pages (from-to)995-997
Number of pages3
JournalJournal of the Chemical Society, Chemical Communications
Issue number12
DOIs
Publication statusPublished - 1993 Dec 1
Externally publishedYes

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Quinic Acid
Epoxidation
Sulfates
Acids
cyclophellitol

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Facile syntheses of cyclopnellitol and its (1R,6S)-, (1R,2S,6S)-, (2S)-diastereoisomers from (-)-quinic acid. / Shing, Tony Kung Ming; Tai, Vincent W.F.

In: Journal of the Chemical Society, Chemical Communications, No. 12, 01.12.1993, p. 995-997.

Research output: Contribution to journalArticle

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