An enantiospecific approach to an oxepane related to zoapatanol via a 1,3-dipolar cycloaddition

Tony Kung Ming Shing, Ching Hung Wong

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

The optically active oxepane 2, which is a suitable intermediate for a synthesis of zoapatanol 1, has been constructed from D-glucose involving an intramolecular nitrile oxide cycloaddtion as the key step.

Original languageEnglish
Pages (from-to)1151-1154
Number of pages4
JournalTetrahedron: Asymmetry
Volume5
Issue number7
DOIs
Publication statusPublished - 1994 Jan 1
Externally publishedYes

Fingerprint

Nitriles
Cycloaddition
nitriles
cycloaddition
glucose
Oxides
Glucose
oxides
synthesis
zoapatanol

ASJC Scopus subject areas

  • Catalysis
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

Cite this

An enantiospecific approach to an oxepane related to zoapatanol via a 1,3-dipolar cycloaddition. / Shing, Tony Kung Ming; Wong, Ching Hung.

In: Tetrahedron: Asymmetry, Vol. 5, No. 7, 01.01.1994, p. 1151-1154.

Research output: Contribution to journalArticle

Shing, Tony Kung Ming ; Wong, Ching Hung. / An enantiospecific approach to an oxepane related to zoapatanol via a 1,3-dipolar cycloaddition. In: Tetrahedron: Asymmetry. 1994 ; Vol. 5, No. 7. pp. 1151-1154.
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