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

Tony K.M. Shing; Ching Hung Wong

doi:10.1016/0957-4166(94)80143-6

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

Tony K.M. Shing, Ching Hung Wong

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

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 language	English
Pages (from-to)	1151-1154
Number of pages	4
Journal	Tetrahedron: Asymmetry
Volume	5
Issue number	7
DOIs	https://doi.org/10.1016/0957-4166(94)80143-6
Publication status	Published - 1994 Jul

ASJC Scopus subject areas

Catalysis
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry

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10.1016/0957-4166(94)80143-6

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

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.",

author = "Shing, {Tony K.M.} and Wong, {Ching Hung}",

year = "1994",

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AU - Wong, Ching Hung

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IS - 7

ER -

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

Abstract

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