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Ring-fused gem-dibromocyclopropanes as precursors to enantiomerically pure D- and L-series 3-deoxy- and 2-amino-2,3-dideoxyaldohexose derivatives

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Date

2001

Authors

Banwell, Martin
Ebenbeck, Wolfgang
Edwards, Alison

Journal Title

Journal ISSN

Volume Title

Publisher

Royal Society of Chemistry

Abstract

The gem-dibromocyclopropanes that undergo silver(1)-promoted electrocyclic ring-opening and the resulting π-allyl cations trapped with a range of nucleophiles to give mixtures of cyclohexenyl bromides were discussed. It was found that the subjection of t

Description

Keywords

Keywords: Aromatic hydrocarbons; Derivatives; Desulfurization; Mixtures; Positive ions; Reduction; Enantiomers; Carbohydrates

Citation

URI

http://hdl.handle.net/1885/94174

Collections

ANU Research Publications

Source

Journal of the Chemical Society, Perkin Transactions 1

Type

Journal article

Book Title

Entity type

Access Statement

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DOI

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