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Unexpected Cyclization During the Mitsunobu Reaction of d-Talose Derivatives

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Publication date
26 November 2014
Publisher
Doi

    Abstract

    A d-talose derivative underwent unexpected cyclization during a Mitsunobu reaction. A plausible pathway for the reaction involves an attack of the nucleophilic azide on the benzyl ring by intramolecular cyclization with loss of the benzyl group. These newly formed, unexpected compounds may be used in the synthesis of ­derivatives of C-nucleosides

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    National Chung Hsing University Institutional Repository

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    Last time updated on 16/06/2016

    This paper was published in National Chung Hsing University Institutional Repository.

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