The conversion of glucose into an early zincophorin synthon

Jozua F. Booysen; Cedric W. Holzapfel

doi:10.1080/00397919508011759

The conversion of glucose into an early zincophorin synthon

Jozua F. Booysen, Cedric W. Holzapfel

Chemical Sciences

University of Johannesburg

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

19 Citations (Scopus)

Abstract

The consecutive stereoselective introduction of carbon nucleophiles at the 4- and 1-positions of a suitable pseudoglycal is shown to be an efficient route to the chiral 1,4-disubstituted tetrahydropyran (2), an early zincophorin synthon.

Original language	English
Pages (from-to)	1473-1488
Number of pages	16
Journal	Synthetic Communications
Volume	25
Issue number	10
DOIs	https://doi.org/10.1080/00397919508011759
Publication status	Published - 1 May 1995

ASJC Scopus subject areas

Organic Chemistry

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title = "The conversion of glucose into an early zincophorin synthon",

abstract = "The consecutive stereoselective introduction of carbon nucleophiles at the 4- and 1-positions of a suitable pseudoglycal is shown to be an efficient route to the chiral 1,4-disubstituted tetrahydropyran (2), an early zincophorin synthon.",

author = "Booysen, {Jozua F.} and Holzapfel, {Cedric W.}",

year = "1995",

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N2 - The consecutive stereoselective introduction of carbon nucleophiles at the 4- and 1-positions of a suitable pseudoglycal is shown to be an efficient route to the chiral 1,4-disubstituted tetrahydropyran (2), an early zincophorin synthon.

AB - The consecutive stereoselective introduction of carbon nucleophiles at the 4- and 1-positions of a suitable pseudoglycal is shown to be an efficient route to the chiral 1,4-disubstituted tetrahydropyran (2), an early zincophorin synthon.

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DO - 10.1080/00397919508011759

M3 - Article

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SP - 1473

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JO - Synthetic Communications

JF - Synthetic Communications

IS - 10

ER -

The conversion of glucose into an early zincophorin synthon

Abstract

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