(-)-Quinic acid in organic synthesis. 3. Stereocontrolled syntheses of pseudo-α-d-glucopyranose and pseudo-α-d-mannopyranose.

Tony K.M. Shing; Yu xin Cui; Ying Tang

doi:10.1016/S0040-4020(01)88756-1

(-)-Quinic acid in organic synthesis. 3. Stereocontrolled syntheses of pseudo-α-d-glucopyranose and pseudo-α-d-mannopyranose.

Tony K.M. Shing, Yu xin Cui, Ying Tang

Department of Chemistry

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

33 Citations (Scopus)

Abstract

The alkene (16), readily affordable from (-)-quinic acid, underwent a stereoselective cis-and trans-hydroxylation to give pseudo-α-d-glucopyranose (1) and pseudo-α-d-mannopyranose (2) respectively.

Original language	English
Pages (from-to)	2349-2358
Number of pages	10
Journal	Tetrahedron
Volume	48
Issue number	12
DOIs	https://doi.org/10.1016/S0040-4020(01)88756-1
Publication status	Published - 1992 Mar 20

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4020(01)88756-1

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title = "(-)-Quinic acid in organic synthesis. 3. Stereocontrolled syntheses of pseudo-α-d-glucopyranose and pseudo-α-d-mannopyranose.",

abstract = "The alkene (16), readily affordable from (-)-quinic acid, underwent a stereoselective cis-and trans-hydroxylation to give pseudo-α-d-glucopyranose (1) and pseudo-α-d-mannopyranose (2) respectively.",

author = "Shing, {Tony K.M.} and Cui, {Yu xin} and Ying Tang",

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AU - Cui, Yu xin

AU - Tang, Ying

PY - 1992/3/20

Y1 - 1992/3/20

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AB - The alkene (16), readily affordable from (-)-quinic acid, underwent a stereoselective cis-and trans-hydroxylation to give pseudo-α-d-glucopyranose (1) and pseudo-α-d-mannopyranose (2) respectively.

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(-)-Quinic acid in organic synthesis. 3. Stereocontrolled syntheses of pseudo-α-d-glucopyranose and pseudo-α-d-mannopyranose.

Abstract

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