Stereochemical control in the formation of thiazolidines from O-protected reducing sugars

DOI: 10.1016/0008-6215(94)84011-3

Source and publish data:

Carbohydrate Research p. 147 - 154 (1994)

Update date:2022-08-04

Topics:

Authors:

Wadouchi

Beaupere

Uzan Uzan

Stasik Stasik

Ewing Ewing

Mackenzie

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Article abstract of DOI:10.1016/0008-6215(94)84011-3

A synthetic procedure for the formation of thiazolidines from O-protected reducing sugars is described. The procedure allows access to five variations in the pattern of the protecting groups in the thiazolidine derived from D-mannose whilst maintaining co

Full text of DOI:10.1016/0008-6215(94)84011-3

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