Preparation of enantiomerically pure fructose-derived 1,3-oxazin-2-one by INIR methodology and its application as a chiral auxiliary in some model asymmetric reactions-Reference-Cited by-同舟云学术

Preparation of enantiomerically pure fructose-derived 1,3-oxazin-2-one by INIR methodology and its application as a chiral auxiliary in some model asymmetric reactions

Published:1998-08 Issue:33 Volume:54 Page:9765-9784
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Banks Malcolm R.,Cadogan J.I.G.,Gosney Ian,Gould Robert O.,Hodgson Philip K.G.,McDougall Douglas

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. (5R)-7,8:9,10-Di-O-isopropylidene-2,6-dioxa-4-azaspiro[4,5]decan-3-one: a new chiral spirooxazolidin-2-one derived from D-(+)-galactose for use in asymmetric transformations

2. Highly regio- and stereo-specific preparation of a new carbohydrate-based 1,3-oxazin-2-one by the INIR method and its applications in some asymmetric transformations

3. Synthetic studies with carbohydrate-derived chiral auxiliaries

4. Carbohydrates as Chiral Auxiliaries in Stereoselective Synthesis. New Synthetic Methods(90)

5. Stereoselective syntheses using carbohydrates as chiral auxiliaries

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