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A practical asymmetric synthesis of homochiral alpha-arylglycines

Abstract:
Enantioselective reduction of a series of substituted aryl trichloromethyl ketones with the CBS-catecholborane reagent afforded homochiral aryl trichloromethyl carbinols which have been elaborated to give homochiral α-arylglycines in high e.e. © 2001 Elsevier Science Ltd.
Publication status:
Published

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
Journal:
TETRAHEDRON-ASYMMETRY
Volume:
12
Issue:
1
Pages:
149-155
Publication date:
2001-02-05
DOI:
ISSN:
0957-4166
Source identifiers:
110601
Language:
English
Pubs id:
pubs:110601
UUID:
uuid:1c5e3ce7-5db2-4851-aa93-645eb3a2f297
Local pid:
pubs:110601
Deposit date:
2012-12-19

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