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Asymmetric synthesis of aldol products derived from unsymmetrical ketones: assignment of the absolute configuration of antibody aldol products

Abstract:
Compounds 1-7 are the products formed by aldol condensation of p-nitrobenzaldehyde with a series of unsymmetrical ketones, the reaction occurring at the less substituted carbon. The asymmetric synthesis of 1-7 using the Evans's asymmetric aldol methodology is described in detail. These syntheses were completed to allow us to assign the absolute configuration of products 1-3, obtained in a single step in the presence of the aldolase I antibody 84G3. © 2002 Elsevier Science Ltd. All rights reserved.
Publication status:
Published

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Publisher copy:
10.1016/S0957-4166(02)00410-X

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


Journal:
TETRAHEDRON-ASYMMETRY More from this journal
Volume:
13
Issue:
16
Pages:
1789-1798
Publication date:
2002-08-27
DOI:
ISSN:
0957-4166


Language:
English
Pubs id:
pubs:38438
UUID:
uuid:0154186c-4db5-486f-8664-478d6334d8ab
Local pid:
pubs:38438
Source identifiers:
38438
Deposit date:
2012-12-19
ARK identifier:

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