Journal article

A biocatalytic route to enantioenriched, sulfanyl aldol products

Abstract:: The aldol products derived from sulfur- or selenium containing acceptors were prepared by kinetic resolution in the presence of antibody 84G3 with enantiomeric excesses ranging from 56 to 70%. Much higher level of enantioselectivity was obtained (enantiomeric excesses all superior to 96%) for sulfanyl aldol products derived from thiomethoxyacetone with three different acceptors. © 2004 Elsevier Ltd. All rights reserved.

Publication status:: Published

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APA Style

Baker-Glenn, C., Ancliff, R., & Gouverneur, V. (2004). A biocatalytic route to enantioenriched, sulfanyl aldol products. TETRAHEDRON, 60(35), 7607–7619.

MLA Style

Baker-Glenn, C., et al. “A Biocatalytic Route to Enantioenriched, Sulfanyl Aldol Products.” TETRAHEDRON, vol. 60, no. 35, 2004, pp. 7607–19.

Chicago Style

Baker-Glenn, C, R Ancliff, and V Gouverneur. 2004. “A Biocatalytic Route to Enantioenriched, Sulfanyl Aldol Products.” TETRAHEDRON 60 (35): 7607–19.
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Publisher copy:: 10.1016/j.tet.2004.06.033

Authors

+ Baker-Glenn, C More by this author

Role:: Author

+ Ancliff, R More by this author

Role:: Author

+ Gouverneur, V More by this author

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

Journal:: TETRAHEDRON More from this journal
Volume:: 60
Issue:: 35
Pages:: 7607-7619
Publication date:: 2004-08-23
DOI:: 10.1016/j.tet.2004.06.033
ISSN:: 0040-4020

Language:: English
Keywords:: aldol additon

catalytic antibodies

sulfur
Pubs id:: pubs:39123
UUID:: uuid:4d6d5fb6-859c-41b9-966e-9adc45a8b5b6
Local pid:: pubs:39123
Source identifiers:: 39123
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2004

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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