Using mutability landscapes of a promiscuous tautomerase to guide the engineering of enantioselective Michaelases-Reference-Cited by-同舟云学术

Using mutability landscapes of a promiscuous tautomerase to guide the engineering of enantioselective Michaelases

Published:2016-03-08 Issue:1 Volume:7 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

van der Meer Jan-Ytzen,Poddar Harshwardhan,Baas Bert-Jan,Miao Yufeng,Rahimi Mehran,Kunzendorf Andreas,van Merkerk Ronald,Tepper Pieter G.,Geertsema Edzard M.,Thunnissen Andy-Mark W. H.,Quax Wim J.,Poelarends Gerrit J.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms10911.pdf

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3. Wiesner, M., Revell, J. D. & Wennemers, H. Tripeptides as efficient asymmetric catalysts for 1,4-addition reactions of aldehydes to nitroolefins- a rational approach. Angew. Chem. Int. Ed. Engl. 47, 1871–1874 (2008).

4. García-García, P., Ladépêche, A., Halder, R. & List, B. Catalytic asymmetric Michael ractions of acetaldehyde. Angew. Chem. Int. Ed. Engl. 47, 4719–4721 (2008).

5. Hayashi, Y., Itoh, T., Ohkubo, M. & Ishikawa, H. Asymmetric Michael reaction of acetaldehyde catalyzed by diphenylprolinol silyl ether. Angew. Chem. Int. Ed. Engl. 47, 4722–4724 (2008).

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