Evidence for the Formation of an Enamine Species during Aldol and Michael-type Addition Reactions Promiscuously Catalyzed by 4-Oxalocrotonate Tautomerase-Reference-Cited by-同舟云学术

Evidence for the Formation of an Enamine Species during Aldol and Michael-type Addition Reactions Promiscuously Catalyzed by 4-Oxalocrotonate Tautomerase

Published:2015-02-26 Issue:5 Volume:16 Page:738-741
ISSN:1439-4227
Container-title:ChemBioChem
language:en
Short-container-title:ChemBioChem

Author:

Poddar Harshwardhan,Rahimi Mehran,Geertsema Edzard M.,Thunnissen Andy-Mark W. H.,Poelarends Gerrit J.

Publisher

Wiley

Subject

Organic Chemistry,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/cbic.201402687/fullpdf

Reference27 articles.

1. The chemical versatility of the β–α–β fold: Catalytic promiscuity and divergent evolution in the tautomerase superfamily

2. The 4-oxalocrotonate tautomerase family of enzymes: how nature makes new enzymes using a β–α–β structural motif

3. Physically associated enzymes produce and metabolize 2-hydroxy-2,4-dienoate, a chemically unstable intermediate formed in catechol metabolism via meta cleavage in Pseudomonas putida

4. Chemical and enzymic ketonization of 2-hydroxymuconate, a conjugated enol

5. 4-Oxalocrotonate Tautomerase: pH Dependence of Catalysis and pKa Values of Active Site Residues

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