Stereoselective C–C bond formation catalysed by engineered carboxymethylproline synthases-Reference-Cited by-同舟云学术

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Stereoselective C–C bond formation catalysed by engineered carboxymethylproline synthases

Published:2011-04-03 Issue:5 Volume:3 Page:365-371
ISSN:1755-4330
Container-title:Nature Chemistry
language:en
Short-container-title:Nature Chem

Author:

Hamed Refaat B.,Gomez-Castellanos J. Ruben,Thalhammer Armin,Harding Daniel,Ducho Christian,Claridge Timothy D. W.,Schofield Christopher J.

Publisher

Springer Science and Business Media LLC

Subject

General Chemical Engineering,General Chemistry

Link

http://www.nature.com/articles/nchem.1011.pdf

Reference22 articles.

1. Schultz, P. & Lerner, R. From molecular diversity to catalysis: lessons from the immune system. Science 269, 1835–1842 (1995).

2. Reymond, J. Stereoselectivity of aldolase catalytic antibodies. J. Mol. Catal. B 5, 331–337 (1998).

3. Dean, S., Greenberg, W. & Wong, C. Recent advances in aldolase-catalyzed asymmetric synthesis. Adv. Synth. Catal. 349, 1308–1320 (2007).

4. Bolt, A., Berry, A. & Nelson, A. Directed evolution of aldolases for exploitation in synthetic organic chemistry. Arch. Biochem. Biophys. 474, 318–330 (2008).

5. Hamed, R. B., Batchelar, E. T., Clifton, I. J. & Schofield, C. J. Mechanisms and structures of crotonase superfamily enzymes—how nature controls enolate and oxyanion reactivity. Cell. Mol. Life Sci. 65, 2507–2527 (2008).

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