Biocatalytic transamination with near-stoichiometric inexpensive amine donors mediated by bifunctional mono- and di-amine transaminases-Reference-Cited by-同舟云学术

Biocatalytic transamination with near-stoichiometric inexpensive amine donors mediated by bifunctional mono- and di-amine transaminases

Published:2017 Issue:2 Volume:19 Page:361-366
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Galman James L.¹²³⁴⁵,Slabu Iustina¹²³⁴⁵,Weise Nicholas J.¹²³⁴⁵,Iglesias Cesar⁶⁷⁸⁹,Parmeggiani Fabio¹²³⁴⁵,Lloyd Richard C.¹⁰¹¹¹²⁵,Turner Nicholas J.¹²³⁴⁵^ORCID

Affiliation:

1. Manchester Institute of Biotechnology (MIB)

2. School of Chemistry

3. The University of Manchester

4. Manchester

5. UK

6. Facultad de Quimica

7. Universidad de la República

8. Montevideo

9. Uruguay

10. Dr. Reddy's Laboratories

11. Chirotech Technology Centre

12. Cambridge

Abstract

Bifunctional transaminases enable a strategy for the production of chiral amines using small excesses of diamine donors.

Funder

European Commission

Biotechnology and Biological Sciences Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/GC/C6GC02102F

Reference27 articles.

1. Biocatalytic retrosynthesis

2. How Green is Biocatalysis? To Calculate is To Know

3. Biocatalytic Asymmetric Synthesis of Chiral Amines from Ketones Applied to Sitagliptin Manufacture

4. Process considerations for the asymmetric synthesis of chiral amines using transaminases

5. Rapid screening and scale-up of transaminase catalysed reactions

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