Literature DB >> 32852088

Artificial Enzymes for Diels-Alder Reactions.

Wadih Ghattas1, Jean-Pierre Mahy1, Marius Réglier2, A Jalila Simaan2.   

Abstract

The Diels-Alder (DA) reaction is a cycloaddition of a conjugated diene and an alkene (dienophile) leading to the formation of a cyclohexene derivative through a concerted mechanism. As DA reactions generally proceed with a high degree of regio- and stereoselectivity, they are widely used in synthetic organic chemistry. Considering eco-conscious public and governmental movements, efforts are now directed towards the development of synthetic processes that meet environmental concerns. Artificial enzymes, which can be developed to catalyze abiotic reactions, appear to be important synthetic tools in the synthetic biology field. This review describes the different strategies used to develop protein-based artificial enzymes for DA reactions, including for in cellulo approaches.
© 2020 Wiley-VCH GmbH.

Entities:  

Keywords:  Diels-Alder; artificial enzymes; artificial metalloenzymes; catalytic antibodies; de novo design

Year:  2020        PMID: 32852088     DOI: 10.1002/cbic.202000316

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  3 in total

1.  Mechanism of the Stereoselective Catalysis of Diels-Alderase PyrE3 Involved in Pyrroindomycin Biosynthesis.

Authors:  Bo Li; Xingyi Guan; Song Yang; Yike Zou; Wen Liu; K N Houk
Journal:  J Am Chem Soc       Date:  2022-03-08       Impact factor: 16.383

Review 2.  Lessons in Organic Fluorescent Probe Discovery.

Authors:  Sachin B Wagh; Vladimir A Maslivetc; James J La Clair; Alexander Kornienko
Journal:  Chembiochem       Date:  2021-06-23       Impact factor: 3.164

Review 3.  Redesigning Enzymes for Biocatalysis: Exploiting Structural Understanding for Improved Selectivity.

Authors:  Yaoyu Ding; Gustavo Perez-Ortiz; Jessica Peate; Sarah M Barry
Journal:  Front Mol Biosci       Date:  2022-07-22
  3 in total

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