Literature DB >> 27105277

Nature's Strategy for Catalyzing Diels-Alder Reaction.

Hideaki Oikawa1.   

Abstract

The enzymes catalyzing a Diels-Alder-type reaction have been attractive targets for organic chemists for years. Recently, Zheng et al. (2016) reported the structure of a formal monofunctional Diels-Alderase PyrI4 complexed with the product and unveiled a detailed catalytic mechanism of a highly important enzyme.
Copyright © 2016 Elsevier Ltd. All rights reserved.

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Year:  2016        PMID: 27105277     DOI: 10.1016/j.chembiol.2016.04.002

Source DB:  PubMed          Journal:  Cell Chem Biol        ISSN: 2451-9448            Impact factor:   8.116


  5 in total

Review 1.  Peculiarities of meroterpenoids and their bioproduction.

Authors:  Jianying Han; Lan Jiang; Lixin Zhang; Ronald J Quinn; Xueting Liu; Yunjiang Feng
Journal:  Appl Microbiol Biotechnol       Date:  2021-05-03       Impact factor: 4.813

Review 2.  Natural [4 + 2]-Cyclases.

Authors:  Byung-Sun Jeon; Shao-An Wang; Mark W Ruszczycky; Hung-Wen Liu
Journal:  Chem Rev       Date:  2016-12-01       Impact factor: 60.622

3.  Versatile Peptide Macrocyclization with Diels-Alder Cycloadditions.

Authors:  Jeffrey E Montgomery; Justin A Donnelly; Sean W Fanning; Thomas E Speltz; Xianghang Shangguan; John S Coukos; Geoffrey L Greene; Raymond E Moellering
Journal:  J Am Chem Soc       Date:  2019-09-26       Impact factor: 15.419

4.  Conceptual similarities between zeolites and artificial enzymes.

Authors:  Eva M Gallego; Cecilia Paris; Ángel Cantín; Manuel Moliner; Avelino Corma
Journal:  Chem Sci       Date:  2019-07-17       Impact factor: 9.825

5.  Intracellular Ruthenium-Promoted (2+2+2) Cycloadditions.

Authors:  Joan Miguel-Ávila; María Tomás-Gamasa; José L Mascareñas
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-11       Impact factor: 16.823

  5 in total

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