Literature DB >> 15103401

Biocatalytic and biomimetic aminolysis reactions: useful tools for selective transformations on polyfunctional substrates.

Ignacio Alfonso1, Vicente Gotor.   

Abstract

Aminolysis is a deeply studied reaction, but the development of new catalysts for this process is still an emerging area of organic and bioorganic chemistry. Two different approaches are reviewed in this article: the biomimetic de novo designed synthetic catalysts and the use of natural enzymes. Brief mechanistic considerations are discussed. Some important aspects like chemo-, regio- and stereoselectivity towards the substrates are highlighted on selected examples with synthetic applications.

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Year:  2004        PMID: 15103401     DOI: 10.1039/b307785n

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  4 in total

1.  Prolyl aminopeptidase from Streptomyces thermoluteus subsp. fuscus strain NBRC14270 and synthesis of proline-containing peptides by its S144C variant.

Authors:  Yukihiro Yamamoto; Hirokazu Usuki; Masaki Iwabuchi; Tadashi Hatanaka
Journal:  Appl Environ Microbiol       Date:  2010-07-30       Impact factor: 4.792

2.  One-pot synthesis of diverse DL-configuration dipeptides by a Streptomyces D-stereospecific amidohydrolase.

Authors:  Jiro Arima; Hirokazu Usuki; Tadashi Hatanaka; Nobuhiro Mori
Journal:  Appl Environ Microbiol       Date:  2011-09-23       Impact factor: 4.792

3.  Short and Efficient Synthesis of Alkyl- and Aryl-Ortho-Hydroxy-Anilides and their Antibiotic Activity.

Authors:  Jürgen Krauß; Eva Plesch; Sabine Clausen; Franz Bracher
Journal:  Sci Pharm       Date:  2014-03-13

4.  Carboxylic acid-modified metal oxide catalyst for selectivity-tunable aerobic ammoxidation.

Authors:  Xiuquan Jia; Jiping Ma; Fei Xia; Yongming Xu; Jin Gao; Jie Xu
Journal:  Nat Commun       Date:  2018-03-02       Impact factor: 14.919

  4 in total

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