Literature DB >> 8582040

Tandem enzymatic resolution yielding L-alpha-aminoalkanedioic acid omega-esters.

N Nishino1, T Arai, Y Ueno, M Ohba.   

Abstract

The tandem action of serine protease (alpha-chymotrypsin or subtilisin BPN') and Aspergillus genus aminoacylase on racemic N-acetyl-alpha-aminoalkanedioic acid alpha,omega-diester produced L-alpha-aminoalkanedioic acid omega-ester in good yield and high optical purity. L-alpha-Aminosuberic acid omega-ester thus obtained was conveniently introduced into an oxytocin analog, [Asu1,6]oxytocin, by the solid-phase-synthesis and cyclization-cleavage method with oxime resin.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8582040     DOI: 10.1248/cpb.44.212

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  Synthesis of 2-aminosuberic acid derivatives as components of some histone deacetylase inhibiting cyclic tetrapeptides.

Authors:  Shital Kumar Chattopadhyay; Suman Sil; Jyoti Prasad Mukherjee
Journal:  Beilstein J Org Chem       Date:  2017-10-17       Impact factor: 2.883

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.