Literature DB >> 21688328

Synthesis and C(2) -symmetric structure of a cyclotetrapeptide composed of anthranilic acid and leucine.

Motohiro Akazome1, Masashi Enzu, Koji Takagi, Shoji Matsumoto.   

Abstract

A chiral cyclotetrapeptide (1) was synthesized from 2-nitrobenzoic acid and leucine. A single-crystal X-ray of the compound revealed a C(2) -symmetric bowl-shaped structure. The cyclic compound had a unique hydrogen-bonding network composed of three-centered hydrogen bonds and bifurcated hydrogen bonds between NH and CO of anthranilic residue. The NMR spectra and molecular modeling of 1 also suggested the chiral bowl structure.
Copyright © 2011 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21688328     DOI: 10.1002/chir.20972

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  2 in total

1.  Anthranilic acid-containing cyclic tetrapeptides: at the crossroads of conformational rigidity and synthetic accessibility.

Authors:  Dongyue Xin; Kevin Burgess
Journal:  Org Biomol Chem       Date:  2016-05-13       Impact factor: 3.876

2.  The multicomponent approach to N-methyl peptides: total synthesis of antibacterial (-)-viridic acid and analogues.

Authors:  Ricardo A W Neves Filho; Sebastian Stark; Bernhard Westermann; Ludger A Wessjohann
Journal:  Beilstein J Org Chem       Date:  2012-11-28       Impact factor: 2.883

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.