Literature DB >> 22292802

(S)-ABOC: a rigid bicyclic β-amino acid as turn inducer.

Christophe André1, Baptiste Legrand, Cheng Deng, Claude Didierjean, Guillaume Pickaert, Jean Martinez, Marie Christine Averlant-Petit, Muriel Amblard, Monique Calmes.   

Abstract

In order to investigate the ability of the (S)-aminobicyclo[2.2.2]octane-2-carboxylic acid 1 (H-(S)-ABOC-OH) to induce reverse turns into peptides, two model tripeptides, in which this bicyclic unit was incorporated into the second position, were synthesized and analyzed by FT-IR, CD, NMR, and X-ray studies.

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Year:  2012        PMID: 22292802     DOI: 10.1021/ol203406v

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Turn-folding in fluorescent anthracene-substituted cyclopenta[d]isoxazoline short peptides.

Authors:  Marco Leusciatti; Barbara Mannucci; Teresa Recca; Paolo Quadrelli
Journal:  RSC Adv       Date:  2021-06-01       Impact factor: 4.036

Review 2.  Asymmetric Catalysis Mediated by Synthetic Peptides, Version 2.0: Expansion of Scope and Mechanisms.

Authors:  Anthony J Metrano; Alex J Chinn; Christopher R Shugrue; Elizabeth A Stone; Byoungmoo Kim; Scott J Miller
Journal:  Chem Rev       Date:  2020-09-24       Impact factor: 60.622

3.  Crystal structure of Boc-(S)-ABOC-(S)-Ala-(S)-ABOC-(S)-Phe-OBn chloro-form monosolvate.

Authors:  Emmanuel Wenger; Laure Moulat; Baptiste Legrand; Muriel Amblard; Monique Calmès; Claude Didierjean
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2015-09-17
  3 in total

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