Literature DB >> 17989487

3-Oxo-5beta-24-norcholanic acid: acid-to-acid hydrogen-bonding catemers employing the rare anti carboxyl conformation in the aggregation of a steroid keto acid.

Marisa DeVita Dufort1, Mark Davison, Roger A Lalancette, Hugh W Thompson.   

Abstract

The title ketocarboxylic acid [systematic name: (5R,8R,9S,10S,13R,14S,17R,20R)-3-oxo-24-norcholanic acid], C(23)H(36)O(3), forms acid-to-acid hydrogen-bonding chains [O...O = 2.620 (2) A and O-H...O = 163 (3) degrees ] in which all carboxyl groups adopt the rare anti conformation, while the ketone group does not participate in the hydrogen bonding. The occurrence and energetics of this conformation are discussed. One intermolecular C-H...O close contact exists, which plays a role in stabilizing the hydrogen-bonding arrangement.

Entities:  

Year:  2007        PMID: 17989487     DOI: 10.1107/S0108270107047014

Source DB:  PubMed          Journal:  Acta Crystallogr C        ISSN: 0108-2701            Impact factor:   1.172


  2 in total

1.  (±)-2-Oxocyclo-penta-neacetic acid: catemeric hydrogen bonding in a γ-keto acid.

Authors:  Georgia Efthimiopoulos; Markos M Papadakis; Hugh W Thompson; Roger A Lalancette
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-03-31

2.  A comprehensive classification and nomenclature of carboxyl-carboxyl(ate) supramolecular motifs and related catemers: implications for biomolecular systems.

Authors:  Luigi D'Ascenzo; Pascal Auffinger
Journal:  Acta Crystallogr B Struct Sci Cryst Eng Mater       Date:  2015-03-24
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.