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3-氧代-5β-24-降胆烷酸:在甾体酮酸聚集过程中采用罕见反式羧基构象的酸-酸氢键二聚体。

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.

作者信息

DeVita Dufort Marisa, Davison Mark, Lalancette Roger A, Thompson Hugh W

机构信息

Carl A. Olson Memorial Laboratories, Department of Chemistry, Rutgers University, Newark, NJ 07102, USA.

出版信息

Acta Crystallogr C. 2007 Nov;63(Pt 11):o646-9. doi: 10.1107/S0108270107047014. Epub 2007 Oct 13.

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.

摘要

标题酮羧酸[系统名称:(5R,8R,9S,10S,13R,14S,17R,20R)-3-氧代-24-降胆烷酸],C(23)H(36)O(3),形成酸-酸氢键链[O...O = 2.620(2)Å,O-H...O = 163(3)°],其中所有羧基均采用罕见的反式构象,而酮基不参与氢键形成。讨论了这种构象的出现和能量情况。存在一个分子间C-H...O紧密接触,它在稳定氢键排列中起作用。

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