The tert-Butyl Side Chain: A Powerful Means to Lock Peptoid Amide Bonds in the Cis Conformation - Université de Lorraine
Article Dans Une Revue Organic Letters Année : 2013

The tert-Butyl Side Chain: A Powerful Means to Lock Peptoid Amide Bonds in the Cis Conformation

Résumé

The very simple sterically hindered tert-butyl side chain exerts complete control over the peptoid amide geometry which only exists in the cis conformation. It is exemplified in NtBu glycine homo-oligomers and in linear oligopeptoids designed with an alternating cis-trans backbone amide pattern.

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Cristallographie
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Dates et versions

hal-01520992 , version 1 (11-05-2017)

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Citer

O. Roy, C. Caumes, Y. Esvan, Claude Didierjean, S. Faure, et al.. The tert-Butyl Side Chain: A Powerful Means to Lock Peptoid Amide Bonds in the Cis Conformation. Organic Letters, 2013, 15 (9), pp.2246-2249. ⟨10.1021/ol400820y⟩. ⟨hal-01520992⟩
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