Literature DB >> 26136142

Switching and Conformational Fixation of Amides Through Proximate Positive Charges.

Amelie L Bartuschat1, Karina Wicht1, Markus R Heinrich2.   

Abstract

Tertiary amides, which usually occur as cis/trans mixtures, can be effectively shifted to the cis conformation by placing a positive charge in close proximity to the amide carbonyl. This effect was used to prepare cis-configured prolyl amides and to facilitate a strongly rotamer-dependent radical cyclization.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  amide bond; ammonium ions; conformation; proline; rotamers

Year:  2015        PMID: 26136142     DOI: 10.1002/anie.201502474

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Modulation of Conformational Preferences of Heteroaromatic Ethers and Amides through Protonation and Ionization: Charge Effect.

Authors:  Wenshuai Dai; Zhe Zhang; Yikui Du
Journal:  ChemistryOpen       Date:  2019-06-11       Impact factor: 2.911

2.  Straightforward Access to Multifunctional π-Conjugated P-Heterocycles Featuring an Internal Ylidic Bond.

Authors:  Thomas Delouche; Elsa Caytan; Marie Cordier; Thierry Roisnel; Grégory Taupier; Yann Molard; Nicolas Vanthuyne; Boris Le Guennic; Muriel Hissler; Denis Jacquemin; Pierre-Antoine Bouit
Journal:  Angew Chem Int Ed Engl       Date:  2022-06-23       Impact factor: 16.823

  2 in total

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