| Literature DB >> 26136142 |
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.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