Amidation of unactivated ester derivatives mediated by trifluoroethanol. Issue 16 (10th April 2017)

• Record Type: Journal Article
• Authors: McPherson, Christopher G.; Caldwell, Nicola; Jamieson, Craig; Simpson, Iain; Watson, Allan J. B.
• Is Part Of: Organic & biomolecular chemistry. Volume 15:Issue 16(2017)
• Page Start: 3507
• Page End: 3518
• Publication Date: 2017-04-10
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/c7ob00593h
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : A catalytic amidation protocol mediated by 2, 2, 2-trifluoroethanol has been developed, facilitating the condensation of unactivated esters and amines, furnishing both secondary and tertiary amides. Abstract : A catalytic amidation protocol mediated by 2, 2, 2-trifluoroethanol has been developed, facilitating the condensation of unactivated esters and amines, furnishing both secondary and tertiary amides. The complete scope and limitations of the method are described, along with modified conditions for challenging substrates such as acyclic secondary amines and chiral esters with retention of chiral integrity.