Issue 2, 2015

General base-tuned unorthodox synthesis of amides and ketoesters with water

Abstract

We discovered a highly reactive λ3-hypervalent iodane species using an inorganic/organic base for the unorthodox synthesis of amides and ketoesters through grafting terminal alkynes. In contrast to the metal-catalyzed dehydrative approaches the in situ generated nonmetallic reagent efficiently created C–N/C–O and C[double bond, length as m-dash]O bonds with amines/alkynes and water at rt.

Graphical abstract: General base-tuned unorthodox synthesis of amides and ketoesters with water

Supplementary files

Article information

Article type
Communication
Submitted
08 Oct 2014
Accepted
10 Nov 2014
First published
11 Nov 2014

Chem. Commun., 2015,51, 384-387

Author version available

General base-tuned unorthodox synthesis of amides and ketoesters with water

S. Khamarui, R. Maiti and D. K. Maiti, Chem. Commun., 2015, 51, 384 DOI: 10.1039/C4CC07961B

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