Issue 16, 2010

Towards molecular diversity: dealkylation of tert-butyl amine in Ugi-type multicomponent reaction product establishes tert-butyl isocyanide as a useful convertible isonitrile

Abstract

With the development of a novel microwave-assisted one-pot tandem de-tert-butylation of tert-butyl amine in an Ugi-type multicomponent reaction product, tert-butyl isocyanide as a useful convertible isonitrile has been explored for the first time affording access to molecular diversity of pharmaceutically-important polycyclic N-fused imidazo-heterocycles.

Graphical abstract: Towards molecular diversity: dealkylation of tert-butyl amine in Ugi-type multicomponent reaction product establishes tert-butyl isocyanide as a useful convertible isonitrile

Supplementary files

Article information

Article type
Communication
Submitted
20 Apr 2010
Accepted
09 Jun 2010
First published
24 Jun 2010

Org. Biomol. Chem., 2010,8, 3631-3634

Towards molecular diversity: dealkylation of tert-butyl amine in Ugi-type multicomponent reaction product establishes tert-butyl isocyanide as a useful convertible isonitrile

S. K. Guchhait and C. Madaan, Org. Biomol. Chem., 2010, 8, 3631 DOI: 10.1039/C0OB00022A

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