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

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

Organic & biomolecular chemistry (2010-06-25)
Sankar K Guchhait, Chetna Madaan
RESUMEN

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.

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Sigma-Aldrich
tert-Butylamine, 98%
Sigma-Aldrich
tert-Butylamine, ≥99.5%
Sigma-Aldrich
tert-Butyl isocyanide, 98%
Sigma-Aldrich
tert-Butylamine hydrochloride, ≥98.0% (AT)