Issue 34, 2019

Triflic anhydride mediated synthesis of 3,4-dihydroquinazolines: a three-component one-pot tandem procedure

Abstract

A one-pot three-component tandem reaction involving a key Pictet–Spengler-like annulation step has been developed, providing an efficient method for the synthesis of 3,4-dihydroquinazolines in moderate to good yields from amides, aldehydes, and amines. The multicomponent triflic anhydride mediated reaction tolerates the installation of numerous functional groups, affording extensive diversity about the heterocyclic scaffold.

Graphical abstract: Triflic anhydride mediated synthesis of 3,4-dihydroquinazolines: a three-component one-pot tandem procedure

Supplementary files

Article information

Article type
Paper
Submitted
18 Jul 2019
Accepted
08 Aug 2019
First published
13 Aug 2019

Org. Biomol. Chem., 2019,17, 7995-8000

Author version available

Triflic anhydride mediated synthesis of 3,4-dihydroquinazolines: a three-component one-pot tandem procedure

C. L. Magyar, T. J. Wall, S. B. Davies, M. V. Campbell, H. A. Barna, S. R. Smith, C. J. Savich and R. A. Mosey, Org. Biomol. Chem., 2019, 17, 7995 DOI: 10.1039/C9OB01596E

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