Issue 21, 2014

Trifluoroacetic acid-promoted Michael addition–cyclization reactions of vinylogous carbamates

Abstract

A simple and efficient methodology has been developed for the synthesis of pyrrolobenzoxazine and 3-arylamino coumarin derivatives promoted by trifluoroacetic acid. The initial step in the current protocol involves a Michael addition of the 1,4-benzoxazinone derivatives, a novel class of vinylogous carbamates to the Michael acceptors and subsequent cyclization.

Graphical abstract: Trifluoroacetic acid-promoted Michael addition–cyclization reactions of vinylogous carbamates

Supplementary files

Article information

Article type
Communication
Submitted
26 Feb 2014
Accepted
18 Mar 2014
First published
22 Apr 2014

Org. Biomol. Chem., 2014,12, 3366-3370

Author version available

Trifluoroacetic acid-promoted Michael addition–cyclization reactions of vinylogous carbamates

R. T. Naganaboina, A. Nayak and R. K. Peddinti, Org. Biomol. Chem., 2014, 12, 3366 DOI: 10.1039/C4OB00437J

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