Sequential N-acylamide methylenation-enamide ring-closing metathesis: A synthetic entry to 1,4-dihydroquinolines

37Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.
Get full text

Abstract

A new synthetic entry to the 1,4-dihydroquinoline nucleus is reported. The procedure involves the dimethyltitanocene methylenation of N-(alkoxycarbonyl) amides derived from 2-allylanilines, followed by ring-closing metathesis of the resulting enamides. © 2005 Elsevier Ltd. All rights reserved.

Cite

CITATION STYLE

APA

Bennasar, M. L., Roca, T., Monerris, M., & García-Díaz, D. (2005). Sequential N-acylamide methylenation-enamide ring-closing metathesis: A synthetic entry to 1,4-dihydroquinolines. Tetrahedron Letters, 46(23), 4035–4038. https://doi.org/10.1016/j.tetlet.2005.04.028

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free