Title of article
Sequential N-acylamide methylenation–enamide ring-closing metathesis: a synthetic entry to 1,4-dihydroquinolines
Author/Authors
Bennasar، نويسنده , , M.-Lluïsa and Roca، نويسنده , , Tomàs and Monerris، نويسنده , , Manuel and Garcيa-Dيaz، نويسنده , , Davinia، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
4
From page
4035
To page
4038
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.
Keywords
Enamides , Olefination , ring-closing metathesis , 4-Dihydroquinolines , Dimethyltitanocene , 1
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1845875
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