Title of article
The acid-mediated ring opening/cyclisation reaction of N-benzyl-α-aryl-azetidinones
Author/Authors
Frank D. King، نويسنده , , Stephen Caddick، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2012
Pages
5
From page
9350
To page
9354
Abstract
N-Benzyl-4-aryl-azetidinones undergo ring opening with triflic acid to form N-benzyl-cinnamamides, which either undergo cyclisation to give 5-aryl-benzazepin-3-ones or N-debenzylation to give cinnamamides.
Keywords
Triflic acid , intramolecular cyclisation , Benzazepin-3-ones , azetidinone , cinnamamides
Journal title
Tetrahedron
Serial Year
2012
Journal title
Tetrahedron
Record number
1105113
Link To Document