The acid-mediated ring opening/cyclisation reaction of N-benzyl-α-aryl-azetidinones
2012
King, Frank D. | Caddick, Stephen
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.
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Bibliographic information
Publisher
Elsevier Ltd
Language
English
Type
Journal Article; Text
2024-02-28
MODS
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