
Bioorganic and Medicinal Chemistry Letters p. 1683 - 1688 (1996)
Update date:2022-08-03
Topics:
Tranquillini, Maria Elvira
Araldi, Gian Luca
Donati, Daniele
Pentassuglia, Giorgio
Pezzoli, Anna
Ursini, Antonella
This article deals with the study carried out on the synthesis of 4-amino substituted trinems 1 starting from the key-intermediate (3S, 4R)-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-4-[(1'R, 2'S, 3'R)-1',2'-epoxycyclohex-3'-yl]azetidin-2-one 2. In particular, epoxide opening with various amines and subsequent cyclization to the corresponding trinems were explored. Their synthesis and antimicrobial activity are reported.
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