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Synthesis and antimicrobial activity of 4-amino trinems
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 s...
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Published in: | Bioorganic & medicinal chemistry letters 1996-07, Vol.6 (14), p.1683-1688 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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.
The synthesis of 4-amino substituted trinems
1 starting from the epoxy intermediate
2 is described. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/0960-894X(96)00292-2 |