Electroorganic chemistry. 82. .beta.-Amino acid esters from .alpha.-methoxycarbamates and ketene silyl acetals; cyclization to .beta.-lactams
beta -Lactams are some of the most important antibiotics, as exemplified by penicillins and cephalosporins, and hence preparation of new compounds containing a beta -lactam moiety has always attracted much attention. The authors report herein a new synthetic method of beta -lactams utilizing the rea...
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Veröffentlicht in: | Journal of organic chemistry 1984-03, Vol.49 (6), p.1056-1059 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | beta -Lactams are some of the most important antibiotics, as exemplified by penicillins and cephalosporins, and hence preparation of new compounds containing a beta -lactam moiety has always attracted much attention. The authors report herein a new synthetic method of beta -lactams utilizing the reaction of alpha -methoxylated carbamates with ketene methyl trimethylsilyl acetals as the key reaction. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/jo00180a020 |