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
Hauptverfasser: Shono, Tatsuya, Tsubata, Kenji, Okinaga, Nobuyuki
Format: Artikel
Sprache:eng
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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.
ISSN:0022-3263
1520-6904
DOI:10.1021/jo00180a020