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A facile synthesis of benzyl 3,7-dioxo-1-azabicyclo[3.2.0]Heptane-2-carboxylate. A potential precursor of thienamycin and clavulanic acid analogs

✍ Scribed by D.A. Berges; E.R. Snipes; G.W. Chan; W.D. Kingsbury; C.M. Kinzig


Publisher
Elsevier Science
Year
1981
Tongue
French
Weight
198 KB
Volume
22
Category
Article
ISSN
0040-4039

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✦ Synopsis


A novel, high yield synthesis of the l-carbapenam ring system J, is described in which the entire carbon framework is introduced in a single step from simple precursors.

Thienamycin (A) and clavulanic acid (L), new naturally occurring B-lactams


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