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Determination of the stereochemistry of tritium label in sulbactam obtained by isotope exchange of penicillanic acid (R)-sulphoxide benzyl ester

✍ Scribed by Colin L. Gibson; John R. Jones; Andrew P. Sharratt; Robert H. Liss


Publisher
John Wiley and Sons
Year
1991
Tongue
French
Weight
268 KB
Volume
29
Category
Article
ISSN
0022-2135

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✦ Synopsis


Abstract

Sulbactam, a β‐lactamase inhibitor, has been prepared in tritiated (170 mCi mmol^−1^) form by the highly stereospecific isotope exchange procedure involving penicillanic acid (R)‐sulphoxide benzyl ester. The stereochemistry of the tritiation has been established by ^3^H n.m.r. in conjunction with a ^1^H NOESY spectrum of sulbactam.