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Evidence for an insertion-homolysis mechanism for carbon-sulphur bond formation in penicillin biosynthesis .1. Synthesis of tripeptide probes

Baldwin, JE; Adlington, RM; Marquess, DG; Pitt, AR; Porter, MJ; Russell, AT; (1996) Evidence for an insertion-homolysis mechanism for carbon-sulphur bond formation in penicillin biosynthesis .1. Synthesis of tripeptide probes. TETRAHEDRON , 52 (7) 2515 - 2536.

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Abstract

Synthesis of four LLD-ACV analogues, in which the valine residue has been replaced by an amino acid containing a stereospecifically deuterated cyclopropane ring, is described.

Type:Article
Title:Evidence for an insertion-homolysis mechanism for carbon-sulphur bond formation in penicillin biosynthesis .1. Synthesis of tripeptide probes
Keywords:CYCLOPROPYLCARBINYL, ALCOHOLS, STEREOCHEMISTRY, CEPHALOSPORINS, ALLYLCARBINYL, ACID
UCL classification:UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry

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