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

DOI: 10.1016/0040-4020(95)01071-8

Source and publish data:

Tetrahedron p. 2515 - 2536 (1996)

Update date:2022-08-05

Topics:

Authors:

Baldwin, Jack E.

Adlington, Robert M.

Marquess, Daniel G.

Pitt, Andrew R.

Porter, Michael J.

Russell, Andrew T.

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Article abstract of DOI:10.1016/0040-4020(95)01071-8

Synthesis of four LLD-ACV analogues, in which the valine residue has been replaced by an amino acid containing a stereospecifically deuterated cyclopropane ring, is described.

Full text of DOI:10.1016/0040-4020(95)01071-8

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