Penicillin biosynthesis. A model for carbon–sulphur bond formation
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1979/C3/C39790000249
Cited by 36 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Free-Radical Reactions in the Synthesis of α-Amino Acids and Derivatives;Chemical Reviews;1997-02-01
2. Tris(trimethylsilyl)silyl Radical Induced Bicyclization of 1,6-Dienes and 1,6-Enynes Providing 3,3-Bis(trimethylsilyl)-3-silabicyclo[3.3.0]octanes and 3-Silabicyclo[3.3.0]oct-1-enes;Bulletin of the Chemical Society of Japan;1993-08
3. Intramolecular radical substitution on the sulfur of thioester, sulfide, sulfoxide, and sulfone;Tetrahedron Letters;1992-10
4. Enzymic conversion of deuterated analogues of δ--α-aminoadipoyl--cysteinyl--allylglycine, an unnatural substrate for isopenicilin n synthase: A unified theory of second ring closure.;Tetrahedron;1991-09
5. Radical substitution on the sulphur of thioester group;Journal of the Chemical Society, Chemical Communications;1990
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