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An Efficient Synthesis of Epoxydiynes and a Key Fragment of Neocarzinostatin Chromophore

✍ Scribed by Baker, J. R.; Thominet, O.; Britton, H.; Caddick, S.


Book ID
127159385
Publisher
American Chemical Society
Year
2007
Tongue
English
Weight
65 KB
Volume
9
Category
Article
ISSN
1523-7060

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πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Total Synthesis of
✍ A. G. MYERS; J. LIANG; M. HAMMOND; P. M. HARRINGTON; Y. WU; E. Y. KUO πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB πŸ‘ 2 views

Total Synthesis of (+)-Neocarzinostatin Chromophore. -The optimized route to the desired antibiotic involves an atypical protocol for the introduction of the amino sugar containing an unprotected N-methylamino group and the removal of all silyl protective groups in a single operation after glycosyl

ChemInform Abstract: Enantioselective Sy
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

Stereoselective synthesis of a functiona
✍ Stephen Caddick; Vern M. Delisser πŸ“‚ Article πŸ“… 1997 πŸ› Elsevier Science 🌐 French βš– 316 KB

The sterem&ctive synthesis of a bicyclic ring system related to Neocarzinostatin and Kedarcidin Chromophonzs is described; key steps involve stereoselective conjugate addition of an enediyne to an enone and intramolecular aldol reaction of a cobalt complexed allcynyl aIdehyde. 0 1997 Elsevier Scienc