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Stereocontrolled synthesis of the key intermediate for the enantioselective synthesis of clerodane natural products

✍ Scribed by Michiharu Kato; Hiroshi Kosugi; Ariko Kodaira; Hisahiro Hagiwara; Bernhard Vogler


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
218 KB
Volume
38
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Stereocontrolled Sy
✍ M. KATO; H. KOSUGI; A. KODAIRA; H. HAGIWARA; B. VOGLER πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 26 KB πŸ‘ 2 views

## 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

Stereocontrolled route to a key intermed
✍ E.J. Corey; Mark G. Bock πŸ“‚ Article πŸ“… 1975 πŸ› Elsevier Science 🌐 French βš– 210 KB

We have undertaken a synthesis of this substance as part of a broader program in the area of biologically active macrocyclic natural products. One attractive approach to the synthesis of maytansine involves the introduction of chiraltty at carbons 3, 4, 5, 10, and 9 after formation of the macro ring