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The Olefin Metathesis Approach to Epothilone A and Its Analogues

✍ Scribed by Nicolaou, K. C.; He, Y.; Vourloumis, D.; Vallberg, H.; Roschangar, F.; Sarabia, F.; Ninkovic, S.; Yang, Z.; Trujillo, J. I.

Book ID
121467668
Publisher
American Chemical Society
Year
1997
Tongue
English
Weight
560 KB
Volume
119
Category
Article
ISSN
0002-7863

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ChemInform Abstract: Total Synthesis of
ChemInform Abstract: Total Synthesis of Oxazole- and Cyclopropane-Containing Epothilone A Analogues by the Olefin Metathesis Approach.
✍ K. C. NICOLAOU; H. VALLBERG; N. P. KING; F. ROSCHANGAR; Y. HE; D. VOURLOUMIS; C. πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 39 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

ChemInform Abstract: Total Synthesis of
ChemInform Abstract: Total Synthesis of Epothilone A: The Olefin Metathesis Approach.
✍ Z. YANG; Y. HE; D. VOURLOUMIS; H. VALLBERG; K. C. NICOLAOU πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 29 KB πŸ‘ 1 views

Total Synthesis of Epothilone A: The Olefin Metathesis Approach. -Starting with the three building blocks (I)-(III) the coupling product (IV) is obtained. It is used for olefin metathesis as the key step in the synthesis of the title compound (VI). -(YANG, Z.;