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Stereochemistry of hydride reductions. The tricyclo[9.3.1.0.3,8]pentadecane (taxane) ring system

✍ Scribed by K.J. Shea; Richard G. Higby; Jeffrey W. Gilman


Publisher
Elsevier Science
Year
1990
Tongue
French
Weight
253 KB
Volume
31
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


The Tricyclo[9.3.1.03,8]pentadecane Syst
✍ Prof. Dr. Kenneth J. Shea; Dr. Peter D. Davis πŸ“‚ Article πŸ“… 1983 πŸ› John Wiley and Sons 🌐 English βš– 235 KB

ture and oxygen over a long period of time[4a1. It was also obtained by reaction of 4 with elemental sulfur (60% yield). Reaction of 2 with chlorine affords 2,4,6-tri-tert-butylphenyfphosphonic dichloride almost quantitatively after hydrolysis'za1. The yields of compounds 2, 3[4b1, and 4 (20-60%, 1

An Enantioselective Approach to the Taxa
✍ Leo A. Paquette; Steven W. Elmore; Keith D. Combrink; Eugene R. Hickey; Robin D. πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 German βš– 999 KB

## Abstract The feasibility of the titled reactions for the rapid, enantioselective synthesis of __cis__‐tricyclo[9.3.1.0^3,8^]pentadecane precursors to taxusin and taxol has been examined. The catalysts most well suited to inducing the appropriate 1,2‐shifts have been identified. To a great extent