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A stereoselective intramolecular Diels–Alder strategy for the tricyclo[9.3.1.03,8]pentadecane core of aromatic C-ring taxanes

✍ Scribed by David V Smil; Alain Laurent; Nidejda S Spassova; Alex G Fallis


Publisher
Elsevier Science
Year
2003
Tongue
French
Weight
148 KB
Volume
44
Category
Article
ISSN
0040-4039

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📜 SIMILAR VOLUMES


The Tricyclo[9.3.1.03,8]pentadecane Syst
✍ Prof. Dr. Kenneth J. Shea; Dr. Peter D. Davis 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 English ⚖ 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