Abstract
A method for the formation of Taxol's ABC ring system has been developed. General methods for the synthesis of versatile synthons for Taxol's A ring (8) and C ring (55) are presented. A model study using a simplified C ring synthon (17) confirmed the viability of the sequential Shapiro—McMurry strategy for formation of Taxol's B ring. Careful exploration of the chemistry of various A—B ring conjugates allowed the development of a successful method for formation of the B ring in a more functionalized system.
Original language | English |
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Pages (from-to) | 634-644 |
Number of pages | 11 |
Journal | Journal of the American Chemical Society |
Volume | 117 |
Issue number | 2 |
DOIs | |
State | Published - Jan 1995 |
ASJC Scopus subject areas
- Catalysis
- General Chemistry
- Biochemistry
- Colloid and Surface Chemistry