
Journal of the American Chemical Society p. 634 - 644 (1995)
Update date:2022-08-05
Topics:
Nicolaou
Liu
Yang
Ueno
Sorensen
Claiborne
Guy
Hwang
Nakada
Nantermet
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.
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