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A LHASA analysis of taxol

✍ Scribed by Erik L. M. van Rozendaal; Martin A. Ott; Hans W. Scheeren


Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
588 KB
Volume
113
Category
Article
ISSN
0165-0513

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✦ Synopsis


Abstract

A retrosynthetic analysis using the computer program LHASA of the promising antitumor agent taxol (1) is described, which resulted in a synthetic route with the following key steps: an intramolecular Diels‐Alder reaction generating the AB rings, and the coupling reactions of the required diene and dienophile with a CD‐ring fragment. The feasibility of the route is studied by comparing the LHASA analysis with related chemistry from the literature. Finally, a critical discussion about the usability of the LHASA program for the planning of complex organic molecules is given.]


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