Total Synthesis of (–)-Epothilone A
✍ Scribed by Dr. Aaron Balog; Dongfang Meng; Dr. Ted Kamenecka; Dr. Peter Bertinato; Dr. Dai-Shi Su; Dr. Erik J. Sorensen; Prof. Samuel J. Danishefsky
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 360 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
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The formal total synthesis of epothilone A is described. The 3 is formed by introduction of the thiazole moiety by a Wittig reaction and subsequent functional group transformation. An key steps in the synthesis of the northern hemisphere are a Z-selective ten-membered ring-closing metathesis reactio
This study was financially supported by CREST. We thank Dr. Motomu Kanai, Yoshitaka Hamashima, and Rie Namme for their support and fruitful discussion.