The C( 1)-C(9) segment 3 of the macrolides epothilon A and B 1, two new cytotoxic natural products, has been synthesized in a direct manner. Key steps in the synthesis are a stereoselective aldol reaction of 6 and 7 and a Brown allylation of 9.
✦ LIBER ✦
Synthetic studies on cytotoxic macrolides cruentarens A and B: stereoselective synthesis of the C8–C19 segment of cruentarens A and B
✍ Scribed by Busam Ramalinga Vara Prasad; Harshadas Mitaram Meshram
- Book ID
- 108284582
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 411 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0957-4166
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