Studies toward the Total Synthesis of Epothilone D: Synthesis of the Thiazole-Containing Northern Segment
Momoko Suzuki, Shougo Hashimoto, Shun Sakamoto, Hiroshi Kogen, Kenichi Kobayashi
Abstract
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Momoko Suzuki, Shougo Hashimoto, Shun Sakamoto, Hiroshi Kogen, Kenichi Kobayashi
Abstract
Open-access reader
Epothilone D, a microtubule-stabilizing macrolide, is an attractive synthetic target molecule as a potential anti-cancer drug candidate. As part of our ongoing synthetic studies of this natural product, this paper describes the synthesis of the thiazole-containing northern segment of epothilone D via an E-selective bromomethylenation and a Ni/Cr-mediated cross-coupling reaction.
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Epothilone D, a microtubule-stabilizing macrolide, is an attractive synthetic target molecule as a potential anti-cancer drug candidate. As part of our ongoing synthetic studies of this natural product, this paper describes the synthesis of the thiazole-containing northern segment of epothilone D via an E-selective bromomethylenation and a Ni/Cr-mediated cross-coupling reaction.
Key concepts: Thiazole, Epothilone, Natural product, Stereochemistry, Epothilones, Chemistry, Combinatorial chemistry, Total synthesis