Total Synthesis of 16-Desmethylepothilone B, Epothilone B 10, Epothilone F, and Related Side Chain Modified Epothilone B Analogues

Autor: Nicolaou, K. C., Hepworth, David, King, N. Paul, Finlay, M. Raymond V., Scarpelli, Rita, Pereira, M. Manuela A., Bollbuck, Birgit, Bigot, Antony, Werschkun, Barbara, Winssinger, Nicolas
Jazyk: angličtina
Rok vydání: 2000
Předmět:
Zdroj: Chemistry-A European Journal, Vol. 6, No 15 (2000) pp. 2783-2800
ISSN: 0947-6539
Popis: The macrolactonization-based strategy for the total synthesis of epothilones has been streamlined and improved to a high level of efficiency and stereoselectivity. This strategy has been applied to the construction of vinyl iodide 19 which served as a common intermediate for the synthesis of a series of natural and designed epothilones including an epothilone B10 (3), epothilone F (5), 16-desmethylepothilone B (14), pyridine epothilones 57 a–57 g, dimeric epothilones 59 and 61, and benzenoid epothilones 63 a–63 g.
Databáze: OpenAIRE