Total Synthesis of Epothilone D: The Nerol/Macroaldolization Approach

2013 ◽  
Vol 78 (21) ◽  
pp. 10588-10595 ◽  
Author(s):  
Ludger A. Wessjohann ◽  
Günther O. Scheid ◽  
Uwe Eichelberger ◽  
Sumaira Umbreen
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2001 ◽  
Vol 123 (23) ◽  
pp. 5407-5413 ◽  
Author(s):  
James D. White ◽  
Rich G. Carter ◽  
Kurt F. Sundermann ◽  
Markus Wartmann


2016 ◽  
Vol 23 (3) ◽  
pp. 541-545 ◽  
Author(s):  
Alexander M. Haydl ◽  
Bernhard Breit


ChemInform ◽  
2014 ◽  
Vol 45 (15) ◽  
pp. no-no
Author(s):  
Ludger A. Wessjohann ◽  
Günther O. Scheid ◽  
Uwe Eichelberger ◽  
Sumaira Umbreen
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2004 ◽  
Vol 1 (11) ◽  
pp. 1771-1784 ◽  
Author(s):  
Nicole End ◽  
Pascal Furet ◽  
Nathalie van?Campenhout ◽  
Markus Wartmann ◽  
Karl-Heinz Altmann


2003 ◽  
Vol 125 (10) ◽  
pp. 3190-3190 ◽  
Author(s):  
James D. White ◽  
Rich G. Carter ◽  
Kurt F. Sundermann ◽  
Markus Wartmann


2019 ◽  
Vol 14 (9) ◽  
pp. 1934578X1986859
Author(s):  
Momoko Suzuki ◽  
Shougo Hashimoto ◽  
Shun Sakamoto ◽  
Hiroshi Kogen ◽  
Kenichi Kobayashi

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.



2005 ◽  
Vol 33 (2) ◽  
pp. 116-133 ◽  
Author(s):  
Robert L. Broadrup ◽  
Hema M. Sundar ◽  
Charles S. Swindell
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2010 ◽  
Vol 51 (27) ◽  
pp. 3497-3500 ◽  
Author(s):  
Alaksiej L. Hurski ◽  
Oleg G. Kulinkovich


ChemInform ◽  
2010 ◽  
Vol 32 (38) ◽  
pp. no-no
Author(s):  
James D. White ◽  
Rich G. Carter ◽  
Kurt F. Sundermann ◽  
Markus Wartmann


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