Total Synthesis of Epothilone B, Epothilone D, andcis- andtrans-9,10-Dehydroepothilone D

2001 ◽  
Vol 123 (23) ◽  
pp. 5407-5413 ◽  
Author(s):  
James D. White ◽  
Rich G. Carter ◽  
Kurt F. Sundermann ◽  
Markus Wartmann
Keyword(s):  
Total Synthesis ◽  
Epothilone B ◽  
Epothilone D

scholarly journals Total Synthesis of Epothilone B, Epothilone D, andcis- andtrans-9,10-Dehydroepothilone D  [J. Am. Chem. Soc.2001,123, 5407−5413]. 

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

ChemInform Abstract: Total Synthesis of Epothilone B, Epothilone D, and cis- and trans-9,10-Dehydroepothilone D.

ChemInform ◽  
2010 ◽  
Vol 32 (38) ◽  
pp. no-no
Author(s):  
James D. White ◽  
Rich G. Carter ◽  
Kurt F. Sundermann ◽  
Markus Wartmann
Keyword(s):  
Total Synthesis ◽  
Epothilone B ◽  
Epothilone D ◽  
Cis And Trans

Total Synthesis of(–)-Epothilone B: An Extension of the Suzuki Coupling Method and Insights into Structure–Activity Relationships of the Epothilones

1997 ◽  
Vol 36 (7) ◽  
pp. 757-759 ◽  
Author(s):  
Dai-Shi Su ◽  
Dongfang Meng ◽  
Peter Bertinato ◽  
Aaron Balog ◽  
Erik J. Sorensen ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Suzuki Coupling ◽  
Coupling Method ◽  
Structure Activity Relationships ◽  
Epothilone B ◽  
Structure Activity

The Keck Synthesis of Epothilone B

2011 ◽  
Author(s):  
Douglass Taber
Keyword(s):  
Total Synthesis ◽  
Secondary Alcohol ◽  
Allylic Alcohol ◽  
Ring Closing Metathesis ◽  
Relative Configuration ◽  
University Of Utah ◽  
Epothilone B ◽  
Hydride Reduction ◽  
Epothilone A ◽  
The University

The total synthesis of Epothilone B 4, the first natural product (with Epothilone A) to show the same microtubule-stabilizing activity as paclitaxel (Taxol®), has attracted a great deal of attention since that activity was first reported in 1995. The total synthesis of 4 devised (J. Org. Chem. 2008, 73, 9675) by Gary E. Keck of the University of Utah was based in large part on the stereoselective allyl stannane additions (e.g. 1 + 2 → 3 ) that his group originated. The allyl stannane 2 was prepared from the acid chloride 5. Exposure of 5 to Et3N generated the ketene, that was homologated with the phosphorane 6 to give the allene ester 7. Cu-mediated conjugate addition of the stannylmethyl anion 8 then delivered 2. The silyloxy aldehyde 1 was prepared from the ester 9 by reduction with Dibal. Felkincontrolled 1,2-addition of the allyl stannane 2 established the relative configuration of the secondary alcohol of 3, that was then used to control the relative configuration of the new alcohol in 10. Addition of the crotyl borane 12 to the derived aldehyde 11 also proceeded with high diastereocontrol. The other component of 4 was prepared from the aldehyde 14. Enantioselective allylation, by the method the authors developed, delivered the alcohol 16. The Z trisubstituted alkene was then assembled by condensing the aldehyde 17 with the phosphorane 18. Dibal reduction of the product lactone 19 gave a diol, the allylic alcohol of which was selectively converted to the chloride with the Corey-Kim reagent. Hydride reduction then delivered the desired homoallylic alcohol, that was converted to the phosphonium salt 21. Condensation of 21 with 13 gave the diene, that was carried on to Epothilone B 4. The synthesis of Epothilone B 4 as originally conceived by the authors depended on ring-closing metathesis of the triene 22. They prepared 22, but on exposure to the second-generation Grubbs catalyst it was converted only to 23. The authors concluded that the trans acetonide kept 22 in a conformation that did not allow the desired macrocyclization.

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
Keyword(s):  
Total Synthesis ◽  
Epothilone D

The Total Synthesis of Epothilone D as a Yardstick for Probing New Methodologies

2016 ◽  
Vol 23 (3) ◽  
pp. 541-545 ◽  
Author(s):  
Alexander M. Haydl ◽  
Bernhard Breit
Keyword(s):  
Total Synthesis ◽  
Epothilone D ◽  
New Methodologies

scholarly journals Highly Efficient CYP167A1 (EpoK) dependent Epothilone B Formation and Production of 7-Ketone Epothilone D as a New Epothilone Derivative

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Fredy Kern ◽  
Tobias K. F. Dier ◽  
Yogan Khatri ◽  
Kerstin M. Ewen ◽  
Jean-Pierre Jacquot ◽  
...  
Keyword(s):  
Epothilone B ◽  
Highly Efficient ◽  
Epothilone D

Total Synthesis of Oxazole- and Cyclopropane-Containing Epothilone B Analogues by the Macrolactonization Approach

1997 ◽  
Vol 3 (12) ◽  
pp. 1971-1986 ◽  
Author(s):  
K. C. Nicolaou ◽  
Francisco Sarabia ◽  
M. Ray V. Finlay ◽  
Sacha Ninkovic ◽  
N. Paul King ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Epothilone B

scholarly journals Crystal Structures of Epothilone D-bound, Epothilone B-bound, and Substrate-free Forms of Cytochrome P450epoK

2003 ◽  
Vol 278 (45) ◽  
pp. 44886-44893 ◽  
Author(s):  
Shingo Nagano ◽  
Huiying Li ◽  
Hideaki Shimizu ◽  
Clinton Nishida ◽  
Hiroshi Ogura ◽  
...  
Keyword(s):  
Crystal Structures ◽  
Epothilone B ◽  
Epothilone D

ChemInform Abstract: Total Synthesis of (-)-Epothilone B.

ChemInform ◽  
2010 ◽  
Vol 29 (49) ◽  
pp. no-no
Author(s):  
S. A. MAY ◽  
P. A. GRIECO
Keyword(s):  
Total Synthesis ◽  
Epothilone B
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