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Total synthesis of 26-hydroxyepothilone B and related analogues
Home
Publications
Total synthesis of 26-hydroxyepothilone B and related analogues
Total synthesis of 26-hydroxyepothilone B and related analogues
KN
K. C. Nicolaou
K. C. Nicolaou
SN
Sacha Ninkovic
Sacha Ninkovic
MF
M. Ray V. Finlay
M. Ray V. Finlay
FS
Francisco Sarabia
Francisco Sarabia
TL
Tianhu Li
Tianhu Li
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1 January 1997
journal article
research article
Published by
Royal Society of Chemistry (RSC)
in
Chemical Communications
No. 24
,
p.
2343-2344
https://doi.org/10.1039/a705845d
Abstract
A series of 26-substituted epothilones B (3, 22, 23a–n and 24a–h,j–l,o) have been constructed by total synthesis involving a selective Wittig olefination, an aldol reaction and a macrolactonization as key steps.
Keywords
HYDROXYEPOTHILONE
23A
MACROLACTONIZATION
24A
OLEFINATION
EPOTHILONES
SUBSTITUTED
STEPS
ANALOGUES
WITTIG
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Cited by 25 articles