Synthesis of the taxol core via catalytic asymmetric 1,4-addition of an Alkylzirconium Nucleophile
The Taxol core was prepared in five steps via a key copper-catalyzed asymmetric conjugate addition trapping sequence. The use of a bromodiene-derived alkylzirconium nucleophile followed by trapping with POCl3/DMF gave a highly functionalized intermediate featuring a quaternary center in 69% yield wi...
Auteurs principaux: | Wang, JYJ, Fletcher, S |
---|---|
Format: | Journal article |
Langue: | English |
Publié: |
American Chemical Society
2020
|
Documents similaires
-
Copper-catalysed asymmetric 1,4-conjugate addition of alkylzirconium compounds
par: Maksymowicz, R, et autres
Publié: (2012) -
Synthesis of the Taxol core using asymmetric 1,4-additions
par: Wang, JY
Publié: (2020) -
A convenient catalytic asymmetric conjugate addition reaction to enones using alkylzirconium reagents
par: Maksymowicz, R, et autres
Publié: (2013) -
A convenient catalytic asymmetric conjugate addition reaction to enones using alkylzirconium reagents
par: Maksymowicz, R, et autres
Publié: (2013) -
Asymmetric conjugate addition of alkylzirconium reagents to α,β-unsaturated lactones.
par: Maciver, E, et autres
Publié: (2014)