Asymmetric remote C-H functionalization: use of internal olefins in tandem hydrometallation-isomerization-asymmetric conjugate addition sequences
We describe catalytic asymmetric C-C formation using terminal alkyl-metal nucleophiles generated from internal olefins through a 'chain-walking' isomerization mechanism. Hydrometallation of internal olefins with the Schwartz reagent gives the least hindered alkyl-zirconocene after thermal...
Hlavní autoři: | Mola, L, Sidera, M, Fletcher, S |
---|---|
Médium: | Journal article |
Vydáno: |
CSIRO Publishing
2015
|
Podobné jednotky
-
Asymmetric remote C-H functionalization: Use of internal olefins in tandem hydrometallation – isomerization – asymmetric conjugate addition sequences
Autor: Mola, L, a další
Vydáno: (2014) -
Hydrometallation-asymmetric conjugate addition: application to complex molecule synthesis.
Autor: Maksymowicz, R, a další
Vydáno: (2013) -
Formation of quaternary centers by copper-catalyzed asymmetric conjugate addition of alkylzirconium reagents.
Autor: Sidera, M, a další
Vydáno: (2013) -
A convenient catalytic asymmetric conjugate addition reaction to enones using alkylzirconium reagents
Autor: Maksymowicz, R, a další
Vydáno: (2013) -
A convenient catalytic asymmetric conjugate addition reaction to enones using alkylzirconium reagents
Autor: Maksymowicz, R, a další
Vydáno: (2013)