Iridium-catalyzed reductive allylation of esters
The catalytic reductive transformation of carboxylic esters into α-branched ethers is described. The procedure pivots on the chemoselective iridium-catalyzed hydrosilylation of ester and lactone functionality to afford a silyl acetal intermediate. Upon treatment with a Lewis acid, these hemilabile i...
Main Authors: | Xie, L, Rogers, J, Anastasiou, I, Leitch, J, Dixon, D |
---|---|
Formato: | Journal article |
Idioma: | English |
Publicado em: |
American Chemical Society
2019
|
Registos relacionados
-
Iridium-catalyzed reductive Ugi-type reactions of tertiary amides
Por: Xie, L, et al.
Publicado em: (2018) -
Iridium-catalyzed reductive Ugi-type reactions of tertiary amides
Por: Lan-Gui Xie, et al.
Publicado em: (2018-07-01) -
Iridium-catalyzed reductive nitro-Mannich cyclization.
Por: Gregory, A, et al.
Publicado em: (2015) -
Copper catalyzed asymmetric synthesis of chiral allylic esters.
Por: Geurts, K, et al.
Publicado em: (2006) -
Difluoroalkylation of tertiary amides and lactams by an iridium-catalyzed reductive reformatsky reaction
Por: Biallas, P, et al.
Publicado em: (2022)