Understanding the origins of remote asymmetric induction in the boron aldol reactions of beta-alkoxy methyl ketones.
We report theoretical studies into the remote 1,5-stereoinduction shown by certain types of beta-alkoxy methyl ketones in boron-mediated aldol reactions with achiral aldehydes. For a range of common alkoxy groups, our calculations are in excellent agreement with experimentally observed diastereosele...
Автори: | Paton, R, Goodman, J |
---|---|
Формат: | Journal article |
Мова: | English |
Опубліковано: |
2006
|
Схожі ресурси
Схожі ресурси
-
1,5-anti stereocontrol in the boron-mediated aldol reactions of beta-alkoxy methyl ketones: the role of the formyl hydrogen bond.
за авторством: Paton, R, та інші
Опубліковано: (2008) -
Enantioselectivity in the boron aldol reactions of methyl ketones.
за авторством: Goodman, J, та інші
Опубліковано: (2007) -
Alkylation and aldol reactions of acyl derivatives of N-1-(1 '-naphthyl)ethyl-O-tert-butylhydroxylamine: asymmetric synthesis of alpha-alkoxy-, alpha-substituted-beta-alkoxy- and alpha,beta-dialkoxyaldehydes
за авторством: Chernega, A, та інші
Опубліковано: (2010) -
Indução assimétrica 1,5-Anti na adição de enolatos de boro de metilcetonas beta-oxigenadas a aldeídos 1,5-Asymmetric induction in the boron-mediated aldol reaction of beta-oxygenated methyl ketones
за авторством: Luiz C. Dias, та інші
Опубліковано: (2007-01-01) -
Asymmetric cross-aldol reaction of isatin and ketones catalyzed by crude earthworm extract as efficient biocatalyst
за авторством: Fatemeh Shams, та інші
Опубліковано: (2020-07-01)