Conformational control in the SuperQuat chiral auxiliary 5,5-dimethyl-4-iso-propyloxazolidin-2-one induces the iso-propyl group to mimic a tert-butyl group
1H NMR nOe spectroscopic studies reveal that conformational control in the enolates of N-acyl-5,5-dimethyl-4-iso-propyloxazolidin-2-ones ensures that the stereodirecting effect of its 4-iso-propyl-5,5-dimethyl functional group affords superior levels of facial selectivity normally associated with en...
主要な著者: | Bull, S, Davies, S, Key, MS, Nicholson, R, Savory, E |
---|---|
フォーマット: | Journal article |
言語: | English |
出版事項: |
2000
|
類似資料
-
SuperQuat 5,5-dimethyl-4-iso-propyloxazolidin-2-one as a mimic of Evans 4-tert-butyloxazolidin-2-one.
著者:: Bull, S, 等
出版事項: (2006) -
A practical procedure for the multigram synthesis of the SuperQuat chiral auxiliaries
著者:: Bull, S, 等
出版事項: (1998) -
SuperQuat chiral auxiliaries: design, synthesis, and utility
著者:: Davies, SG, 等
出版事項: (2018) -
Asymmetric alkylations using SuperQuat auxiliaries - an investigation into the synthesis and stability of enolates derived from 5,5-disubstituted oxazolidin-2-ones
著者:: Bull, S, 等
出版事項: (1999) -
SuperQuat, (S)-4-benzyl-5,5-dimethyl-oxazolidin-2-one for the asymmetric synthesis of alpha-substituted aldehydes
著者:: Bull, S, 等
出版事項: (2000)