Asymmetric aldol addition reactions of a chiral 3-sulfonyl-1,3-oxazolidine-masked lithium 2-formylcyclohexanone enolate
β Scribed by Inga Hoppe; Dieter Hoppe; Regine Herbst-Irmer; Ernst Egert
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 171 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
The origin of virtually complete face diastereoselectivity in the organic base-catalyzed, room temperature Michael addition reactions between Ni(II)-complexes of Schiff bases of glycine and chiral 3-(Eenoyl)-4-substituted-1,3-oxazolidin-2-ones was shown to stem from the unusual mode of steric intera
## A stoicbiometric Itmomtofthccbiral~1turntdouttos tlaxssivcly promote the aqmmehic aldol rcactioa of al&hy&s with cd silyl ethers and the rdowitlg asymmettic leductioa in om pot to affcrd syI&l3diols willlbighetity.
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