A novel C~-symmetric bis-sulfoxide 1 was synthesized as a chiral auxiliary for asymmetric desymmetrization of meso-1,2-diols. cis-Cyclohexane-1,2-dioi and cis-cyclopentane-1,2-diol were desymmetrized via acetalization with I followed by basepromoted acetal cleavage with high diastereoselectivity (>9
Desymmetrization of Meso 1,3- and 1,4-Diols with a Dinuclear Asymmetric Catalyst.
β Scribed by Barry M. Trost; Takashi Mino
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 162 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Desymmetrization reactions of meso compounds through enantioselective catalysis are a powerful strategy for the synthesis of chiral molecules with multiple stereocenters. One well-known example is the Pd-catalyzed desymmetrization of meso-2-alkene-1,4-diol derivatives (Trosts Pd-catalyzed asymmetric
Desymmetrization reactions of meso compounds through enantioselective catalysis are a powerful strategy for the synthesis of chiral molecules with multiple stereocenters. One well-known example is the Pd-catalyzed desymmetrization of meso-2-alkene-1,4-diol derivatives (Trosts Pd-catalyzed asymmetric