The use of chiral selenium electrophile 6 generated in situ atoms can be generated selectively with diastereoselectivities up to 85% when geminal disubstituted alkenes from the chiral diselenide 5 in asymmetric ring closure reactions of unsaturated alcohols, carboxylic acids and are used. The cycliz
β¦ LIBER β¦
ChemInform Abstract: Chiral Diselenides in Asymmetric Cyclization Reactions.
β Scribed by G. FRAGALE; T. WIRTH
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 35 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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