Asymmetric Epoxidation of Functionalized cis-Olefins Catalyzed by Chloroperoxidase. -Chloroperoxidase in a buffered solution efficiently catalyzes the asymmetric epoxidation of functionalized cis-olefins (7 examples), using tert-butyl hydroperoxide as the terminal reagent. -(HU, SHANGHUI;
Asymmetric epoxidation of functionalized cis-olefins catalyzed by chloroperoxidase
โ Scribed by Shanghui Hu; Lowell P. Hager
- Book ID
- 104260854
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 206 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Chloroperoxidase catalyzes the asymmetric epoxidation of functionalized cis-2-alkenes with excellent enantioselectivity and good yields, using tert-butyl hydroperoxide as the terminal oxidant.
๐ SIMILAR VOLUMES
Chiral ketones 1 and 2 bearing 1-aza-7-oxabicyclo[3.5.0]decane skeleton and their C 2 -symmetric analogue 3 were readily prepared and evaluated as a chiral dioxirane precursor for asymmetric epoxidation of olefins with Oxone ยฎ . The ketone 2, bearing a diphenyl steric wall, was not effective and gav
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