Enantioselective epoxidation of an allylic alcohol catalyzed by (acetylacetonato)-(l-N-methylprolinol)dioxomolybdenum. The decrease of enantioselectivity with chemical conversion-Reference-Cited by-同舟云学术

Enantioselective epoxidation of an allylic alcohol catalyzed by (acetylacetonato)-(l-N-methylprolinol)dioxomolybdenum. The decrease of enantioselectivity with chemical conversion

Published:1983-04 Issue:1 Volume:246 Page:53-56
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Coleman-Kammula S.,Duim-Koolstra E.Th.

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference7 articles.

1. Photochemical Generation of Ru(bpy)3+ and 02 -

2. Chiral hydroxamic acids as ligands in the vanadium catalyzed asymmetric epoxidation of allylic alcohols by tert-butyl hydroperoxide

3. The first practical method for asymmetric epoxidation

4. .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines

5. R.A. Sheldon, Recl. Trav. Chim. Pays-Bas 92 (2973) 253.

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