Diastereoface differentiating peracid oxidation of the enol ether derived from cyclohexanone and 2,4-pentanediol: Preparation of optically pure 2-hydroxycyclohexanone acetal
- 1 January 1993
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 4 (1) , 43-44
- https://doi.org/10.1016/s0957-4166(00)86013-9
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Asymmetric functionalization of conformationally distinctive Cs-symmetric cis-[n.3.1] bicyclic ketones. Definition of the absolute course of enantio- and diastereodifferentiationThe Journal of Organic Chemistry, 1992
- Chemistry of oxaziridines. 15. Asymmetric oxidations using 3-substituted 1,2-benzisothiazole 1,1-dioxide oxidesThe Journal of Organic Chemistry, 1991
- Enantioselective synthesis of tertiary .alpha.-hydroxy carbonyl compounds using [(8,8-dichlorocamphoryl)sulfonyl]oxaziridineThe Journal of Organic Chemistry, 1990
- Diastereo-differentiating cyclopropanation of a chiral enol ether: a simple method for the preparation of optically pure cyclopropyl ethersTetrahedron, 1990
- Diastereo-differentiating simmons-smith reaction using 2,4-pentanediol as a chiral auxiliaryTetrahedron Letters, 1988
- New methods and reagents in organic synthesis. 75. asymmetric synthesis of α-hydroxy ketones using chiral phase transfer catalystsTetrahedron Letters, 1988
- Preparation of optically active 1,2-diols and .alpha.-hydroxy ketones using glycerol dehydrogenase as catalyst. Limits to enzyme-catalyzed synthesis due to noncompetitive and mixed inhibition by productThe Journal of Organic Chemistry, 1986
- Epoxyethers. IV. Mechanism of the Opening of an Epoxyether with an Organic Acid1Journal of the American Chemical Society, 1953