trans-2-Phenoxycyclohexan-1-OL as New Chiral Auxiliary: Synthesis of Chiral α-Hydroxy Acids
- 1 March 1992
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 22 (6) , 941-947
- https://doi.org/10.1080/00397919208020858
Abstract
(1R,2R)-2-Phenoxycyclohexan-1-ol is used as a chiral auxiliary for the preparation of α-hydroxy acids in high optical purities.Keywords
This publication has 13 references indexed in Scilit:
- Enantioselective synthesis of α- and β-hydroxy acids using -2-phenylcyclohexan-1-ol-as chiral auxiliaryTetrahedron Letters, 1991
- Convenient enantioselective hydrolysis of racemicTetrahedron Letters, 1990
- Chiral acrylates as substrates in baylis-hillman reactionTetrahedron Letters, 1990
- Towards Chiral Reformatsky ReagentsSynthetic Communications, 1989
- Total synthesis of (-)-SpecioninJournal of the American Chemical Society, 1988
- Enantioselective ring construction through asymmetric olefin-ketene cycloaddition. A highly enantiocontrolled approach to (-)-.alpha.-cuparenone and (+)-.beta.-cuparenoneJournal of the American Chemical Society, 1987
- Camphor derivatives as chiral auxiliaries in asymmetric synthesisTetrahedron, 1987
- Recent advances in asymmetric synthesis-IITetrahedron, 1986
- trans-2-Phenylcyclohexanol. A powerful and readily available chiral auxiliaryThe Journal of Organic Chemistry, 1985
- Preparation of an optically active prostaglandin intermediate via asymmetric inductionJournal of the American Chemical Society, 1975