Synthesis of optically active 4-hydroxymandelic acid and derivatives via Regio- and Stereoselective Friedel-Crafts alkylation.
- 31 December 1993
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 4 (12) , 2411-2414
- https://doi.org/10.1016/s0957-4166(00)82212-0
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Synthesis of a Chiral α-(Aminooxy)arylacetic Ester. II. A Route through a Chiral 2-Hydroxy-2-phenylacetic Acid DerivativeBulletin of the Chemical Society of Japan, 1991
- Synthesis of a Chiral α-(Aminooxy)arylacetic Ester. I. A Route through Optical Resolution of a Racemic α-(Phthalimidooxy)arylacetic AcidBulletin of the Chemical Society of Japan, 1990
- Novel sponge-derived amino acids. 11. The entire absolute stereochemistry of the bengamidesThe Journal of Organic Chemistry, 1990
- Highly regio- and diastereoselective Friedel-Crafts alkylation of phenols. Synthesis of 2-hydroxymandelic esters.Tetrahedron: Asymmetry, 1990
- Enantioselective synthesis of optically pure s-isoserineTetrahedron Letters, 1988
- Asymmetric induction in the ene reaction of glyoxylate esters of 8-phenylmentholTetrahedron, 1986
- Selective deprotection of alcoholic and phenolic silyl ethersTetrahedron Letters, 1985
- New perspectives in asymmetric inductionAccounts of Chemical Research, 1985
- Template catalysis via non-transition metal complexes. New highly selective syntheses on phenol systemsPure and Applied Chemistry, 1983
- Studies directed toward the synthesis of prostaglandins. Useful boron-mediated olefin synthesesThe Journal of Organic Chemistry, 1976