Enzymatic resolution of methyl 2-alkyl-2-arylacetates
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (50) , 7053-7056
- https://doi.org/10.1016/s0040-4039(01)93421-5
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- .alpha.-Amino acids as chiral educts for asymmetric products. Alkylation of N-phenylfluorenyl .alpha.-amino ketones. Synthesis of optically pure .alpha.-alkyl carboxylic acidsJournal of the American Chemical Society, 1988
- A facile and efficient preparative method of methyl 2-arylpropanoates by treatment of propiophenones and their derivatives with iodine or iodine chloridesThe Journal of Organic Chemistry, 1988
- Asymmetric hydroformylation catalyzed by homogeneous and polymer-supported platinum complexes containing chiral phosphine ligandsJournal of the American Chemical Society, 1987
- Tartaric acid, an efficient chiral auxiliary: new asymmetric synthesis of 2-alkyl-2-arylacetic acidsThe Journal of Organic Chemistry, 1987
- A General Synthetic Method of Chiral 2-Arylalkanoic Esters via Thermal 1,2-RearrangementBulletin of the Chemical Society of Japan, 1987
- Tetrahedron report number 205Tetrahedron, 1986
- A facile enzymatic resolution process for the preparation of (+)--2-(6-hethoxy-2-naphthyl)propionic acid (Naproxen).Tetrahedron Letters, 1986
- Stereoselective Inversion of (R)-Fenoprofen to (S)-Fenoprofen in HumansJournal of Pharmaceutical Sciences, 1985
- OPTICALLY ACTIVE NAPROXEN BY KINETIC RESOLUTIONChemistry Letters, 1984
- Nonsteroidal antiinflammatory agents. I. 6-Substituted 2-naphthylacetic acidsJournal of Medicinal Chemistry, 1970