A Scaleable Route to the Pure Enantiomers of Verapamil
- 19 August 2000
- journal article
- review article
- Published by American Chemical Society (ACS) in Organic Process Research & Development
- Vol. 4 (6) , 467-472
- https://doi.org/10.1021/op000059q
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Convenient synthesis of (2R)- and (2S)-2-(1-methylethyl)-5-oxo-2-phenylpentanenitrile, intermediates in the preparation of phenylalkylamine calcium channel blockersJournal of the Chemical Society, Perkin Transactions 1, 1996
- 3,4,5-Trifluorobenzeneboronic Acid as an Extremely Active Amidation CatalystThe Journal of Organic Chemistry, 1996
- Human multi‐drug‐resistant cancer cells exhibit a high degree of selectivity for stereoisomers of verapamil and quinidineInternational Journal of Cancer, 1990
- Antimigraine drug interactions with serotonin receptor subtypes in human brainAnnals of Neurology, 1988
- Stereospecific synthesis of the enantiomers of verapamil and gallopamilThe Journal of Organic Chemistry, 1987
- A quantitative approach to optical resolutionTetrahedron Letters, 1980
- Synthèse et configuration absolue des énantiomères du Vér apamilHelvetica Chimica Acta, 1975