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Asymmetric Syntheses of Pharmaceuticals Containing a Cyclopropane Moiety Using Catalytic Asymmetric Simmons-Smith Reactions of Allylalcohols: Syntheses of Optically Active Tranylcypromine and Milnacipran.
- Source :
- Chemistry Letters; 10/5/2013, Vol. 42 Issue 10, p1311-1313, 3p
- Publication Year :
- 2013
-
Abstract
- Asymmetric synthesis of tranylcypromine was achieved using an enantioselective SimmonsSmith cyclopropanation catalyzed by a simple disulfonamide derived from an α-amino acid. The optically active milnacipran was also synthesized by porcine pancreas lipase-catalyzed selective monoacylation of the C4-hydroxy group in (Z)-2-phenylbut-2-ene-1,4-diol and the enantioselective Simmons-Smith cyclopropanation as the key steps. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03667022
- Volume :
- 42
- Issue :
- 10
- Database :
- Supplemental Index
- Journal :
- Chemistry Letters
- Publication Type :
- Academic Journal
- Accession number :
- 120710412
- Full Text :
- https://doi.org/10.1246/cl.130498