An efficient synthesis of (R)-(+)- and (S)-(-)-propranolol from resolved 5-idomethyloxazo-lidin-2-ones
- 1 January 1987
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 43 (11) , 2505-2512
- https://doi.org/10.1016/s0040-4020(01)81657-4
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Diastereoselective synthesis of chiral secondary amines with two chiral centers directly attached to the nitrogen atomThe Journal of Organic Chemistry, 1986
- On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcoholsThe Journal of Organic Chemistry, 1986
- Oxazolidin-2-ones from allylic amines by means of iodine and carbonate anion on polymeric support. A convenient synthesis of (.+-.)-propranololThe Journal of Organic Chemistry, 1986
- Investigation of new chiral 1,3-oxazolidine-2-thiones: analytical separation and optical resolution of racemic carboxylic acids and amino acidsJournal of the Chemical Society, Perkin Transactions 1, 1985
- A novel synthesis of methyl .alpha.-L-garosaminide which illustrates a stereocontrolled approach to the cis-hydroxyamino moiety of amino sugarsJournal of the American Chemical Society, 1980
- The Synthesis of Optically-active Valine by the Stereoselective Decarboxylation of α-(α-Methylbenzylamino)-α-isopropylmalonic AcidBulletin of the Chemical Society of Japan, 1973
- Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) estersJournal of the American Chemical Society, 1973
- Optical Isomers of PropranololNature, 1966
- Azomethine Chemistry. I. Formation of Optically Active α-Amino Acids by Asymmetric Induction1Journal of the American Chemical Society, 1961
- A Sterically Controlled Synthesis of Amino AcidsJournal of the American Chemical Society, 1961