ChemInform Abstract: Enzyme-Catalyzed Reactions. Part 26. Stereoselective Synthesis of (1R)- and (1R,2S)-1-Aryl-2-alkylamino Alcohols from (R)-Cyanohydrins.
β Scribed by F. EFFENBERGER; B. GUTTERER; J. JAEGER
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 30 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Enzyme-Catalyzed Reactions. Part 26. Stereoselective Synthesis of (1R)-and (1R,2S)-1-Aryl-2-alkylamino Alcohols from (R)-Cyanohydrins.
-Enantiomerically pure N-alkylated amino alcohols are prepared from cyanohydrins, accessible by (R)-oxynitrilase catalyzed addition of HCN to the appropriate aldehydes as previously reported. The title compounds are sympathomimetics of pharmacological interest. -(EFFENBERGER, F.;
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v