Enantioselective Synthesis of Phenyl-ethanolamines Through Application of Chiral Sulfoxide
Author:
Affiliation:
1. a Department of Chemistry , Indian Institute of Technology , Powai, Mumbai, India
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397910902765578
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1. m-Octopamine: Normal Occurrence with p-Octopamine in Mammalian Sympathetic Nerves
2. The preparation and absolute configuration of the optically active forms of the diastereoisomers of 2-(1-phenylethyl)amino-1-phenylethanol and their use as chiral auxiliaries in the asymmetric reduction of acetophenone with modified lithium aluminium hydrides
3. Efficient asymmetric hydrogenation of α-aminoacetophenone derivatives leading to practical synthesis of ()-(−)-levamisole
4. The first enantioselective syntheses of pure R- and S-isoproterenol
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1. Efficient Synthesis of 2‐Amino‐1‐Arylethanols Through a Lewis Base‐Catalyzed SiCl 4 ‐Mediated Asymmetric Passerini‐Type Reaction;European Journal of Organic Chemistry;2020-10-28
2. Prospects for the development of bronchodilators;Russian Chemical Bulletin;2015-09
3. ChemInform Abstract: Enantioselective Synthesis of Phenyl-ethanolamines Through Application of Chiral Sulfoxide.;ChemInform;2010-01-26
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