Synthesis of a scalemic β-amino disulfide from (S)-phenylglycine and (R)-styrene oxide and use as a catalyst in enantioselective additions of diethylzinc to aldehydes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. On the way to chiral copper(I) arenethiolate catalysts for the enantioselective conjugate addition of methyl lithium and methyl magnesium iodide to benzylideneacetone
2. Chiral mercaptoaryl-oxazolines as ligands in enantioselective copper-catalyzed 1,4-additions of Grignard reagents to enones
3. Enantioselective Copper-Catalyzed 1,4-Addition ofGrignard Reagents to ?,?-Unsaturated Carbonyl Compounds
4. Catalytic enantioselective conjugate additions using enantiopure β-amino disulfides and β-amino thiolates
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1. Comprehensive quantum chemical and spectroscopic (FTIR, FT-Raman, 1H, 13C NMR) investigations of (1,2-epoxyethyl)benzene and (1,2-epoxy-2-phenyl)propane;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2015-01
2. Modular Prolinol Chiral Ligands for Enantioselective Addition of Diethylzinc to Aromatic Aldehydes;Synthetic Communications;2013-01-07
3. Tandem base-free synthesis of β-hydroxy sulphides under ultrasound irradiation;Journal of Chemical Sciences;2012-09
4. Modular amino acid amide chiral ligands for enantioselective addition of diethylzinc to aromatic aldehydes;Applied Organometallic Chemistry;2011-04-28
5. Recent developments in the asymmetric hydrolytic ring opening of epoxides catalysed by microbial epoxide hydrolase;Tetrahedron: Asymmetry;2010-12
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