Synthesis of enantiopure 2-aminoalkylphenols by stereoselective addition of Grignard reagents to chiral 2-imidoylphenols
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference31 articles.
1. Asymmetric synthesis of amines by nucleophilic 1,2-addition of organometallic reagents to the CN-double bond
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3. Addition of Organometallic Reagents to Imines Bearing Stereogenic N-Substituents. Stereochemical Models Explaining the 1,3-Asymmetric Induction
4. Asymmetric Addition of Alkyllithium to Chiral Imines: α-Naphthylethyl Group as a Chiral Auxiliary
5. Asymmetric Addition of Organolithium Reagents to Imines
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1. Convenient Methods for the Synthesis of Chiral Amino Alcohols and Amines;CHIMIA;2013-02-27
2. Stereoselective synthesis of new vicinal diaminoalkyl naphthols by three component Mannich type reaction of α,β-unsaturated aldehydes;Tetrahedron: Asymmetry;2011-07
3. Novel stereoselective synthesis of 2,3-dihydro-1H-benzo[f]chromen-3-amine derivatives through a one-pot three-component reaction;Tetrahedron: Asymmetry;2011-07
4. 2,4-Dichloro-6-((1R)-1-{[(R)-(2-chlorophenyl)(cyclopentyl)methyl]amino}ethyl)phenol;Acta Crystallographica Section E Structure Reports Online;2009-10-17
5. Synthesis of enantiopure 2-(aminoalkyl)phenol derivatives and their application as catalysts in stereoselective reactions;Chirality;2009-01
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