Asymmetric Synthesis. Part 2.† Enantioselective Conjugate Addition of Grignard Reagents to the Cinnamamide and Crotonamide deriving from (R)-(–)-N-(2-Fluorobenzyl)-2-aminobutanol. Determination of Diastereoisomeric Excess by 19F NMR Spectroscopy
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1997/JC/A704353H
Reference5 articles.
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3. Asymmetric 1,4-addition of organocuprates to chiral .alpha.,.beta.-unsaturated N-acyl-4-phenyl-2-oxazolidinones: a new approach to the synthesis of chiral .beta.-branched carboxylic acids
4. Determination of the enantiomeric excesses of chiral acids by 19F NMR studies of their esters deriving from (R)-(+)-2-(trifluoromethyl)benzhydrol
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1. Conjugate Addition II;Key Chiral Auxiliary Applications;2014
2. ChemInform Abstract: Asymmetric Synthesis. Part 2. Enantioselective Conjugate Addition of Grignard Reagents to the Cinnamamide and Crotonamide Deriving from (R)-(-)-N-(2-Fluorobenzyl)-2-aminobutanol. Determination of Diastereoisomeric Excess by 19F NMR Sp;ChemInform;2010-06-23
3. Catalytic Asymmetric Conjugate Addition and Allylic Alkylation with Grignard Reagents;Chemical Reviews;2008-08-01
4. Synthesis of versatile chiral intermediates by enantioselective conjugate addition of alkenyl Grignard reagents to enamides deriving from (R)-(−)- or (S)-(+)-2-aminobutan-1-ol;Tetrahedron: Asymmetry;1998-05
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