A superior, readily available enantiopure ligand for the catalytic enantioselective addition of diethylzinc to a-substituted aldehydes

Keyphrases

• Enantiopure Ligand 100%
• High Enantioselectivity 100%
• Enantioselective Addition 100%
• Diethylzinc 100%
• Substituted Aldehydes 100%
• Alcohol 50%
• Room Temperature 50%
• Enantioselectivity 50%
• Oxides 50%
• Aldehydes 50%
• Amino Alcohols 50%
• Regioselectivity 50%
• Stereospecific 50%
• Piperidine 50%
• Ortho 50%
• Enantiomeric Excess 50%
• Benzaldehyde 50%
• Morpholine 50%
• Aliphatic Aldehydes 50%
• Lithium Perchlorate 50%
• Ring Opening 50%
• Secondary Amines 50%
• Aromatic Aldehydes 50%
• Et2Zn 50%
• Triphenylene 50%
• Trifluoromethylphenylpiperazine (TFMPP) 50%
• N-methylpiperazine 50%
• Naphthaldehyde 50%
• Substituted Benzaldehydes 50%

Chemistry

• Enantiopurity 100%
• Enantioselectivity 100%
• Diethylzinc 100%
• Benzaldehyde 66%
• Lithium 33%
• Ring Opening Reaction 33%
• Secondary Amine 33%
• Morpholine 33%
• Piperidine 33%
• N-Methylpiperazine 33%
• Triphenylethylene 33%
• Ambient Reaction Temperature 33%
• Amino Alcohol 33%
• Perchlorate 33%
• Naphthaldehyde 33%
• Enantiomer 33%
• Aldehyde 33%

Pharmacology, Toxicology and Pharmaceutical Science

• Diethylzinc 100%
• Perchlorate 50%
• Alcohol Derivative 50%
• Morpholine 50%
• Benzaldehyde 50%
• Benzaldehyde Derivative 50%
• Aminoalcohol 50%
• Piperidine 50%
• Aldehyde 50%