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Volumn 46, Issue 47, 2007, Pages 9002-9005

Efficient chirality switching in the addition of diethylzinc to aldehydes in the presence of simple chiral α-amino amides

Author keywords

Amino acids; Asymmetric catalysis; Chirality; Homogeneous catalysis; Ligand design

Indexed keywords

ALCOHOLS; ALDEHYDES; AMINO ACIDS; DERIVATIVES; LIGANDS; METAL COMPLEXES; STOICHIOMETRY;

EID: 36849031953     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200702259     Document Type: Article
Times cited : (50)

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    • Homochiral 1:2 complexes seem to predominate in solution. Thus, no differences could be observed by NMR spectroscopy for complexes formed from enantiomerically pure 1c (R or S) or the racemic mixture. This finding agrees with theoretical calculations RB3LYP/LACVP* level
    • Homochiral 1:2 complexes seem to predominate in solution. Thus, no differences could be observed by NMR spectroscopy for complexes formed from enantiomerically pure 1c (R or S) or the racemic mixture. This finding agrees with theoretical calculations (RB3LYP/LACVP* level).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.