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Volumn 47, Issue 7, 2008, Pages 1176-1178

The catalytic asymmetric strecker reaction: Ketimines continue to join the fold

Author keywords

Asymmetric synthesis; Cyanides; Homogeneous catalysis; Ketimines; Strecker reaction

Indexed keywords

AMINATION; AMINO ACIDS; CYANIDES; ORGANIC ACIDS;

EID: 41249092756     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200703879     Document Type: Review
Times cited : (131)

References (39)
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    • Shibasaki and co-workers also demonstrated that the use of stoichiometric HCN in conjunction with catalytic amounts of TMSCN resulted in highly effective catalysis: N. Kato, M. Suzuki, M. Kanai, M. Shibasaki, Tetrahedron Lett. 2004, 45, 3153
    • Shibasaki and co-workers also demonstrated that the use of stoichiometric HCN in conjunction with catalytic amounts of TMSCN resulted in highly effective catalysis: N. Kato, M. Suzuki, M. Kanai, M. Shibasaki, Tetrahedron Lett. 2004, 45, 3153.
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    • Catalyst 13a did not catalyze the addition of HCN itself to imine substrates.
    • Catalyst 13a did not catalyze the addition of HCN itself to imine substrates.
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    • A referee has pointed out that in the presence of stoichiometric amounts of isopropyl alcohol, an analogous catalysis mode involving the activation of HCN by the quinuclidine ring nitrogen could also be considered. For a discussion of the influence of protic additives see
    • A referee has pointed out that in the presence of stoichiometric amounts of isopropyl alcohol, an analogous catalysis mode involving the activation of HCN by the quinuclidine ring nitrogen could also be considered. For a discussion of the influence of protic additives see: M. Takamura, Y. Hamashima, H. Usuda, M. Kanai, M. Shibasaki, Angew. Chem. 2000, 112, 1716;
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.