Synthesis of β-amino phosphonates in one-pot procedure

Synthetic Communications

Volumn 27, Issue 23, 1997, Pages 4101-4105

  Jang, Won Bum ^a   Shin, Won Suk ^a   Lee, Kilsung ^a   Oh, Dong Young ^a  

^a Korea Advanced Institute of Science and Technology (KAIST)   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINOETHYLPHOSPHONIC ACID; PHOSPHONIC ACID DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; IN VITRO STUDY; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REACTION ANALYSIS;

EID: 0030693679     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919708005457     Document Type: Article

References (16)

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15. In the case of reducing the aromatic nitrile with DIBAL-H or catalytic hydrogenation, benzylidenebenzylamine was produced as a minor product (Benzaldehyde was produced as a major product.): (a) A. E. G. Miller, J. W. Biss, L. H. Schwartzman, J. Org. Chem., 1959, 24, 627. (b) R. Juday, H. Adkins, J. Am. Chem. Soc., 1955, 77, 4559.
16. In the case of reducing the aromatic nitrile with DIBAL-H or catalytic hydrogenation, benzylidenebenzylamine was produced as a minor product (Benzaldehyde was produced as a major product.): (a) A. E. G. Miller, J. W. Biss, L. H. Schwartzman, J. Org. Chem., 1959, 24, 627. (b) R. Juday, H. Adkins, J. Am. Chem. Soc., 1955, 77, 4559.