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Volumn , Issue 4, 2000, Pages 611-616

Addition of Grignard reagents to chiral 1,2-bisimines: A diasteroselective preparation of unsymmetrical 1,2-diamines

Author keywords

(E) 2 NonenalAsymmetric synthesis; 2,3 Benzotropolone; 2H Furo 3,2 b benzopyran 2 ones; Chiral bisimines; Dynamic kinetic resolution; Grignard reactions; Toadstools; Tricholoma; Unsymmetrical 1,2 diamines

Indexed keywords

1,2 DI(TERT BUTYLETHANE)DIAMINE; ANILINE DERIVATIVE; DIAMINE DERIVATIVE; ETHYLAMINE; GLYOXAL; IMINE; MAGNESIUM CHLORIDE; PROPYLAMINE; SOLVENT; UNCLASSIFIED DRUG;

EID: 0034048824     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-0690(200002)2000:4<611::AID-EJOC611>3.0.CO;2-9     Document Type: Article
Times cited : (49)

References (12)
  • 10
    • 0038106171 scopus 로고    scopus 로고
    • and references herein
    • For the addition of organometallic reagents to C = N bonds, see: R. Bloch, Chem. Rev. 1998, 98, 1407-1438 and references herein.
    • (1998) Chem. Rev. , vol.98 , pp. 1407-1438
    • Bloch, R.1
  • 11
    • 85197331533 scopus 로고    scopus 로고
    • note
    • 1H NMR spectroscopy of the crude reaction mixtures as the two diastereomers of the imines 5, 10 and 11 were not separable by chromatography on silica gel.
  • 12
    • 85197335443 scopus 로고    scopus 로고
    • note
    • Crystallographic data (excluding structure factors) for the structure of 15 have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-117666. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [Fax: (internat.) + 44-1223/336-033; E-mail: deposit@jccdc.cam.ac.uk].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.