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Volumn 45, Issue 6, 2004, Pages 1137-1141

Synthesis of substituted imidazolines via [3+2]-cycloaddition of aziridines with nitriles

Author keywords

Aziridine; BF3 Et2O; Imidazolines; Triethyloxonium tetrafluoroborate; 3+2 Cycloaddition

Indexed keywords

AZIRIDINE DERIVATIVE; BORIC ACID; IMIDAZOLINE DERIVATIVE; NITRILE; TRIETHYLOXONIUM FLUOROBORATE; UNCLASSIFIED DRUG;

EID: 0742287100     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.12.015     Document Type: Article
Times cited : (55)

References (33)
  • 16
    • 0343484636 scopus 로고
    • Only a few reports are known where harsh conditions and higher amounts of nitrile were used and the examples are limited to only acetonitrile and benzonitrile
    • Only a few reports are known where harsh conditions and higher amounts of nitrile were used and the examples are limited to only acetonitrile and benzonitrile Hiyama T., Koide H., Fujita S., Nozaki H. Tetrahedron. 29:1973;3137.
    • (1973) Tetrahedron , vol.29 , pp. 3137
    • Hiyama, T.1    Koide, H.2    Fujita, S.3    Nozaki, H.4
  • 22
    • 0037124665 scopus 로고    scopus 로고
    • For reaction of activated nitriles with azides, see:
    • For reaction of activated nitriles with azides, see: Demko Z.P., Sharpless K.B. Angew. Chem., Int. Ed. 41:2002;2113.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 2113
    • Demko, Z.P.1    Sharpless, K.B.2
  • 25
    • 85030911766 scopus 로고    scopus 로고
    • note
    • 13C NMR and mass spectrometry, and elemental analysis.
  • 26
    • 85030905326 scopus 로고    scopus 로고
    • note
    • ++1).
  • 28
    • 85030900382 scopus 로고    scopus 로고
    • note
    • Crystallographic data has been deposited with the Cambridge Crystollographic Data Centre as supplementary publication no CCDC-210538. This data can be obtained free of charge via the internet www.ccdc.cam.ac.uk/conts/ retrieving.html or by sending an email to deposit@ccdc.cam.ac.uk.
  • 33
    • 0033588056 scopus 로고    scopus 로고
    • For use of Mg in methanol, see: Ref. 13, and for use of sodium naphthalenide, see:
    • For use of Mg in methanol, see: Ref. 13, and for use of sodium naphthalenide, see: Bergmeier S.C., Seth P.P. Tetrahedron Lett. 40:1999;6181.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 6181
    • Bergmeier, S.C.1    Seth, P.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.