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Volumn , Issue 8, 1989, Pages 1375-1379

Addition-rearrangement reactions of N-(arylsulphonyloxy)amines and 3,4-dihydro-2H-pyran

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EID: 37049071182     PISSN: 14727781     EISSN: None     Source Type: Journal    
DOI: 10.1039/p19890001375     Document Type: Article
Times cited : (11)

References (37)
  • 19
    • 0000073370 scopus 로고
    • Most electrophilic aminations utilize derivatives of hydroxylamine and give primary amine products. See: (a) Ref. 2
    • R. V. Hoffman and G. A. Buntain, J. Org. Chem., 1988, 53, 3316. Most electrophilic aminations utilize derivatives of hydroxylamine and give primary amine products. See: (a) Ref. 2.
    • (1988) J. Org. Chem , vol.53 , pp. 3316
    • Hoffman, R.V.1    Buntain, G.A.2
  • 20
    • 0003734236 scopus 로고
    • ' ed. S. Patai, Wiley Interscience, London, For other methods of primary electrophilic amination see
    • T. Sheradsky, in 'The Chemistry of Functional Groups, Supplement F, Part 1,' ed. S. Patai, Wiley Interscience, London, 1982, pp. 365-400. For other methods of primary electrophilic amination see
    • (1982) 'The Chemistry of Functional Groups, Supplement F, Part 1 , pp. 365-400
    • Sheradsky, T.1
  • 23
    • 0003571802 scopus 로고
    • For recent attempts to produce more highly substituted amines by electrophilic amination see
    • S. J. Brois, J. Am. Chem. Soc, 1970, 92, 1079. For recent attempts to produce more highly substituted amines by electrophilic amination see
    • (1970) J. Am. Chem. Soc , vol.92 , pp. 1079
    • Brois, S.J.1
  • 29
    • 33845551823 scopus 로고
    • and references therein. G. A. Buntain, unpublished results
    • R. V. Hoffman and G. B. Buntain, J. Org. Chem., 1983,48, 3308 and references therein. G. A. Buntain, unpublished results.
    • (1983) J. Org. Chem , vol.48 , pp. 3308
    • Hoffman, R.V.1    Buntain, G.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.