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Volumn 70, Issue 8, 2005, Pages 3296-3298

Aziridines versus vinyl carbamates from the direct amination of electron-withdrawing group-substituted trifluoromethyl enoates

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; AMINATION; ELECTRON TRANSITIONS; OLEFINS; SOLVENTS; SUBSTITUTION REACTIONS; VINYL RESINS;

EID: 17444396338     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050044w     Document Type: Article
Times cited : (39)

References (44)
  • 1
  • 4
    • 0001834676 scopus 로고    scopus 로고
    • (b) Fluoroorganic Chemistry. Synthetic Challenge and Biomedicinal Rewards; Resnati, G., Soloshonok, V. A., Eds.; Tetrahedron Symposia in Print No. 58; Tetrahedron 1996, 52, 1-330.
    • (1996) Tetrahedron , vol.52 , pp. 1-330
  • 16
    • 0036064894 scopus 로고    scopus 로고
    • For some recent examples, see: (a) Stevens, C. V.; Van Heecke, G.; Barbero, C.; Patora, K.; De Kimpe, N.; Verhe, R. Synlett 2002, 1089-1092. (b) Kozhushkov, S. I.; Leonov, A.; de Meijere, A. Synthesis 2003, 956-958. (c) Matsumoto, T.; Masu, H.; Yamaguchi, K.; Takeda, K. Org. Lett. 2004, 6, 4367-4369 and refs therein.
    • (2002) Synlett , pp. 1089-1092
    • Stevens, C.V.1    Van Heecke, G.2    Barbero, C.3    Patora, K.4    De Kimpe, N.5    Verhe, R.6
  • 17
    • 0038367671 scopus 로고    scopus 로고
    • For some recent examples, see: (a) Stevens, C. V.; Van Heecke, G.; Barbero, C.; Patora, K.; De Kimpe, N.; Verhe, R. Synlett 2002, 1089-1092. (b) Kozhushkov, S. I.; Leonov, A.; de Meijere, A. Synthesis 2003, 956-958. (c) Matsumoto, T.; Masu, H.; Yamaguchi, K.; Takeda, K. Org. Lett. 2004, 6, 4367-4369 and refs therein.
    • (2003) Synthesis , pp. 956-958
    • Kozhushkov, S.I.1    Leonov, A.2    De Meijere, A.3
  • 18
    • 9444224978 scopus 로고    scopus 로고
    • and refs therein
    • For some recent examples, see: (a) Stevens, C. V.; Van Heecke, G.; Barbero, C.; Patora, K.; De Kimpe, N.; Verhe, R. Synlett 2002, 1089-1092. (b) Kozhushkov, S. I.; Leonov, A.; de Meijere, A. Synthesis 2003, 956-958. (c) Matsumoto, T.; Masu, H.; Yamaguchi, K.; Takeda, K. Org. Lett. 2004, 6, 4367-4369 and refs therein.
    • (2004) Org. Lett. , vol.6 , pp. 4367-4369
    • Matsumoto, T.1    Masu, H.2    Yamaguchi, K.3    Takeda, K.4
  • 29
    • 17444377618 scopus 로고
    • Eur. Pat. Appl. EP396364, 1990
    • (a) Bambury, R. E.; Seelye, D. E. Eur. Pat. Appl. EP396364, 1990; Chem. Abstr. 1991, 114, 254062.
    • (1991) Chem. Abstr. , vol.114 , pp. 254062
    • Bambury, R.E.1    Seelye, D.E.2
  • 30
    • 17444379423 scopus 로고
    • US5233077, 1993
    • (b) Waller, F. J. US5233077, 1993; Chem. Abstr. 1994, 120, 9128.
    • (1994) Chem. Abstr. , vol.120 , pp. 9128
    • Waller, F.J.1
  • 35
    • 0013586607 scopus 로고
    • It is reported that aza-Michael-type addition reactions of free sulfinimines toward electrophilic alkenes give both amino alkenes and aziridines; the latter are converted to amino alkenes at room temperature: Furukawa, N.; Oae, S. Synthesis 1975, 30-32.
    • (1975) Synthesis , pp. 30-32
    • Furukawa, N.1    Oae, S.2
  • 39
    • 17444379775 scopus 로고
    • Lwowski, W., Ed.; J. Wiley & Sons: New York, Chapter 6
    • Lwowski, W. In Nitrenes; Lwowski, W., Ed.; J. Wiley & Sons: New York, 1970; Chapter 6.
    • (1970) Nitrenes
    • Lwowski, W.1
  • 40
    • 17444367410 scopus 로고    scopus 로고
    • note
    • 2 are known as the usual conditions for electrophilic amination; see ref 11a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.