메뉴 건너뛰기




Volumn , Issue 21, 2010, Pages 4088-4097

Aza-Michael addition reactions of hydrazones with activated alkynes catalyzed by nitrogen-containing organic bases

Author keywords

Alkynes; Hydrazones; Michael addition; Organocatalysis

Indexed keywords


EID: 77954709871     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201000365     Document Type: Article
Times cited : (22)

References (70)
  • 1
    • 2842558331 scopus 로고
    • The addition was first discovered by Hantzsch, Komnenos, Crismer and Claisen. Later on, it was summarized by Michael, in 1.887: a) T. Purdie, Ber. Dtsch. Chem. Ges. 1881, 14, 2238-2286;
    • (1881) Ber. Dtsch. Chem. Ges. , vol.14 , pp. 2238-2286
    • Purdie, T.1
  • 8
    • 77954726394 scopus 로고
    • German Patent 2155113
    • The MBH reaction was first reported by Morita in 1.968 and by Baylis and Hillman in 1972: a) A. B. Baylis, M. E. D. Hillman, German Patent 2155113, 1.972;
    • (1972)
    • Baylis, A.B.1    Hillman, M.E.D.2
  • 10
  • 13
    • 0032953281 scopus 로고    scopus 로고
    • For recent accounts of catalytic Michael addition reactions, see: a) I Rodriguez, Synlett 1999, 505-518;
    • (1999) Synlett , pp. 505-518
    • Rodriguez, I.1
  • 16
    • 0037148995 scopus 로고    scopus 로고
    • For recent examples of Michael addition reactions catalyzed by inorganic base: a) S.-M. Ma, S.-H. Yin, L.-T Li, F-G. Tao, Org. Lett. 2002, 4, 505-507;
    • (2002) Org. Lett. , vol.4 , pp. 505-507
    • Ma, S.-M.1    Yin, S.-H.2    Li, L.-T.3    Tao, F.-G.4
  • 18
    • 0037680780 scopus 로고    scopus 로고
    • For Michael addition reactions catalyzed by nucleophilic phosphane Lewis base, see: D. Bhuniya, S. Mohan, S. Narayanan, Synthesis 2003, 1018-1024.
    • (2003) Synthesis , pp. 1018-1024
    • Bhuniya, D.1    Mohan, S.2    Narayanan, S.3
  • 19
    • 0038637120 scopus 로고    scopus 로고
    • Phosphane-catalyzed hydration and hydroalkoxylation of activated olefins have been reported: a) I. C Stewart, R. G. Bergman, F. D. Toste, J. Am. Chem. Soc. 2003, 125, 8696-8697 and references cited therein;
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 8696-8697
    • Stewart, I.C.1    Bergman, R.G.2    Toste, F.D.3
  • 22
    • 70350438872 scopus 로고    scopus 로고
    • for some representative reviews in nitrogen-containing base-catalyzed Michael addition reactions, see: d) A. Alexakis, S. Sulzer-Mossé, Chem. Commun. 2007, 3123-3135;
    • (2007) Chem. Commun. , pp. 3123-3135
    • Alexakis, A.1    Sulzer-Mossé, S.2
  • 26
    • 0842347891 scopus 로고
    • Oxa-Michael addition was first reported by Loydl in 1878: a) F. Loydl, Justus Liebigs Ann. Chem. 1878, 192, 80-89;
    • (1878) Justus Liebigs Ann. Chem. , vol.192 , pp. 80-89
    • Loydl, F.1
  • 27
    • 44349084170 scopus 로고    scopus 로고
    • for some recent reviews on the oxa-Michael reaction, see: b) C. F. Nising, S. Bräse, Chem. Soc. Rev. 2008, 37, 1218-1228 and the references cited therein;
    • (2008) Chem. Soc. Rev. , vol.37 , pp. 1218-1228
    • Nising, C.F.1    Bräse, S.2
  • 28
    • 77954702727 scopus 로고    scopus 로고
    • [6g] and the references cited therein
    • [6g] and the references cited therein.
  • 29
    • 84980076456 scopus 로고
    • Aza-Michael addition was first reported in the reaction of ammonia with, acetone or mesityloxide to form, diacetoneamine in 1.874: a) N. Sokoloff, P. Latschinoff, Ber. Dtsch. Chem. Ges. 1874, 7, 1384-1387;
    • (1874) Ber. Dtsch. Chem. Ges. , vol.7 , pp. 1384-1387
    • Sokoloff, N.1    Latschinoff, P.2
  • 32
    • 70350506798 scopus 로고    scopus 로고
    • for some recent reviews on the azaMichael reaction, see: d) D. Enders, C. Wang, J. X. Liebich, Chem. Eur. J. 2009, 15, 11058-11076 and the references cited therein;
    • (2009) Chem. Eur. J. , vol.15 , pp. 11058-11076
    • Enders, D.1    Wang, C.2    Liebich, J.X.3
  • 33
    • 77954724977 scopus 로고    scopus 로고
    • [6s] and the references cited therein
    • [6s] and the references cited therein.
  • 62
    • 0000140103 scopus 로고    scopus 로고
    • for some recent reviews on the reactions of activated alkynes, see: d) Z.-M. Chen, M. L. Trudell, Chem. Rev. 1996, 96, 1179-1193 and the references cited therein;
    • (1996) Chem. Rev. , vol.96 , pp. 1179-1193
    • Chen, Z.-M.1    Trudell, M.L.2
  • 64
    • 77954739872 scopus 로고    scopus 로고
    • note
    • w 0.0504/0.1328.
  • 65
    • 77954702074 scopus 로고    scopus 로고
    • note
    • w 0.0626/0.1637.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.