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Volumn 4, Issue 8, 2002, Pages 1319-1322

Transition Metal Salts-Catalyzed Aza-Michael Reactions of Enones with Carbamates

Author keywords

[No Author keywords available]

Indexed keywords

CARBAMIC ACID DERIVATIVE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; INORGANIC SALT; METAL;

EID: 0037129388     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0256163     Document Type: Article
Times cited : (195)

References (46)
  • 7
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    • Trost, B. M., Fleming, I., Eds.; Pergamon; Oxford
    • (g) Kleinman, E. F. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon; Oxford, 1991; Vol. 2, p 893.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 893
    • Kleinman, E.F.1
  • 9
    • 0038359012 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, and references therein
    • (i) Jung, M. E. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 4, pp 30-41 and references therein.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 30-41
    • Jung, M.E.1
  • 10
    • 0000862669 scopus 로고    scopus 로고
    • and references therein
    • (j) Kobayashi, S.; Ishitani, H. Chem. Rev. 1999, 99, 1069 and references therein.
    • (1999) Chem. Rev. , vol.99 , pp. 1069
    • Kobayashi, S.1    Ishitani, H.2
  • 23
    • 0034612973 scopus 로고    scopus 로고
    • A review for enantioselective conjugate additions, see: Sibi, M. P.; Manyem, S. Tetrahedron 2000, 56, 8033.
    • (2000) Tetrahedron , vol.56 , pp. 8033
    • Sibi, M.P.1    Manyem, S.2
  • 29
    • 85004504175 scopus 로고
    • intramolecular
    • For base catalysts, see: (a) Hirama, M. J. Synth. Org. Chem., Jpn. 1987, 45, 346 (intramolecular).
    • (1987) J. Synth. Org. Chem., Jpn. , vol.45 , pp. 346
    • Hirama, M.1
  • 35
    • 0034681803 scopus 로고    scopus 로고
    • intramolecular
    • For acid catalyst, see: (f) Takeuchi, Y.; Tokuda, S.; Takagi, T.; Koike, M.; Abe, H.; Harayama, T.; Shibata, Y.; Kim, H.-s.; Wataya, Y. Heterocycles 1999, 51, 1869 (intramolecular). (g) McAlpine, I. J.; Armstrong, R. W. Tetrahedron Lett. 2000, 41, 1849 (intramolecular).
    • (2000) Tetrahedron Lett. , vol.41 , pp. 1849
    • McAlpine, I.J.1    Armstrong, R.W.2
  • 37
    • 33751155795 scopus 로고
    • For recent examples utilizing Pr(IV), Au(III), or Ru(III) chloride as a catalyst for cyclizations of unsaturated compounds or a Friedel - Crafts acylation, see: (a) Blum, J.; Beer-Kraft, H.; Badrieh, Y. J. Org. Chem. 1995, 60, 5567.
    • (1995) J. Org. Chem. , vol.60 , pp. 5567
    • Blum, J.1    Beer-Kraft, H.2    Badrieh, Y.3
  • 44
    • 0442266002 scopus 로고    scopus 로고
    • note
    • 4, filtered, and evaporated. The crude product was purified by preparative TLC to give a β-amino ketone.
  • 45
    • 0442266005 scopus 로고    scopus 로고
    • note
    • 2 as a catalyst; see ref 13.
  • 46
    • 0442264423 scopus 로고    scopus 로고
    • note
    • 3 (a 1: 1 mixture): δ 198.1, 158.4, 137.1, 136.3, 131.8, 130.1, 127.8. 122.4, 19.9.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.