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Volumn , Issue 28, 2006, Pages 2977-2979

New directions for the Morita-Baylis-Hillman reaction; homologous aldol adducts via epoxide opening

Author keywords

[No Author keywords available]

Indexed keywords

EPOXIDE; PHOSPHINE DERIVATIVE;

EID: 33745813926     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b603510h     Document Type: Article
Times cited : (46)

References (23)
  • 4
    • 0342419508 scopus 로고    scopus 로고
    • For examples of phosphine catalyzed reactions of enones, i.e., an intramolecular vinylogous MBH or an intramolecular Rauhut-Currier reaction, see:
    • D. Basavaiah P. D. Rao R. S. Hyma Tetrahedron 1996 52 8001
    • (1996) Tetrahedron , vol.52 , pp. 8001
    • Basavaiah, D.1    Rao, P.D.2    Hyma, R.S.3
  • 8
    • 22944474675 scopus 로고    scopus 로고
    • For examples of organomediated MBH reactions of allylic carbonates under Pd catalysis, see:
    • M. E. Krafft T. F. N. Haxell J. Am. Chem. Soc. 2005 127 10168
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 10168
    • Krafft, M.E.1    Haxell, T.F.N.2
  • 11
  • 22
    • 0038369752 scopus 로고    scopus 로고
    • Other enones were prepared in a similar manner; see ESI for details
    • R.-H. Fan X.-L. Hou Tetrahedron Lett. 2003 44 4411
    • (2003) Tetrahedron Lett. , vol.44 , pp. 4411
    • Fan, R.-H.1    Hou, X.-L.2
  • 23
    • 33745833770 scopus 로고    scopus 로고
    • Intermolecular enone head-to-tail coupling products, as mixtures of dimers and perhaps trimers, appear to constitute a portion of the remaining material
    • Intermolecular enone head-to-tail coupling products, as mixtures of dimers and perhaps trimers, appear to constitute a portion of the remaining material


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.