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Volumn , Issue 32, 2010, Pages 6145-6148

A concise catalytic route to the marine sesquiterpenoids (-)-clavukerin A and (-)-isoclavukerin A

Author keywords

Domino reactions; Metathesis; Michael addition; Organocatalysis; Ruthenium; Terpenoids

Indexed keywords


EID: 78249268215     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001087     Document Type: Article
Times cited : (27)

References (40)
  • 19
    • 73649100972 scopus 로고    scopus 로고
    • Recent review on hydroazulene synthesis:
    • Recent review on hydroazulene synthesis:, D. A. Foley, A. R. Maguire, Tetrahedron 2010, 66, 1131 - 1175.
    • (2010) Tetrahedron , vol.66 , pp. 1131-1175
    • Foley, D.A.1    Maguire, A.R.2
  • 20
    • 78249251850 scopus 로고    scopus 로고
    • Recent reviews
    • Recent reviews
  • 21
    • 77954305294 scopus 로고    scopus 로고
    • M. Mori, Materials 2010, 3, 2087 - 2140.
    • (2010) Materials , vol.3 , pp. 2087-2140
    • Mori, M.1
  • 23
    • 78249262394 scopus 로고    scopus 로고
    • See also
    • See also
  • 28
    • 78249255898 scopus 로고    scopus 로고
    • For Michael addition of 5a and 5b to 7 in the presence of an achiral amine catalyst, see
    • For Michael addition of 5a and 5b to 7 in the presence of an achiral amine catalyst, see
  • 32
    • 78249242837 scopus 로고    scopus 로고
    • Treatment of 10a with methylene(triphenyl)phosphorane (3 equiv.) in benzene at reflux for 3 h yielded 75% 3a next to 7% recovered 10a.
    • Treatment of 10a with methylene(triphenyl)phosphorane (3 equiv.) in benzene at reflux for 3 h yielded 75% 3a next to 7% recovered 10a.
  • 34
    • 84936299305 scopus 로고
    • For generation of halogen-free terminal alkynes as minor products upon treatment of 1,1-dibromoolefins bearing aromatic substituents with methylene(triphenyl)phosphorane (3 equiv.), see:
    • For generation of halogen-free terminal alkynes as minor products upon treatment of 1,1-dibromoolefins bearing aromatic substituents with methylene(triphenyl)phosphorane (3 equiv.), see:, H. J. Bestmann, H. Frey, Liebigs Ann. Chem. 1980, 2061 - 2071.
    • (1980) Liebigs Ann. Chem. , pp. 2061-2071
    • Bestmann, H.J.1    Frey, H.2
  • 37
  • 38
    • 78249232721 scopus 로고    scopus 로고
    • [10,11]
    • [10,11]
  • 40
    • 0012834678 scopus 로고    scopus 로고
    • Preparation according to:, - 4212; Angew. Chem. Int. Ed. 2002, 41, 4038 -4040.
    • Preparation according to:, K. Grela, S. Harutyunyan, A. Michrowska, Angew. Chem. 2002, 114, 4210 - 4212; Angew. Chem. Int. Ed. 2002, 41, 4038 -4040.
    • (2002) Angew. Chem. , vol.114 , pp. 4210
    • Grela, K.1    Harutyunyan, S.2    Michrowska, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.