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Volumn , Issue 2, 2012, Pages 251-254

Intramolecular conjugate addition of α,β-unsaturated lactones having an alkanenitrile side chain: Stereocontrolled construction of carbocycles with quaternary carbon atoms

Author keywords

carbocycles; cyclization; Michael addition; nitriles; stereoselective synthesis

Indexed keywords

LACTONE DERIVATIVE; NITRILE; TRIETHYLAMINE; TRIFLUOROMETHANESULFONIC ACID;

EID: 84855845414     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1290074     Document Type: Article
Times cited : (14)

References (11)
  • 1
    • 27544458968 scopus 로고    scopus 로고
    • For representative reviews of the stereoselective construction of all-carbon quaternary stereogenic centers, see:, Christoffers J, Baro A, Adv. Synth. Catal. 2005 347 1473
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 1473
    • Christoffers, J.1    Baro, A.2
  • 8
    • 0036135888 scopus 로고    scopus 로고
    • The intramolecular alkylation reactions of nitriles provide useful carbocyclization method. For an excellent review of nitrile anion cyclization, see:, Fleming F F., Shook B C., Tetrahedron 2002 58 1
    • (2002) Tetrahedron , vol.58 , pp. 1
    • Fleming, F.F.1    Shook, B.C.2
  • 11
    • 77953907329 scopus 로고    scopus 로고
    • note
    • aC NMR spectroscopy. In this context, Denmark and Wilson have recently reported the Lewis base catalyzed intermolecular conjugate addition of silyl ketene imines to,-unsaturated carbonyl compounds, see:, Denmark S E., Wilson T W., Synlett 2010 1723
    • (2010) Synlett , pp. 1723
    • Denmark, S.E.1    Wilson, T.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.