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Volumn 11, Issue 16, 2009, Pages 3774-3776

Olefinic-amide and olefinic-lactam cyclizations

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; AMIDE; LACTAM;

EID: 68949144472     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901448n     Document Type: Article
Times cited : (10)

References (34)
  • 1
    • 4344610661 scopus 로고    scopus 로고
    • For representative examples of the use of enol ethers in synthesis, see: a
    • For representative examples of the use of enol ethers in synthesis, see: (a) Castro, A. M. M. Chem. Rev. 2004, 104, 2939-3002.
    • (2004) Chem. Rev , vol.104 , pp. 2939-3002
    • Castro, A.M.M.1
  • 3
    • 52149098218 scopus 로고    scopus 로고
    • For representative examples of the use of enamides in synthesis, see: a
    • For representative examples of the use of enamides in synthesis, see: (a) Carbery, D. R. Org. Biomol. Chem. 2008, 6, 3455-3460.
    • (2008) Org. Biomol. Chem , vol.6 , pp. 3455-3460
    • Carbery, D.R.1
  • 10
    • 34247623591 scopus 로고    scopus 로고
    • For reviews on the generation of heterocycles using a combination of metathesis and alkylidenation, see: a
    • For reviews on the generation of heterocycles using a combination of metathesis and alkylidenation, see: (a) Hartley, R. C.; Li, J.; Main, C. A.; McKiernan, G. J. Tetrahedron 2007, 63, 4825-4864.
    • (2007) Tetrahedron , vol.63 , pp. 4825-4864
    • Hartley, R.C.1    Li, J.2    Main, C.A.3    McKiernan, G.J.4
  • 16
    • 0000535557 scopus 로고    scopus 로고
    • For examples of RCM cyclizations of enamides generated using noncarbonyl olefination strategies, see: (a) Kinderman, S. S, van Maarseveen, J. H, Schoemaker, H. E, Hiemstra, H, Rutjes, P. J. T. Org. Lett. 2001, 3, 2045-2048
    • For examples of RCM cyclizations of enamides generated using noncarbonyl olefination strategies, see: (a) Kinderman, S. S.; van Maarseveen, J. H.; Schoemaker, H. E.; Hiemstra, H.; Rutjes, P. J. T. Org. Lett. 2001, 3, 2045-2048.
  • 19
    • 12144288301 scopus 로고    scopus 로고
    • Rosillo, M.; Dominguez, G.; Casarrubios, L.; Amador, U.; Pérez,-Castells, J. J. Org. Chem. 2004, 69, 2084-2093.
    • (d) Rosillo, M.; Dominguez, G.; Casarrubios, L.; Amador, U.; Pérez,-Castells, J. J. Org. Chem. 2004, 69, 2084-2093.
  • 26
    • 0000091226 scopus 로고    scopus 로고
    • In their synthesis of capnellene, the Grubbs group generated a cyclobutene from a related ring-opening metathesis, carbonyl olefination reaction. See: (a) Stille, J. R, Grubbs, R. H. J. Am. Chem. Soc. 1986, 108, 855-856
    • In their synthesis of capnellene, the Grubbs group generated a cyclobutene from a related ring-opening metathesis, carbonyl olefination reaction. See: (a) Stille, J. R.; Grubbs, R. H. J. Am. Chem. Soc. 1986, 108, 855-856.
  • 28
    • 0031166454 scopus 로고    scopus 로고
    • For selected examples of the use of four-membered rings in ring-opening metathesis, see: a
    • For selected examples of the use of four-membered rings in ring-opening metathesis, see: (a) Maughon, B. R.; Grubbs, R. H. Macromolecules 1997, 30, 3459-3469.
    • (1997) Macromolecules , vol.30 , pp. 3459-3469
    • Maughon, B.R.1    Grubbs, R.H.2
  • 33
    • 44949162112 scopus 로고    scopus 로고
    • For related reactions of enamines see
    • For related reactions of enamines see Hurley, P. B.; Dake, G. R. J. Org. Chem. 2008, 73, 4131-4138.
    • (2008) J. Org. Chem , vol.73 , pp. 4131-4138
    • Hurley, P.B.1    Dake, G.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.