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Volumn 16, Issue 2, 2014, Pages 386-389

Iron-catalyzed reductive cyclization of 1,6-enynes

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EID: 84896740693     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol403257x     Document Type: Article
Times cited : (32)

References (49)
  • 13
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    • Shen, H. C. Tetrahedron 2008, 64, 7847-7870.
    • (2008) Tetrahedron , vol.64 , pp. 7847-7870
    • Shen, H.1
  • 15
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    • For some examples
    • For some examples: (h) Park, J. H.; Kim, S. M.; Chung, Y. K. Chem.-Eur. J. 2011, 17, 10852-10856
    • (2011) Chem.-Eur. J. , vol.17 , pp. 10852-10856
    • Park, J.1    Kim, S.2    Chung, Y.3
  • 32
    • 58149156301 scopus 로고    scopus 로고
    • For related reports of iron-catalyzed reductive cyclization of activated 1,6-enynes
    • For related reports of iron-catalyzed reductive cyclization of activated 1,6-enynes: (a) Hata, T.; Hirone, N.; Sujaku, S.; Nakano, K.; Urabe, H. Org. Lett. 2008, 10, 5031-5033
    • (2008) Org. Lett. , vol.10 , pp. 5031-5033
    • Hata, T.1    Hirone, N.2    Sujaku, S.3    Nakano, K.4    Urabe, H.5
  • 34
    • 0034671743 scopus 로고    scopus 로고
    • For Studies Of The So-called "inorganic Grignard reagent"by reaction of FeX2 and RMgX, see
    • For studies of the so-called "inorganic Grignard reagent" by reaction of FeX2 and RMgX, see: (a) Bogdanovic, B.; Schwickardi, M. Angew. Chem., Int. Ed. 2000, 39, 4610-4612
    • (2000) Angew. Chem., Int. Ed. , Issue.39 , pp. 4610-4612
    • Bogdanovic, B.1    Schwickardi, M.2
  • 41
    • 0032577046 scopus 로고    scopus 로고
    • Formation of material of high polarity which we tentatively attributed to polymerization of the substrate was also observed under the reaction conditions. For iron-catalyzed polymerization of olefins
    • Formation of material of high polarity, which we tentatively attributed to polymerization of the substrate, was also observed under the reaction conditions. For iron-catalyzed polymerization of olefins, see: (a) Small, B. L; Brookhart, M.; Bennett, A. M. A. J. Am. Chem. Soc. 1998, 120, 4049-4050
    • (1998) J. Am. Chem. Soc. , Issue.120 , pp. 4049-4050
    • Small, B.L.1    Brookhart, M.2    Bennett, A.A.M.3
  • 44
    • 84896779740 scopus 로고    scopus 로고
    • We thank an anonymous reviewer for suggesting the experiment with 2e
    • We thank an anonymous reviewer for suggesting the experiment with 2e.
  • 48
    • 53549097924 scopus 로고    scopus 로고
    • For a similar mechanistic hypothesis of a nickel-catalyzed reductive cyclization of 1,6-enynes
    • For a similar mechanistic hypothesis of a nickel-catalyzed reductive cyclization of 1,6-enynes, see: Chen, M.; Weng, Y.; Guo, M.; Zhang, H.; Lei, A. Angew. Chem., Int. Ed. 2008, 47, 2279-2282.
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 2279-2282
    • Chen, M.1    Weng, Y.2    Guo, M.3    Zhang, H.4    Lei, A.5
  • 49
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    • The following aldehydes (3 equiv) were used as the electrophile: 4-trifluoromethylbenzaldehyde, 4-methoxybenzaldehyde, and hydrocinnamaldehyde
    • The following aldehydes (3 equiv) were used as the electrophile: 4-trifluoromethylbenzaldehyde, 4-methoxybenzaldehyde, and hydrocinnamaldehyde.


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