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Volumn 53, Issue 10, 2012, Pages 1275-1277

Amine-directed intramolecular hydroacylation of alkenes and alkynes

Author keywords

Heteroatom directed; Intramolecular hydroacylation; Medium ring heterocycles; Rhodium(I) catalyst

Indexed keywords

ALKENE DERIVATIVE; ALKYNE DERIVATIVE; AMINE; RHODIUM;

EID: 84856503810     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.12.125     Document Type: Article
Times cited : (28)

References (40)
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    • For reviews on heteroatom-directed C-H activation, see
    • For reviews on heteroatom-directed C-H activation, see: D.A. Colby, R.G. Bergman, and J.A. Ellman Chem. Rev. 110 2010 624 655
    • (2010) Chem. Rev. , vol.110 , pp. 624-655
    • Colby, D.A.1    Bergman, R.G.2    Ellman, J.A.3
  • 3
    • 77349099246 scopus 로고    scopus 로고
    • For reviews of rhodium-catalyzed hydroacylation, see
    • For reviews of rhodium-catalyzed hydroacylation, see: M.C. Willis Chem. Rev. 110 2010 725 748
    • (2010) Chem. Rev. , vol.110 , pp. 725-748
    • Willis, M.C.1
  • 5
    • 34147095358 scopus 로고    scopus 로고
    • For examples of intermolecular hydroacylation with unfunctionalized aldehydes, see
    • For examples of intermolecular hydroacylation with unfunctionalized aldehydes, see: K. Tanaka, Y. Shibata, T. Suda, Y. Hagiwara, and M. Hirano Org. Lett. 9 2007 1215 1218
    • (2007) Org. Lett. , vol.9 , pp. 1215-1218
    • Tanaka, K.1    Shibata, Y.2    Suda, T.3    Hagiwara, Y.4    Hirano, M.5
  • 7
    • 40549088216 scopus 로고    scopus 로고
    • For examples of hydroacylation with picolyl and quinolyl imines, see
    • For examples of hydroacylation with picolyl and quinolyl imines, see: Y.J. Park, J.-W. Park, and C.-H. Jun Acc. Chem. Res. 41 2008 222 234
    • (2008) Acc. Chem. Res. , vol.41 , pp. 222-234
    • Park, Y.J.1    Park, J.-W.2    Jun, C.-H.3
  • 13
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    • For examples of hydroacylation with β-S-substituted aldehydes, see
    • For examples of hydroacylation with β-S-substituted aldehydes, see: M.C. Willis, S.J. McNally, and P.J. Beswick Angew. Chem., Int. Ed. 43 2004 340 343
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 340-343
    • Willis, M.C.1    McNally, S.J.2    Beswick, P.J.3
  • 40
    • 0001441588 scopus 로고
    • We observed similar results in our earlier work with sulfur substrates. Unsubstituted enones dimerized via a hetero-Diels-Alder pathway. See Ref. 9 and V.J. Traynelis, J.C. Sih, and D.M. Borgnaes J. Org. Chem. 38 1973 2629 2637
    • (1973) J. Org. Chem. , vol.38 , pp. 2629-2637
    • Traynelis, V.J.1    Sih, J.C.2    Borgnaes, D.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.