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Volumn 2, Issue 7, 2000, Pages 949-952

A new route to cyclopentenones via ruthenium-catalyzed carbonylative cyclization of allylic carbonates with alkenes

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EID: 0000498888     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0000206     Document Type: Article
Times cited : (27)

References (52)
  • 1
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    • and pertinent references therein
    • Ellison, R. A. Synthesis 1973, 397 and pertinent references therein.
    • (1973) Synthesis , pp. 397
    • Ellison, R.A.1
  • 8
    • 0001334715 scopus 로고
    • Trost, B. M., Ed.; Pergamon: Oxford, U.K.
    • (g) Schore, N. E. In Comprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon: Oxford, U.K., 1991; Vol. 5, pp 1037-1064
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 1037-1064
    • Schore, N.E.1
  • 9
    • 0001136410 scopus 로고
    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, U.K.
    • (h) Schore, N. E. In Comprehensive Organometallic Chemistry II; Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, U.K., 1995-Vol. 12, pp 703-739.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 703-739
    • Schore, N.E.1
  • 10
    • 0000213863 scopus 로고    scopus 로고
    • Beller, M., BoIm, C., Eds.; Wiley-VCH: New York
    • (I) Jeong, N. In Transition Metals for Organic Synthesis; Beller, M., BoIm, C., Eds.; Wiley-VCH: New York, 1998; Vol. 1, pp 560-577.
    • (1998) Transition Metals for Organic Synthesis , vol.1 , pp. 560-577
    • Jeong, N.1
  • 26
    • 0000147038 scopus 로고
    • and references therein
    • (a) Chiusoli, G. P. Acc. Chem. Res. 1973, 6, 422 and references therein.
    • (1973) Acc. Chem. Res. , vol.6 , pp. 422
    • Chiusoli, G.P.1
  • 41
    • 0001411025 scopus 로고
    • (a) Palladium-catalyzed cyclocarbonylation of allylic halides with 2-norbomene and/or 2,5-norbornadiene to 2-alkylidenecyclopentanones, not cyclopentenones, has been reported, see: Amari, E.; Catellani, M.; Chiusoli, G. P. J. Organomet. Chem. 1985, 285, 383.
    • (1985) J. Organomet. Chem. , vol.285 , pp. 383
    • Amari, E.1    Catellani, M.2    Chiusoli, G.P.3
  • 45
    • 85037493424 scopus 로고    scopus 로고
    • note
    • 3N was used in the following reactions.
  • 46
    • 85037498810 scopus 로고    scopus 로고
    • note
    • 11 which would be obtained by β-hydride elimination prior to CO insertion.
  • 48
    • 85037499502 scopus 로고    scopus 로고
    • note
    • w = 0.070, GOF= 1.12.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.