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Volumn 10, Issue 3, 2008, Pages 405-408

Allylic alkylation and ring-closing metathesis in sequence: A successful cohabitation of Pd and Ru

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EID: 38949103684     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702694v     Document Type: Article
Times cited : (48)

References (34)
  • 3
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    • (a) Tietze, L. F. Chem. Rev. 1996, 96, 115-136.
    • (1996) Chem. Rev , vol.96 , pp. 115-136
    • Tietze, L.F.1
  • 7
    • 0035974362 scopus 로고    scopus 로고
    • For examples of PDOM type I, see: (a) Poli, G, Giambastiani, G, Pacini, B. Tetrahedron Lett. 2001, 42, 5179-5182
    • For examples of PDOM type I, see: (a) Poli, G.; Giambastiani, G.; Pacini, B. Tetrahedron Lett. 2001, 42, 5179-5182.
  • 16
    • 0345868445 scopus 로고    scopus 로고
    • For a selection of significant contributions to this field see: a
    • For a selection of significant contributions to this field see: (a) Lebel, H.; Paquet, V. J. Am. Chem. Soc. 2004, 126, 1152-1153.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 1152-1153
    • Lebel, H.1    Paquet, V.2
  • 24
    • 38949155846 scopus 로고    scopus 로고
    • This process has also been alternatively described as concurrent tandem catalysis (ref 6a, tandem orthogonal catalysis (ref 6b, or cooperative sequential multicatalysis ref 6c
    • This process has also been alternatively described as concurrent tandem catalysis (ref 6a), tandem orthogonal catalysis (ref 6b), or cooperative sequential multicatalysis (ref 6c).
  • 25
    • 0037569997 scopus 로고    scopus 로고
    • The Tsuji-Trost reaction and related carbon-carbon formation reaction
    • Negishi, E.-I, Ed, John Wiley & Sons: NY
    • (a) Tsuji, J. The Tsuji-Trost reaction and related carbon-carbon formation reaction. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E.-I., Ed.; John Wiley & Sons: NY, 2002; pp 16691844.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , pp. 16691844
    • Tsuji, J.1
  • 27
    • 1442360753 scopus 로고    scopus 로고
    • Grubbs, R. H, Ed, John Wiley & Sons: New York
    • Handbook of Metathesis; Grubbs, R. H., Ed.; John Wiley & Sons: New York, 2003.
    • (2003) Handbook of Metathesis
  • 28
    • 0035972021 scopus 로고    scopus 로고
    • 3, and 5 mol % of Grubbs' catalyst second generation or Hoveyda-Grubbs' catalyst. These conditions allow a limited (57%) conversion of the tandem isomerization/RCM. See: (a) Braddock, D. C.; Wildsmith, A. J. Tetrahedron Lett. 2001, 42, 3239- 3242.
    • 3, and 5 mol % of Grubbs' catalyst second generation or Hoveyda-Grubbs' catalyst. These conditions allow a limited (57%) conversion of the tandem isomerization/RCM. See: (a) Braddock, D. C.; Wildsmith, A. J. Tetrahedron Lett. 2001, 42, 3239- 3242.
  • 30
    • 35248813310 scopus 로고    scopus 로고
    • A reverse one-pot sequence, Ru-catalyzed cross metathesis/Pd-catalyzed allylic carbonate reduction has been recently reported by Comins et al. In this sequence, the second catalytic system is added after completion of the first step, yielding a product in 65-85% yield. Comins, D. L.; Dinsmore, J. M.; Marks, L. R. Chem. Commun. 2007, 4170-4171.
    • A reverse one-pot sequence, Ru-catalyzed cross metathesis/Pd-catalyzed allylic carbonate reduction has been recently reported by Comins et al. In this sequence, the second catalytic system is added after completion of the first step, yielding a product in 65-85% yield. Comins, D. L.; Dinsmore, J. M.; Marks, L. R. Chem. Commun. 2007, 4170-4171.
  • 34
    • 0035385137 scopus 로고    scopus 로고
    • Ruthenium-catalyzed allylic alkylation is a well-known process see
    • Ruthenium-catalyzed allylic alkylation is a well-known process see: Trost, B. M.; Toste, F. D.; Pinkerton, A. B. Chem. Rev. 2001, 101, 2067-2096.
    • (2001) Chem. Rev , vol.101 , pp. 2067-2096
    • Trost, B.M.1    Toste, F.D.2    Pinkerton, A.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.