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Volumn 9, Issue 9, 2007, Pages 1749-1752

Ruthenium-catalyzed tandem cross-metathesis/wittig olefination: Generation of conjugated dienoic esters from terminal olefins

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; ESTER; RUTHENIUM;

EID: 34248331775     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol070445t     Document Type: Article
Times cited : (54)

References (82)
  • 1
    • 17844369291 scopus 로고    scopus 로고
    • For select reviews on olefin metathesis, see: a, Murahashi, S.-I, Ed, Wiley-VCH: Weinheim, Chapter 6
    • For select reviews on olefin metathesis, see: (a) Grubbs, R. H.; Trnka, T. M. In Ruthenium in Organic Synthesis; Murahashi, S.-I., Ed.; Wiley-VCH: Weinheim, 2004; Chapter 6.
    • (2004) Ruthenium in Organic Synthesis
    • Grubbs, R.H.1    Trnka, T.M.2
  • 6
    • 1442360753 scopus 로고    scopus 로고
    • Grubbs, R. H, Ed, Wiley-VCH: Weinheim, Germany
    • (a) Handbook of Metathesis; Grubbs, R. H., Ed.; Wiley-VCH: Weinheim, Germany, 2003.
    • (2003) Handbook of Metathesis
  • 11
    • 33644529063 scopus 로고    scopus 로고
    • For examples of olefin metatheses in target-oriented syntheses from our laboratory, see: (a) Shizuka, M, Schrader, T. O, Snapper, M. L. J. Org. Chem. 2006, 71, 1330
    • For examples of olefin metatheses in target-oriented syntheses from our laboratory, see: (a) Shizuka, M.; Schrader, T. O.; Snapper, M. L. J. Org. Chem. 2006, 71, 1330.
  • 36
    • 27744499721 scopus 로고    scopus 로고
    • For examples of tandem reaction sequences with ruthenium metathesis catalysts developed outside of our laboratory, see: (a) Schmidt, B, Pohler, M. J. Organomet. Chem. 2005, 690, 5552
    • For examples of tandem reaction sequences with ruthenium metathesis catalysts developed outside of our laboratory, see: (a) Schmidt, B.; Pohler, M. J. Organomet. Chem. 2005, 690, 5552.
  • 65
    • 0003966689 scopus 로고
    • Sporn, M. B, Roberts, A. B, Goodman, D. S, Eds, Academic Press: NY, Vols
    • (c) The Retinoids; Sporn, M. B., Roberts, A. B., Goodman, D. S., Eds.; Academic Press: NY, 1984; Vols. 1-2.
    • (1984) The Retinoids , vol.1-2
  • 75
    • 33751216844 scopus 로고    scopus 로고
    • Ferrie, L.; Amans, D.; Reymond, S.; Bellosta, V.; Capdevielle, P.; Cossy, J. J. Organomet. Chem. 2006, 691, 5456. For a recent review of ene-diene cross metathesis, see:
    • (f) Ferrie, L.; Amans, D.; Reymond, S.; Bellosta, V.; Capdevielle, P.; Cossy, J. J. Organomet. Chem. 2006, 691, 5456. For a recent review of ene-diene cross metathesis, see:
  • 79
    • 0034685462 scopus 로고    scopus 로고
    • Although all ruthenium complexes (I-IV) effected the Wittig olefination, the catalyst selected for the tandem process was dictated by reactivity in the CM and relative cost. Chatterjee, A. K, Morgan, J. P, Scholl, M, Grubbs, R. H. J. Am. Chem. Soc. 2000, 122, 3783
    • Although all ruthenium complexes (I-IV) effected the Wittig olefination, the catalyst selected for the tandem process was dictated by reactivity in the CM and relative cost. Chatterjee, A. K.; Morgan, J. P.; Scholl, M.; Grubbs, R. H. J. Am. Chem. Soc. 2000, 122, 3783.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.