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Volumn 17, Issue 24, 1998, Pages 5216-5218

Regio- and diastereoselective nucleophilic additions of lithium enolates on the allenylidene complexes [Ru{=C=C=C(R)Ph}(n5-C9H7)(PPh3) 2][PF6] (R = H, Ph): Synthesis of the first chiral keto-functionalized (σ-Alkynyl)ruthenium(II) complexes

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EID: 0001100052     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om980515n     Document Type: Article
Times cited : (33)

References (5)
  • 1
    • 0000802242 scopus 로고
    • Ruthenium(II) allenylidene complexes have been proposed as key intermediates in the catalytic coupling of 2-propyn-1-ol derivatives with allylic alcohols: (a) Trost, B. M.; Flygare, J. A. J. Am. Chem. Soc. 1992, 114, 5476. (b) Trost, B. M. Chem. Ber. 1996, 129, 1313. Organic cumulenes have been prepared by starting from rhodium(I) allenylidene derivatives: (c) Wiedemann, R.; Steinert, P.; Gevert, O.; Werner, H. J. Am. Chem. Soc. 1996, 118, 2495. (d) Werner, H.; Wiedemann, R.; Mahr, N.; Steinert, P.; Wolf, J. Chem. Eur. J. 1996, 2, 561. (e) Werner, H.; Laubender, M.; Wiedemann, R.; Windmüller, B. Aneew. Chem., Int. Ed. Engl. 1996, 35, 1237.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 5476
    • Trost, B.M.1    Flygare, J.A.2
  • 2
    • 0000293467 scopus 로고    scopus 로고
    • Ruthenium(II) allenylidene complexes have been proposed as key intermediates in the catalytic coupling of 2-propyn-1-ol derivatives with allylic alcohols: (a) Trost, B. M.; Flygare, J. A. J. Am. Chem. Soc. 1992, 114, 5476. (b) Trost, B. M. Chem. Ber. 1996, 129, 1313. Organic cumulenes have been prepared by starting from rhodium(I) allenylidene derivatives: (c) Wiedemann, R.; Steinert, P.; Gevert, O.; Werner, H. J. Am. Chem. Soc. 1996, 118, 2495. (d) Werner, H.; Wiedemann, R.; Mahr, N.; Steinert, P.; Wolf, J. Chem. Eur. J. 1996, 2, 561. (e) Werner, H.; Laubender, M.; Wiedemann, R.; Windmüller, B. Aneew. Chem., Int. Ed. Engl. 1996, 35, 1237.
    • (1996) Chem. Ber. , vol.129 , pp. 1313
    • Trost, B.M.1
  • 3
    • 0029927413 scopus 로고    scopus 로고
    • Ruthenium(II) allenylidene complexes have been proposed as key intermediates in the catalytic coupling of 2-propyn-1-ol derivatives with allylic alcohols: (a) Trost, B. M.; Flygare, J. A. J. Am. Chem. Soc. 1992, 114, 5476. (b) Trost, B. M. Chem. Ber. 1996, 129, 1313. Organic cumulenes have been prepared by starting from rhodium(I) allenylidene derivatives: (c) Wiedemann, R.; Steinert, P.; Gevert, O.; Werner, H. J. Am. Chem. Soc. 1996, 118, 2495. (d) Werner, H.; Wiedemann, R.; Mahr, N.; Steinert, P.; Wolf, J. Chem. Eur. J. 1996, 2, 561. (e) Werner, H.; Laubender, M.; Wiedemann, R.; Windmüller, B. Aneew. Chem., Int. Ed. Engl. 1996, 35, 1237.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 2495
    • Wiedemann, R.1    Steinert, P.2    Gevert, O.3    Werner, H.4
  • 4
    • 0000332488 scopus 로고    scopus 로고
    • Ruthenium(II) allenylidene complexes have been proposed as key intermediates in the catalytic coupling of 2-propyn-1-ol derivatives with allylic alcohols: (a) Trost, B. M.; Flygare, J. A. J. Am. Chem. Soc. 1992, 114, 5476. (b) Trost, B. M. Chem. Ber. 1996, 129, 1313. Organic cumulenes have been prepared by starting from rhodium(I) allenylidene derivatives: (c) Wiedemann, R.; Steinert, P.; Gevert, O.; Werner, H. J. Am. Chem. Soc. 1996, 118, 2495. (d) Werner, H.; Wiedemann, R.; Mahr, N.; Steinert, P.; Wolf, J. Chem. Eur. J. 1996, 2, 561. (e) Werner, H.; Laubender, M.; Wiedemann, R.; Windmüller, B. Aneew. Chem., Int. Ed. Engl. 1996, 35, 1237.
    • (1996) Chem. Eur. J. , vol.2 , pp. 561
    • Werner, H.1    Wiedemann, R.2    Mahr, N.3    Steinert, P.4    Wolf, J.5
  • 5
    • 0029791327 scopus 로고    scopus 로고
    • Ruthenium(II) allenylidene complexes have been proposed as key intermediates in the catalytic coupling of 2-propyn-1-ol derivatives with allylic alcohols: (a) Trost, B. M.; Flygare, J. A. J. Am. Chem. Soc. 1992, 114, 5476. (b) Trost, B. M. Chem. Ber. 1996, 129, 1313. Organic cumulenes have been prepared by starting from rhodium(I) allenylidene derivatives: (c) Wiedemann, R.; Steinert, P.; Gevert, O.; Werner, H. J. Am. Chem. Soc. 1996, 118, 2495. (d) Werner, H.; Wiedemann, R.; Mahr, N.; Steinert, P.; Wolf, J. Chem. Eur. J. 1996, 2, 561. (e) Werner, H.; Laubender, M.; Wiedemann, R.; Windmüller, B. Aneew. Chem., Int. Ed. Engl. 1996, 35, 1237.
    • (1996) Aneew. Chem., Int. Ed. Engl. , vol.35 , pp. 1237
    • Werner, H.1    Laubender, M.2    Wiedemann, R.3    Windmüller, B.4


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