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Volumn 10, Issue 2, 2006, Pages 165-183

Bis(allyl)-ruthenium(IV) complexes: Promising precursors for catalytic organic synthesis

Author keywords

Acetonitrile; Butadiene; Cyclopentadiene; Mononuclear neutral complexes; Polymerization

Indexed keywords

CHLORINE COMPOUNDS; RUTHENIUM COMPOUNDS;

EID: 31944452612     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527206775192933     Document Type: Review
Times cited : (44)

References (107)
  • 1
    • 17844369291 scopus 로고    scopus 로고
    • Murahashi, S.-I., Ed.; Wiley-VCH: Weinheim
    • See for example: (a) Ruthenium in Organic Synthesis; Murahashi, S.-I., Ed.; Wiley-VCH: Weinheim, 2004.
    • (2004) Ruthenium in Organic Synthesis
  • 2
    • 15744379429 scopus 로고    scopus 로고
    • Bruneau, C., Dixneuf, P. H., Eds.; Springer: Berlin
    • (b) Ruthenium Catalysts and Fine Chemistry; Bruneau, C., Dixneuf, P. H., Eds.; Springer: Berlin, 2004.
    • (2004) Ruthenium Catalysts and Fine Chemistry
  • 6
    • 0001603937 scopus 로고
    • Abel, E. W.; Stone, F. G. A.; Wilkinson, G.; Eds.; Pergamon Press: Oxford
    • See for example: (a) Hill, A. F. In Comprehensive Organometallic Chemistry II; Abel, E. W.; Stone, F. G. A.; Wilkinson, G.; Eds.; Pergamon Press: Oxford, 1995; Vol. 7, pp. 299.
    • (1995) Comprehensive Organometallic Chemistry II , vol.7 , pp. 299
    • Hill, A.F.1
  • 7
    • 0346296141 scopus 로고
    • Abel, E. W.; Stone, F. G. A.; Wilkinson, G., Eds.; Pergamon Press: Oxford
    • (b) Bennett, M. A. In Comprehensive Organometallic Chemistry II; Abel, E. W.; Stone, F. G. A.; Wilkinson, G., Eds.; Pergamon Press: Oxford, 1995; Vol. 7, pp. 441.
    • (1995) Comprehensive Organometallic Chemistry II , vol.7 , pp. 441
    • Bennett, M.A.1
  • 8
    • 0001650185 scopus 로고
    • Abel, E. W.; Stone, F. G. A.; Wilkinson, G., Eds.; Pergamon Press: Oxford
    • (c) Bennett, M. A.; Khan, K.; Wenger, E. In Comprehensive Organometallic Chemistry II; Abel, E. W.; Stone, F. G. A.; Wilkinson, G., Eds.; Pergamon Press: Oxford, 1995; Vol. 7, pp. 473.
    • (1995) Comprehensive Organometallic Chemistry II , vol.7 , pp. 473
    • Bennett, M.A.1    Khan, K.2    Wenger, E.3
  • 19
    • 0000951659 scopus 로고
    • Abel, E. W.; Stone, F. G. A.; Wilkinson, G., Eds.; Pergamon Press: Oxford
    • (b) Bennett, M. A. In Comprehensive Organometallic Chemistry II; Abel, E. W.; Stone, F. G. A.; Wilkinson, G., Eds.; Pergamon Press: Oxford, 1995; Vol. 7, pp. 549.
    • (1995) Comprehensive Organometallic Chemistry II , vol.7 , pp. 549
    • Bennett, M.A.1
  • 69
    • 0842327412 scopus 로고    scopus 로고
    • The application of high oxidation state organometallics in aqueous catalysis has been recently highlighted and references therein
    • The application of high oxidation state organometallics in aqueous catalysis has been recently highlighted. Poli, R. Chem. Eur. J., 2004, 10, 332 and references therein.
    • (2004) Chem. Eur. J. , vol.10 , pp. 332
    • Poli, R.1
  • 72
    • 85197363404 scopus 로고    scopus 로고
    • 2] has been obtained by reacting 1 with 2,2′-bipyridine in refluxing acetonitrile: IUC9900125
    • 2] has been obtained by reacting 1 with 2,2′-bipyridine in refluxing acetonitrile: Hub, S.; Park, S.; Lough, A. J. Acta Cryst. Sect. C, 1999, 55, IUC9900125.
    • (1999) Acta Cryst. Sect. C. , vol.55
    • Hub, S.1    Park, S.2    Lough, A.J.3
  • 98
    • 0037239704 scopus 로고    scopus 로고
    • Reviews on catalytic isomerization of allylic alcohols
    • Reviews on catalytic isomerization of allylic alcohols: (a) Uma, R.; Crévisy, C.; Grée R. Chem. Rev., 2003, 103, 27.
    • (2003) Chem. Rev. , vol.103 , pp. 27
    • Uma, R.1    Crévisy, C.2    Grée, R.3
  • 101
    • 0027225733 scopus 로고
    • The use of a base as co-catalyst in allylic alcohols isomerization is well documented. The presence of base favours the chelate coordination of the corresponding allylic alkoxide to the metal, representing the initial step in the catalytic cycle
    • The use of a base as co-catalyst in allylic alcohols isomerization is well documented. The presence of base favours the chelate coordination of the corresponding allylic alkoxide to the metal, representing the initial step in the catalytic cycle. See for example: (a) Bäckvall, J.-E.; Andreasson, U. Tetrahedron Lett., 1993, 34, 5459.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 5459
    • Bäckvall, J.-E.1    Andreasson, U.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.