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Volumn 56, Issue 27, 2000, Pages 4765-4768

Synergistic effect in bimetallic Ni-Al clusters. Application to efficient catalytic reductive dehalogenation of polychlorinated arenes

Author keywords

Bimetallic clusters; Nickel catalyst; Reductive dehalogenation

Indexed keywords

POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

EID: 0034733715     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00383-5     Document Type: Article
Times cited : (48)

References (24)
  • 1
    • 0000273466 scopus 로고
    • (a) Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford
    • (a) Hudlicky, M. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 8, p 895.
    • (1991) In Comprehensive Organic Synthesis , vol.8 , pp. 895
    • Hudlicky, M.1
  • 4
    • 0032526306 scopus 로고    scopus 로고
    • and references therein
    • Wei, B.; Hor, T. S. A. J. Mol. Catal. A 1998, 132, 223 and references therein.
    • (1998) J. Mol. Catal. a , vol.132 , pp. 223
    • Wei, B.1    Hor, T.S.A.2
  • 9
    • 0032079603 scopus 로고    scopus 로고
    • (a) and references therein
    • (a) Sarma, K. D.; Maitra, U. Tetrahedron 1998, 54, 4965 and references therein.
    • (1998) Tetrahedron , vol.54 , pp. 4965
    • Sarma, K.D.1    Maitra, U.2
  • 20
    • 0009127081 scopus 로고
    • Previous catalytic use of NaH containing Ni reducing agents (called NiCRA) were briefly described. Note that the results presented in this paper for the Ni-catalysed reactions were obtained under the same conditions as those used for Ni-Al ones
    • Previous catalytic use of NaH containing Ni reducing agents (called NiCRA) were briefly described: Vanderesse, R.; Brunet, J. J.; Caubere, P. J. Org. Chem. 1981, 46, 1270. Note that the results presented in this paper for the Ni-catalysed reactions were obtained under the same conditions as those used for Ni-Al ones.
    • (1981) J. Org. Chem. , vol.46 , pp. 1270
    • Vanderesse, R.1    Brunet, J.J.2    Caubere, P.3
  • 22
    • 85037965098 scopus 로고    scopus 로고
    • Control experiments performed with 1-decene showed that a mixture of various decenes (resulting from double bond isomerisation) was produced besides 5-10% of decane after 18 h
    • Control experiments performed with 1-decene showed that a mixture of various decenes (resulting from double bond isomerisation) was produced besides 5-10% of decane after 18 h.
  • 23
    • 85037952593 scopus 로고    scopus 로고
    • For dehalogenation of polychlorobenzenes, see Refs. 2,4b,4d,7a,8
    • For dehalogenation of polychlorobenzenes, see Refs. 2,4b,4d,7a,8.
  • 24
    • 85037956313 scopus 로고    scopus 로고
    • For dehalogenation of chlorobiphenyls, see Refs. 4a,4c,6a
    • For dehalogenation of chlorobiphenyls, see Refs. 4a,4c,6a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.