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Volumn 30, Issue 11, 2011, Pages 2920-2932

Hybrid thiophosphoryl-benzothiazole palladium SCN-pincer complexes: Synthesis and effect of structure modifications on catalytic performance in the suzuki cross-coupling

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVE COMPLEXES; ARYL BROMIDES; BENZOTHIAZOLES; CATALYTIC PERFORMANCE; CHLOROACETOPHENONE; CYCLOPALLADATION; HIGH YIELD; PHENYLBORONIC ACIDS; PINCER COMPLEXES; PINCER-TYPE LIGAND; STRUCTURE MODIFICATION; SUZUKI CROSS COUPLING;

EID: 79958178455     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om101012r     Document Type: Article
Times cited : (53)

References (91)
  • 1
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    • For reviews on the Suzuki-Miyaura cross-coupling, see
    • For reviews on the Suzuki-Miyaura cross-coupling, see: Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457.
    • (1995) Chem. Rev. , vol.95 , pp. 2457
    • Miyaura, N.1    Suzuki, A.2
  • 12
    • 41849117318 scopus 로고    scopus 로고
    • For some recent advances in application of Suzuki crosscoupling, see
    • For some recent advances in application of Suzuki crosscoupling, see: Molander, G. A.; Gormisky, P. E.; Sandrock, D. L. J. Org. Chem. 2008, 73, 2052.
    • (2008) J. Org. Chem. , vol.73 , pp. 2052
    • Molander, G.A.1    Gormisky, P.E.2    Sandrock, D.L.3
  • 34
    • 0035886138 scopus 로고    scopus 로고
    • For reviews on catalytic properties of pincer complexes, see
    • For reviews on catalytic properties of pincer complexes, see: (a) Albrecht, M.; van Koten, G. Angew. Chem., Int. Ed. 2001, 40, 3750.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 3750
    • Albrecht, M.1    Van Koten, G.2
  • 43
    • 66549104202 scopus 로고    scopus 로고
    • For recent examples of application of pincer complexes for the Suzuki-Miyaura cross-coupling, see
    • For recent examples of application of pincer complexes for the Suzuki-Miyaura cross-coupling, see: Zhang, B.-Sh.; Wang, Ch.; Gong, J.-F.; Song, M.-P. J. Organomet. Chem. 2009, 694, 2555.
    • (2009) J. Organomet. Chem. , vol.694 , pp. 2555
    • Zhang, B.-S.1    Wang, C.2    Gong, J.-F.3    Song, M.-P.4
  • 69
    • 79958089059 scopus 로고    scopus 로고
    • In the Suzuki reaction usually no side products are observed. Indeed, in the reactions catalyzed by complexes 12-15, no products of homocoupling were detected at any significant level according to theGC data, so conversion of the starting aryl halide was perceived to conform with the yield of a biphenyl product
    • In the Suzuki reaction usually no side products are observed. Indeed, in the reactions catalyzed by complexes 12-15, no products of homocoupling were detected at any significant level according to theGC data, so conversion of the starting aryl halide was perceived to conform with the yield of a biphenyl product.
  • 70
    • 79958104763 scopus 로고    scopus 로고
    • Such a pathway of (pre)catalyst decomposition was previously observed for another type of pincer palladacycle having a coordinated O-P=S moiety, that is, thiophosphoryloxy-thiophosphoryl palladium pincer complexes X
    • Such a pathway of (pre)catalyst decomposition was previously observed for another type of pincer palladacycle having a coordinated O-P=S moiety, that is, thiophosphoryloxy-thiophosphoryl palladium pincer complexes X.
  • 85
    • 79958180306 scopus 로고    scopus 로고
    • 12
    • 12


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.