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Volumn 67, Issue 38, 2011, Pages 7263-7267

1,2,3-Triazol-5-ylidene-palladium complex catalyzed Mizoroki-Heck and Sonogashira coupling reactions

Author keywords

1,2,3 Triazole; Catalysis; Cross coupling; N Heterocyclic carbene; Palladium

Indexed keywords

1,2,3 TRIAZOLE DERIVATIVE; ALKENE; ALKYNE; BIS 1,4 DIMESITYL 1,2,3 TRIAZOL 5 YLIDENE PALLADIUM COMPLEX; BROMIDE; CHLORIDE; PALLADIUM COMPLEX; UNCLASSIFIED DRUG;

EID: 80051795332     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.07.045     Document Type: Article
Times cited : (69)

References (44)
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    • For reviews on NHC-Pd-catalyzed cross-coupling reactions, see
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    • 0035959456 scopus 로고    scopus 로고
    • For recent 4 years research on Suzuki-Miyaura cross-coupling reactions, see
    • N.J. Whitcombe, K.K. Hii, and S.E. Gibson Tetrahedron 57 2001 7449 For recent 4 years research on Suzuki-Miyaura cross-coupling reactions, see
    • (2001) Tetrahedron , vol.57 , pp. 7449
    • Whitcombe, N.J.1    Hii, K.K.2    Gibson, S.E.3
  • 17
    • 57549115030 scopus 로고    scopus 로고
    • For recent 4 years research of Mizoroki-Heck reactions cross coupling reactions, see
    • N. Marion, and S.P. Nolan Acc. Chem. Res. 41 2008 1440. For recent 4 years research of Mizoroki-Heck reactions cross coupling reactions, see
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1440
    • Marion, N.1    Nolan, S.P.2
  • 33
    • 80051801728 scopus 로고    scopus 로고
    • For reviews on abnormal NHCs see
    • For reviews on abnormal NHCs see
  • 43
    • 80051795124 scopus 로고    scopus 로고
    • The use of electron-rich aryl iodides instead of bromides gave the quantitative yields of products.
    • The use of electron-rich aryl iodides instead of bromides gave the quantitative yields of products.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.