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Volumn 80, Issue 1, 2015, Pages 690-697

Catalytic C-H Allylation and Benzylation of Pyrazoles

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EID: 84937965737     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo5025317     Document Type: Article
Times cited : (37)

References (70)
  • 1
    • 84879499655 scopus 로고    scopus 로고
    • Katritzky, A. R. Ramsden, C. A. Scriven, E. F. V. Taylor, R. J. K., Eds., Elsevier: Oxford, U.K.
    • Yet. L. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Ramsden, C. A., Scriven, E. F. V., Taylor, R. J. K., Eds.; Elsevier: Oxford, U.K., 2008; Vol. 4, pp 1-141.
    • (2008) Comprehensive Heterocyclic Chemistry , vol.4 , pp. 1-141
    • Yet, L.1
  • 38
    • 79952611097 scopus 로고    scopus 로고
    • For an example of direct allylation and benzylation of oxazoles and thiazoles using N -tosylhydrazones, see: Zhao, X.; Wu, G.; Zhang, Y.; Wang, J. J. Am. Chem. Soc. 2011, 133, 3296
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 3296
    • Zhao, X.1    Wu, G.2    Zhang, Y.3    Wang, J.4
  • 55
    • 84868679055 scopus 로고    scopus 로고
    • The reaction with allyl chloride provided the allylation product 8 in 40% yield along with the olefin isomerization product in 10% yield when PPh3 was absent. The inhibitory effect of the phosphine ligand in the allylation of polyfluoroarenes with allyl chlorides has been noted. Yu, Y.-B.; Fan, S.; Zhang, X. Chem.-Eur. J. 2012, 18, 14643
    • (2012) Chem. - Eur. J. , vol.18 , pp. 14643
    • Yu, Y.-B.1    Fan, S.2    Zhang, X.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.