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Volumn 78, Issue 16, 2013, Pages 8105-8116

Experimental and theoretical studies of selective thiol-ene and thiol-yne click reactions involving N -substituted maleimides

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ADDITION REACTIONS;

EID: 84962382578     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo4014436     Document Type: Article
Times cited : (53)

References (66)
  • 35
    • 47549097918 scopus 로고    scopus 로고
    • It should be noted that bis-maleimides have been used for sequential thiol-Michael click reactions before; however, sequential reactivity was achieved by using excess bis-maleimide rather than inherently selective thiol-ene reactions, see: Li, M.; De, P.; Gondi, S. R.; Sumerlin, B. S. J. Polym. Sci., Part A: Polym. Chem. 2008, 46, 5093
    • (2008) J. Polym. Sci., Part A: Polym. Chem. , vol.46 , pp. 5093
    • Li, M.1    De, P.2    Gondi, S.R.3    Sumerlin, B.S.4
  • 41
    • 84865437158 scopus 로고    scopus 로고
    • For a theoretical investigation of the influence of alkene functionality on thiol-ene kinetics, see: Northrop, B. H.; Coffey, R. N. J. Am. Chem. Soc. 2012, 134, 13804
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 13804
    • Northrop, B.H.1    Coffey, R.N.2
  • 63
    • 84865415630 scopus 로고    scopus 로고
    • Chemical Kinetics I: Rate Laws
    • University Science Books: Sausalito, CA
    • McQuarrie, D. A.; Simon, J. D. Chemical Kinetics I: Rate Laws. In Physical Chemistry: A Molecular Approach; University Science Books: Sausalito, CA, 1997; pp 1165-1169.
    • (1997) Physical Chemistry: A Molecular Approach , pp. 1165-1169
    • McQuarrie, D.A.1    Simon, J.D.2
  • 64
    • 56449103092 scopus 로고    scopus 로고
    • version 3.82; (accessed Aug 2, 2013)
    • Ianni, J. C. Kintecus, version 3.82; 2005. www.kintecus.com (accessed Aug 2, 2013).
    • (2005) Kintecus
    • Ianni, J.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.