메뉴 건너뛰기




Volumn 81, Issue 17, 2016, Pages 7486-7509

N-Trifluoromethylthio-dibenzenesulfonimide: A Shelf-Stable, Broadly Applicable Electrophilic Trifluoromethylthiolating Reagent

Author keywords

[No Author keywords available]

Indexed keywords

CHEMISTRY; ORGANIC COMPOUNDS;

EID: 84984914538     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/acs.joc.6b01178     Document Type: Article
Times cited : (164)

References (98)
  • 40
    • 84984917409 scopus 로고
    • 3 was reported to have an LCt50 of about 200 ppm/min
    • 3 was reported to have an LCt50 of about 200 ppm/min. Chem. Eng. News 1967, 45 (51), 44.
    • (1967) Chem. Eng. News , vol.45 , Issue.51 , pp. 44
  • 60
    • 84898740484 scopus 로고    scopus 로고
    • Xu, C.; Shen, Q. Org. Lett. 2014, 16, 2046 10.1021/ol5006533
    • (2014) Org. Lett. , vol.16 , pp. 2046
    • Xu, C.1    Shen, Q.2
  • 72
    • 84941896820 scopus 로고    scopus 로고
    • Xu, C.; Shen, Q. Org. Lett. 2015, 17, 4561 10.1021/acs.orglett.5b02315
    • (2015) Org. Lett. , vol.17 , pp. 4561
    • Xu, C.1    Shen, Q.2
  • 82
    • 84979493147 scopus 로고    scopus 로고
    • During the preparation of this manuscript, Zhao and co-workers reported an orgnocatalytic asymmetric trifluioromethylthiolating latonization reaction using 7 as the electrophilic trifluoromethylthiolating reagent. However, the excellent electrophilicity of reagent 7 was not recognized. In addition, reagent 7 used in Zhao's work was roughly 90% pure
    • During the preparation of this manuscript, Zhao and co-workers reported an orgnocatalytic asymmetric trifluioromethylthiolating latonization reaction using 7 as the electrophilic trifluoromethylthiolating reagent. However, the excellent electrophilicity of reagent 7 was not recognized. In addition, reagent 7 used in Zhao's work was roughly 90% pure. Liu, X.; An, R.; Zhang, X.-L.; Luo, J.; Zhao, X.-D. Angew. Chem., Int. Ed. 2016, 55, 5846 10.1002/anie.201601713
    • (2016) Angew. Chem., Int. Ed. , vol.55 , pp. 5846
    • Liu, X.1    An, R.2    Zhang, X.-L.3    Luo, J.4    Zhao, X.-D.5
  • 83
    • 84984880899 scopus 로고    scopus 로고
    • Shanghai Institute of Organic Chemistry. A provisional patent (application no. CN201510051839.2) on the preparation of reagent 7, its single-crystal structure, and its reactions with a variety of nucleophiles was filed on January 30
    • Shanghai Institute of Organic Chemistry. Electrophilic trifluoromethylthiolating reagent, its preparation and applications. A provisional patent (application no. CN201510051839.2) on the preparation of reagent 7, its single-crystal structure, and its reactions with a variety of nucleophiles was filed on January 30, 2015.
    • (2015) Electrophilic Trifluoromethylthiolating Reagent, Its Preparation and Applications.
  • 85
    • 84983187869 scopus 로고    scopus 로고
    • Reactions of imidazol(1,2-α)pyridines or pyrroles with an electrophilic trifluoromethylthiolating reagent in the presence of a Lewis acid or copper catalyst have been reported previously. and also see refs 13c, 16i
    • Reactions of imidazol(1,2-α)pyridines or pyrroles with an electrophilic trifluoromethylthiolating reagent in the presence of a Lewis acid or copper catalyst have been reported previously. Jiang, L.-Q.; Qian, J.-L.; Yi, W.-B.; Lu, G.-P.; Cai, C.; Zhang, W. Angew. Chem., Int. Ed. 2015, 54, 14965 and also see refs 13c, 16i. 10.1002/anie.201508495
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 14965
    • Jiang, L.-Q.1    Qian, J.-L.2    Yi, W.-B.3    Lu, G.-P.4    Cai, C.5    Zhang, W.6
  • 97
    • 84952685494 scopus 로고    scopus 로고
    • For reaction of an electrophilic trifluoromethylthiolating reagent with α β-unsaturated esters, see
    • For reaction of an electrophilic trifluoromethylthiolating reagent with α,β-unsaturated esters, see: Xiao, Q.; He, Q.-J.; Li, J.-C.; Wang, J. Org. Lett. 2015, 17, 6090 10.1021/acs.orglett.5b03116
    • (2015) Org. Lett. , vol.17 , pp. 6090
    • Xiao, Q.1    He, Q.-J.2    Li, J.-C.3    Wang, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.