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Volumn 20, Issue 52, 2014, Pages 17315-17318

Selective and scalable synthesis of trifluoromethanesulfenamides and fluorinated unsymmetrical disulfides using a shelf-stable electrophilic SCF3 reagent

Author keywords

Fluorine; S N bond formation; Sulfenamides; Synthetic methods; Trifluoromethanesulfenylation

Indexed keywords

AMINES; CHEMICAL COMPOUNDS; FLUORINE; FUNCTIONAL GROUPS; STEEL BEAMS AND GIRDERS;

EID: 84920135185     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201405654     Document Type: Article
Times cited : (37)

References (88)
  • 9
    • 33845183598 scopus 로고
    • For chemistry, synthetic methods and application of sulfenamides, see: a)
    • For chemistry, synthetic methods and application of sulfenamides, see: a) L. Craine, M. Raban, Chem. Rev. 1989, 89, 689-712
    • (1989) Chem. Rev. , vol.89 , pp. 689-712
    • Craine, L.1    Raban, M.2
  • 10
    • 26844557558 scopus 로고    scopus 로고
    • and references therein
    • b) I. V. Koval, Russ. Chem. Rev. 1996, 65, 421-440, and references therein.
    • (1996) Russ. Chem. Rev. , vol.65 , pp. 421-440
    • Koval, I.V.1
  • 11
    • 35649001352 scopus 로고    scopus 로고
    • (Eds.: V.J. Stella, R. T. Borchardt, M.J. Hageman, R. Oliyai, H. Maag, J.W. Tilley), AAPS Press/Springer, New York
    • a) V. R. Guarino, V.J. Stella in Prodrugs: Challenges and Rewards - Part 2 (Eds.: V.J. Stella, R. T. Borchardt, M.J. Hageman, R. Oliyai, H. Maag, J.W. Tilley), AAPS Press/Springer, New York, 2007, 133-188
    • (2007) Prodrugs: Challenges and Rewards - Part , vol.2 , pp. 133-188
    • Guarino, V.R.1    Stella, V.J.2
  • 17
    • 77958605423 scopus 로고    scopus 로고
    • and references cited therein
    • a) V.N. Boiko, Beilstein J. Org. Chem. 2010, 6, 880-921 and references cited therein
    • (2010) Beilstein J. Org. Chem. , vol.6 , pp. 880-921
    • Boiko, V.N.1
  • 19
    • 84886605746 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 6952-6954
    • (2013) Angew. Chem. , vol.125 , pp. 6952-6954
  • 48
    • 84874441007 scopus 로고    scopus 로고
    • Angew. Chem. 2009, 121, 8703-8707
    • (2009) Angew. Chem. , vol.121 , pp. 8703-8707
  • 52
    • 84875155345 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 10528-10531
    • (2012) Angew. Chem. , vol.124 , pp. 10528-10531
  • 55
    • 84888626008 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 11014-11017
    • (2013) Angew. Chem. , vol.125 , pp. 11014-11017
  • 60
    • 84879362108 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 3541-3544
    • (2013) Angew. Chem. , vol.125 , pp. 3541-3544
  • 62
    • 84888624325 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 13098-13102
    • (2013) Angew. Chem. , vol.125 , pp. 13098-13102
  • 66
    • 84888596412 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 13093-13097
    • (2013) Angew. Chem. , vol.125 , pp. 13093-13097
  • 82
    • 84906782370 scopus 로고    scopus 로고
    • During the preparation of this manuscript a new method for the preparation of trifluoromethylsulfenamides was reported:
    • During the preparation of this manuscript a new method for the preparation of trifluoromethylsulfenamides was reported: C. Xu, B. Ma, Q. Shen, Angew. Chem. Int. Ed. 2014, 53, 9316-9320
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 9316-9320
    • Xu, C.1    Ma, B.2    Shen, Q.3
  • 83
    • 84920201407 scopus 로고    scopus 로고
    • However, our method allows a selective introduction of trifluoromethylsulfenamide moiety into molecules with two different amino groups
    • Angew. Chem. 2014, 126, 9470-9474. However, our method allows a selective introduction of trifluoromethylsulfenamide moiety into molecules with two different amino groups.
    • (2014) Angew. Chem. , vol.126 , pp. 9470-9474


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.