메뉴 건너뛰기




Volumn , Issue 25, 2011, Pages 4862-4867

Sulfoximines as a versatile scaffold for electrophilic fluoroalkylating reagents

Author keywords

Alkylation; Alkynes; Fluorine; Sulfoximines; Sulfur; Synthetic methods

Indexed keywords


EID: 80051963380     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201100503     Document Type: Article
Times cited : (63)

References (37)
  • 1
    • 80051972250 scopus 로고    scopus 로고
    • Selected references
    • Selected references
  • 29
    • 80052014650 scopus 로고    scopus 로고
    • The structure of these unfluorinated byproducts retaining an aromatic skeleton is under study
    • The structure of these unfluorinated byproducts retaining an aromatic skeleton is under study.
  • 30
    • 80051980081 scopus 로고    scopus 로고
    • As already noted by Hu and co-workers, a stoichiometric or an excess amount of the electrophilic reagent was detrimental to the yield.
    • As already noted by Hu and co-workers, a stoichiometric or an excess amount of the electrophilic reagent was detrimental to the yield.
  • 31
    • 80051966331 scopus 로고    scopus 로고
    • Sulfoximine 7c was entirely recovered at the end of the process.
    • Sulfoximine 7c was entirely recovered at the end of the process.
  • 32
    • 80051984398 scopus 로고    scopus 로고
    • The use of sulfoximine 1 was not considered because of its very poor solubility under the reaction conditions.
    • The use of sulfoximine 1 was not considered because of its very poor solubility under the reaction conditions.
  • 33
    • 77952859294 scopus 로고    scopus 로고
    • For other direct methods for trifluoromethylation of alkynes, see and references cited therein
    • For other direct methods for trifluoromethylation of alkynes, see: L. Chu, F.-L. Qing, J. Am. Chem. Soc. 2010, 132, 7262-7263 and references cited therein.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 7262-7263
    • Chu, L.1    Qing, F.-L.2
  • 36
    • 80051995766 scopus 로고    scopus 로고
    • We were not able to separate compound 11b from its dichlorofluoromethylated analog, but both structures were ascertained by NMR spectroscopy and mass spectrometry of the mixture (see Supporting Information)
    • We were not able to separate compound 11b from its dichlorofluoromethylated analog, but both structures were ascertained by NMR spectroscopy and mass spectrometry of the mixture (see Supporting Information).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.