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Volumn 56, Issue 28, 2015, Pages 4180-4183

Carbonyl olefination of diaryl ketones with heteroaryl sulfoxides

Author keywords

Fluorine; Olefination; Sulfoxide

Indexed keywords

CARBONYL DERIVATIVE; DIARYL KETONE; SULFOXIDE;

EID: 84930929799     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2015.05.034     Document Type: Article
Times cited : (13)

References (54)
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    • For some applications of Julia-Kocienski olefination, see: (a)
    • For some applications of Julia-Kocienski olefination, see: (a) A. Fettes, and E.M. Carreira J. Org. Chem. 68 2003 9274
    • (2003) J. Org. Chem. , vol.68 , pp. 9274
    • Fettes, A.1    Carreira, E.M.2
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    • 84911946791 scopus 로고    scopus 로고
    • Selected reviews on sulfinate (sulfinic acid) chemistry: (a)
    • Selected reviews on sulfinate (sulfinic acid) chemistry: (a) J. Aziz, S. Messaoudi, M. Alami, and A. Hamze Org. Biomol. Chem. 12 2014 9743
    • (2014) Org. Biomol. Chem. , vol.12 , pp. 9743
    • Aziz, J.1    Messaoudi, S.2    Alami, M.3    Hamze, A.4
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    • For the synthesis of fluoroalkenes via Julia-Kocienski olefination, see: (a)
    • For the synthesis of fluoroalkenes via Julia-Kocienski olefination, see: (a) A.K. Ghosh, and B. Zajc Org. Lett. 8 2006 1553
    • (2006) Org. Lett. , vol.8 , pp. 1553
    • Ghosh, A.K.1    Zajc, B.2
  • 34
    • 84930928954 scopus 로고    scopus 로고
    • See the Supporting information for reaction condition optimization.
    • See the Supporting information for reaction condition optimization.
  • 42
    • 84922814742 scopus 로고    scopus 로고
    • For some applications of fluoroolefins on the basis of their electrophilic properties, see: (a)
    • For some applications of fluoroolefins on the basis of their electrophilic properties, see: (a) B. Gao, Y. Zhao, and J. Hu Angew. Chem., Int. Ed. 54 2015 638
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 638
    • Gao, B.1    Zhao, Y.2    Hu, J.3
  • 54
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    • The intramolecular nucleophilic attack of a pyridyl motif to an in situ generated sulfonyl iodide and subsequent fragmentation was also observed in one of our previous works.
    • The intramolecular nucleophilic attack of a pyridyl motif to an in situ generated sulfonyl iodide and subsequent fragmentation was also observed in one of our previous works. Y. Zhao, B. Gao, and J. Hu J. Am. Chem. Soc. 134 2012 5790
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 5790
    • Zhao, Y.1    Gao, B.2    Hu, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.