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Volumn 13, Issue 21, 2011, Pages 5882-5885

Nucleophilic ortho allylation of aryl and heteroaryl sulfoxides

Author keywords

[No Author keywords available]

Indexed keywords

SULFOXIDE;

EID: 80055097646     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol2025197     Document Type: Article
Times cited : (112)

References (51)
  • 1
    • 0042291889 scopus 로고    scopus 로고
    • Wiley-VCH: Weinheim, Germany
    • Astruc, D. Modern arene chemistry; Wiley-VCH: Weinheim, Germany, 2002; p 330.
    • (2002) Modern Arene Chemistry , pp. 330
    • Astruc, D.1
  • 19
    • 79957985277 scopus 로고    scopus 로고
    • Maulide has recently reported the reaction of β-ketoesters with arylsulfoxides in an elegant, metal-free approach for the α-arylation of carbonyl compounds
    • Maulide has recently reported the reaction of β-ketoesters with arylsulfoxides in an elegant, metal-free approach for the α-arylation of carbonyl compounds. Huang, X.; Maulide, N. J. Am. Chem. Soc. 2011, 133, 8510
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 8510
    • Huang, X.1    Maulide, N.2
  • 37
    • 0348072278 scopus 로고    scopus 로고
    • In, Gladysz, J. A. Curran, D. P. Horváth, I. T. Wiley-VCH: Weinheim
    • Curran, D. P. In The Handbook of Fluorous Chemistry, Gladysz, J. A.; Curran, D. P.; Horváth, I. T., Eds.; Wiley-VCH: Weinheim, 2004.
    • (2004) The Handbook of Fluorous Chemistry
    • Curran, D.P.1
  • 39
    • 80055082758 scopus 로고    scopus 로고
    • Kita observed the allylation of thiophene and furan sulfoxides using allyltributyltin. See ref 5b
    • Kita observed the allylation of thiophene and furan sulfoxides using allyltributyltin. See ref 5b.
  • 40
    • 80055092311 scopus 로고    scopus 로고
    • Kita has reported the allylation of the benzene ring in N -Ts 5-sulfoxy indoles using similar conditions. Interestingly, in Kita's work the indole bearing a free N-H did not undergo productive allylation. See ref 5a
    • Kita has reported the allylation of the benzene ring in N -Ts 5-sulfoxy indoles using similar conditions. Interestingly, in Kita's work the indole bearing a free N-H did not undergo productive allylation. See ref 5a.
  • 41
    • 0038980571 scopus 로고    scopus 로고
    • For a review of hypervalent organosulfur compounds, see: Furukawa, N.; Sato, S. Top. Curr. Chem. 1999, 205, 89
    • (1999) Top. Curr. Chem. , vol.205 , pp. 89
    • Furukawa, N.1    Sato, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.