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Volumn 76, Issue 6, 2011, Pages 1707-1714

Selective synthetic routes to sterically hindered unsymmetrical diaryl ketones via arylstannanes

Author keywords

[No Author keywords available]

Indexed keywords

ARYLSTANNANES; CATALYST-FREE; DIARYL KETONES; ISOLATED YIELD; MEDIATED REACTIONS; O-DICHLOROBENZENE; RADICAL MECHANISM; REACTION PARTNERS; ROOM TEMPERATURE; SOLVENT FREE; SYNTHETIC ROUTES;

EID: 79953876699     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo102366q     Document Type: Article
Times cited : (26)

References (37)
  • 13
    • 0004063249 scopus 로고    scopus 로고
    • VCH Verlagsgesellschaft: Weinheim Germany
    • Davies, A. Organotin Chemistry; VCH Verlagsgesellschaft: Weinheim, Germany, 1997.
    • (1997) Organotin Chemistry
    • Davies, A.1
  • 16
    • 79953905320 scopus 로고    scopus 로고
    • The starting arylstannanes were prepared by known procedures (see the Supporting Information)
    • The starting arylstannanes were prepared by known procedures (see the Supporting Information).
  • 17
    • 84855621743 scopus 로고    scopus 로고
    • Anisole reacted with 2b and 2c under similar reaction conditions. After 2 h at 180 °C, ketones 4bb or 4bc were obtained as the only products
    • Anisole reacted with 2b and 2c under similar reaction conditions. After 2 h at 180 °C, ketones 4bb or 4bc were obtained as the only products.
  • 18
    • 79953896221 scopus 로고    scopus 로고
    • We inform the best result obtained after working at different concentrations
    • We inform the best result obtained after working at different concentrations.
  • 19
    • 79953908517 scopus 로고    scopus 로고
    • We inform the best result obtained after working at different temperatures
    • We inform the best result obtained after working at different temperatures.
  • 20
    • 79953881499 scopus 로고    scopus 로고
    • It should be mentioned that anisole reacted with 2a, 2d, and 2e, under similar reaction conditions, giving the corresponding p-isomers as main products
    • It should be mentioned that anisole reacted with 2a, 2d, and 2e, under similar reaction conditions, giving the corresponding p-isomers as main products.
  • 22
    • 0003003033 scopus 로고
    • Aromatic ketone synthesis
    • Olah, G. A., Ed.; Wiley- Interscience: New York
    • Gore, P. H. Aromatic Ketone Synthesis. In Friedel-Crafts and Related Reactions; Olah, G. A., Ed.; Wiley- Interscience: New York, 1964; Vol. III, p 1.
    • (1964) Friedel-Crafts and Related Reactions , Issue.3 , pp. 1
    • Gore, P.H.1
  • 23
    • 79953860403 scopus 로고    scopus 로고
    • The actual reaction conditions of the isomerization of 3db
    • The actual reaction conditions of the isomerization of 3db


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.