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Volumn , Issue 20, 2012, Pages 3759-3763

Near room temperature cross-coupling reactions of arene boronic acids with a quinoxaline 1,4-dioxide benzylsulfanyl derivative

Author keywords

Boron; Copper; Cross coupling; Heterocycles; Nitrogen oxides

Indexed keywords


EID: 84863676450     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201200433     Document Type: Article
Times cited : (9)

References (40)
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    • Leclerc, J.-P.1    Fagnou, K.2
  • 29
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    • Heterocyclic sulfonyl chlorides are often quite unstable and rapidly decompose with the loss of sulfur dioxide into the corresponding chloride derivatives:, R. O. Roblin, J. W. Clapp, J. Am. Chem. Soc. 1950, 72, 4890-4892.
    • (1950) J. Am. Chem. Soc. , vol.72 , pp. 4890-4892
    • Roblin, R.O.1    Clapp, J.W.2
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    • E. C. Taylor, G. W. H. Cheeseman, J. Am. Chem. Soc. 1964, 86, 1830-1835. Quinoxaline monoxide 9 could be obtained as a minor product next to 10 when 8 was oxidized as before with the omission of acetic anhydride.
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 1830-1835
    • Taylor, E.C.1    Cheeseman, G.W.H.2
  • 38
    • 57549083398 scopus 로고    scopus 로고
    • Contrary to the general trend in organometallic reactions, aryl chlorides are preferred substrates compared to iodides or bromides in iron-catalyzed cross-couplings:, B. D. Sherry, A. Fürstner, Acc. Chem. Res. 2008, 41, 1500-1511.
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1500-1511
    • Sherry, B.D.1    Fürstner, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.