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Volumn 50, Issue 27, 2011, Pages 6142-6146

Coupling of quinone monoacetals promoted by sandwiched Brønsted acids: Synthesis of oxygenated biaryls

Author keywords

biaryls; C C coupling; chemoselectivity; heterocycles; natural products

Indexed keywords

BIARYLS; C-C COUPLING; CHEMO-SELECTIVITY; HETEROCYCLES; NATURAL PRODUCTS;

EID: 79959493898     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201101646     Document Type: Article
Times cited : (58)

References (46)
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    • Phenoxenium would be generated under acidic conditions from quinone monoacetals. It seems difficult to react with aromatic nucleohpiles at the αposition of the carbonyl group. See the discussion in.
    • Phenoxenium would be generated under acidic conditions from quinone monoacetals. It seems difficult to react with aromatic nucleohpiles at the αposition of the carbonyl group. See the discussion in:, A. Jean, J. Cantat, D. Berard, D. Bouchu, S. Canesi, Org. Lett. 2007, 9, 2553.
    • (2007) Org. Lett. , vol.9 , pp. 2553
    • Jean, A.1    Cantat, J.2    Berard, D.3    Bouchu, D.4    Canesi, S.5
  • 30
    • 0344092053 scopus 로고    scopus 로고
    • avalues of solid polyoxometalates were observed in alcohol solvents.,. See also ref.[8c].
    • avalues of solid polyoxometalates were observed in alcohol solvents., M. N. Timofeeva, M. M. Matrosova, G. M. Maksimov, V. A. Likholobov, Kinet. Katal. 2001, 42, 862. See also ref.[8c].
    • (2001) Kinet. Katal. , vol.42 , pp. 862
    • Timofeeva, M.N.1    Matrosova, M.M.2    Maksimov, G.M.3    Likholobov, V.A.4
  • 38
    • 79959516784 scopus 로고    scopus 로고
    • As well as other electron-rich aromatic and heteroaromatic compounds, typical silylated carbon nuclophiles can be introduced to quinone monoacetals 1 by the methodology
    • As well as other electron-rich aromatic and heteroaromatic compounds, typical silylated carbon nuclophiles can be introduced to quinone monoacetals 1 by the methodology.
  • 42
    • 66249141970 scopus 로고    scopus 로고
    • references therein; for a review, see
    • C. A. James, V. Snieckus, J. Org. Chem. 2009, 74, 4080, and references therein; for a review, see
    • (2009) J. Org. Chem. , vol.74 , pp. 4080
    • James, C.A.1    Snieckus, V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.