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Volumn 52, Issue 34, 2011, Pages 4405-4407

Palladium-catalyzed benzoin-mediated redox process leading to biaryls from aryl halides

Author keywords

Benzoin; Biaryls; Palladium; Redox process; Reductive coupling

Indexed keywords

BENZOIN; HALIDE; PALLADIUM;

EID: 79960847587     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.06.045     Document Type: Article
Times cited : (15)

References (45)
  • 5
    • 1942445158 scopus 로고    scopus 로고
    • For the leading references on metal-mediated homocoupling reactions, see: T.D. Nelson, and R.D. Crouch Org. React. 63 2004 265 555
    • (2004) Org. React. , vol.63 , pp. 265-555
    • Nelson, T.D.1    Crouch, R.D.2
  • 7
    • 0000658001 scopus 로고    scopus 로고
    • For the palladium-catalyzed reductive homocouplings in the presence of reducing agents, see: D.D. Hennings, T. Iwama, and V.H. Rawal Org. Lett. 1 1999 1205 1208
    • (1999) Org. Lett. , vol.1 , pp. 1205-1208
    • Hennings, D.D.1    Iwama, T.2    Rawal, V.H.3
  • 23
    • 64349089486 scopus 로고    scopus 로고
    • Wang and Lu have reported a Pd(II)-catalyzed cross-coupling of aryl iodides in the absence of an additional reducing agent, see
    • Wang and Lu have reported a Pd(II)-catalyzed cross-coupling of aryl iodides in the absence of an additional reducing agent, see: L. Wang, and W. Lu Org. Lett. 11 2009 1079 1082
    • (2009) Org. Lett. , vol.11 , pp. 1079-1082
    • Wang, L.1    Lu, W.2
  • 24
    • 4143153074 scopus 로고    scopus 로고
    • For palladium-catalyzed oxidation of alcohols, see: S.S. Stahl Angew. Chem., Int. Ed. 43 2004 3400 3420
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 3400-3420
    • Stahl, S.S.1
  • 35
    • 79251601341 scopus 로고    scopus 로고
    • For the base-mediated aerobic oxidation of benzoin to benzil, see: P. Muthupandi, and G. Sekar Tetrahedron Lett. 52 2011 692 695
    • (2011) Tetrahedron Lett. , vol.52 , pp. 692-695
    • Muthupandi, P.1    Sekar, G.2
  • 39
    • 79957961352 scopus 로고    scopus 로고
    • Very recently, we reported an expedient synthetic procedure of benzil derivatives from aryl bromides using vinylene carbonate in a palladium-catalyzed reaction. During the reaction we found that aryl bromides could be converted to biaryls by benzoin via a palladium-catalyzed redox process. Thus we examined the same conditions for the reductive aryl coupling of bromobenzene, see
    • Very recently, we reported an expedient synthetic procedure of benzil derivatives from aryl bromides using vinylene carbonate in a palladium-catalyzed reaction. During the reaction we found that aryl bromides could be converted to biaryls by benzoin via a palladium-catalyzed redox process. Thus we examined the same conditions for the reductive aryl coupling of bromobenzene, see: K.H. Kim, B.R. Park, J.W. Lim, and J.N. Kim Tetrahedron Lett. 52 2011 3463 3466
    • (2011) Tetrahedron Lett. , vol.52 , pp. 3463-3466
    • Kim, K.H.1    Park, B.R.2    Lim, J.W.3    Kim, J.N.4
  • 40
    • 79960848611 scopus 로고    scopus 로고
    • note
    • 3,5,10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.