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Volumn , Issue 12, 2011, Pages 1761-1765

Synthesis of conjugated tri(hetero)aryl derivatives based on one-pot double Suzuki-miyaura couplings using bifunctional dipotassium phenylene-1,4- bis(trifluoroborate)

Author keywords

Suzuki Miyaura reaction; arylation; cross coupling; epoxides; terphenyls

Indexed keywords

ARYL BROMINE DERIVATIVE; BORIC ACID; BROMINE DERIVATIVE; DIPOTASSIUM PHENYLENE 1,4 BIS(TRIFLUOROBORATE); UNCLASSIFIED DRUG;

EID: 79960227989     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1260581     Document Type: Article
Times cited : (16)

References (52)
  • 19
    • 17744384723 scopus 로고    scopus 로고
    • The Suzuki cross-coupling reactions of symmetrical dihalobenzenes with arylboronic acids and esters have often led to mixtures of mono- and biscoupled products, albeit with a different selectivity according to the nature of both the halogen employed and the boron-containing species; for a survey, see:, Sinclair D J., Sherburn M S., J. Org. Chem. 2005 70 3730
    • (2005) J. Org. Chem. , vol.70 , pp. 3730
    • Sinclair, D.J.1    Sherburn, M.S.2
  • 20
    • 0036248017 scopus 로고    scopus 로고
    • The double Suzuki cross-coupling of phenyl-1,4-diboronic acid bispinacol ester with aryl halides has also been investigated
    • The double Suzuki cross-coupling of phenyl-1,4-diboronic acid bispinacol ester with aryl halides has also been investigated:, Chaumeil H, Drian C L., Defoin A, Synthesis 2002 757
    • (2002) Synthesis , pp. 757
    • Chaumeil, H.1    Drian, C.L.2    Defoin, A.3
  • 43
    • 33646514881 scopus 로고    scopus 로고
    • Double couplings on bromoiodobenzenes, promoted by an excess of phenylboronic acid, have often led to mixtures of mono- and diarylated products; see
    • Double couplings on bromoiodobenzenes, promoted by an excess of phenylboronic acid, have often led to mixtures of mono- and diarylated products; see:, Liu L, Zhang Y, Xin B, J. Org. Chem. 2006 71 3994
    • (2006) J. Org. Chem. , vol.71 , pp. 3994
    • Liu, L.1    Zhang, Y.2    Xin, B.3
  • 51
    • 70349970584 scopus 로고    scopus 로고
    • The use of boron reagents for orthogonal functionalization through Suzuki-Miyaura cross-couplings has recently been highlighted; see
    • The use of boron reagents for orthogonal functionalization through Suzuki-Miyaura cross-couplings has recently been highlighted; see:, Tobisu M, Chatani O, Angew. Chem. Int. Ed. 2009 48 3565
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 3565
    • Tobisu, M.1    Chatani, O.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.