메뉴 건너뛰기




Volumn , Issue 12, 2007, Pages 722-724

A first homogeneous gold(III)-catalysed epoxidation of aromatic alkenes

Author keywords

Alkenes; Epoxidations; Gold; Homogeneous catalysis; Sodium chlorite

Indexed keywords


EID: 44949155331     PISSN: 03082342     EISSN: None     Source Type: Journal    
DOI: 10.3184/030823407X275937     Document Type: Article
Times cited : (7)

References (51)
  • 1
    • 8744259772 scopus 로고    scopus 로고
    • For reviews on gold-catalysed transformations see: a
    • For reviews on gold-catalysed transformations see: (a) A.S.K. Hashmi, Gold Bull., 2004, 37, 51;
    • (2004) Gold Bull , vol.37 , pp. 51
    • Hashmi, A.S.K.1
  • 28
    • 44949202436 scopus 로고    scopus 로고
    • A. von. Baeyer and V. Villiger, Ber. Dtsch. Chem. Ges., 1899, 32, 3622.
    • A. von. Baeyer and V. Villiger, Ber. Dtsch. Chem. Ges., 1899, 32, 3622.
  • 31
    • 0347723661 scopus 로고    scopus 로고
    • For selected heterogeneous epoxidation reactions of propene, see: a
    • For selected heterogeneous epoxidation reactions of propene, see: (a) T. Hayshi, K. Tanaka and M. Haruta, J. Catal. 1998, 178, 566;
    • (1998) J. Catal , vol.178 , pp. 566
    • Hayshi, T.1    Tanaka, K.2    Haruta, M.3
  • 33
    • 33747852637 scopus 로고    scopus 로고
    • For heterogeneous epoxidation reactions of styrene, see
    • (c) T.A. Nijhuis and B.M. Weckhuysen, Catal. Today, 2006, 117, 84; For heterogeneous epoxidation reactions of styrene, see:
    • (2006) Catal. Today , vol.117 , pp. 84
    • Nijhuis, T.A.1    Weckhuysen, B.M.2
  • 37
    • 85127386022 scopus 로고    scopus 로고
    • 2, Oxone, NaOCl, and PhIO did not give epoxidation product, only trace amount of C-C double bond cleavage products were detected.
    • 2, Oxone, NaOCl, and PhIO did not give epoxidation product, only trace amount of C-C double bond cleavage products were detected.
  • 38
    • 44949162850 scopus 로고    scopus 로고
    • See Supplementary Data for details
    • See Supplementary Data for details.
  • 39
    • 37049110274 scopus 로고    scopus 로고
    • For the preparation of chloro(triphenylphosphine)gold(I), see: K. Burgess, B.F.G. Johnson, J. Lewis and P.R. Raithby J. Chem. Soc., Dalton Trans., 1983, 1661.
    • For the preparation of chloro(triphenylphosphine)gold(I), see: K. Burgess, B.F.G. Johnson, J. Lewis and P.R. Raithby J. Chem. Soc., Dalton Trans., 1983, 1661.
  • 40
    • 37049075410 scopus 로고    scopus 로고
    • For the preparation of dichloro(pyridine-2-carboxylato)gold(III), see: (a) A. Dar, K. Moss, S. M. Cottrill, R.V. Parish, C.A. McAuliffe, R.G. Pritchard, B. Beagley and J. Sandbank, J. Chem. Soc., Dalton Trans., 1992,1907; For applications of dichloro(pyridine-2-carboxylato)gold(III), see:
    • For the preparation of dichloro(pyridine-2-carboxylato)gold(III), see: (a) A. Dar, K. Moss, S. M. Cottrill, R.V. Parish, C.A. McAuliffe, R.G. Pritchard, B. Beagley and J. Sandbank, J. Chem. Soc., Dalton Trans., 1992,1907; For applications of dichloro(pyridine-2-carboxylato)gold(III), see:
  • 44
    • 85127371764 scopus 로고    scopus 로고
    • 3: B.C. Ranu and U. Jana, J. Org. Chem., 1998, 63, 8212;
    • 3: B.C. Ranu and U. Jana, J. Org. Chem., 1998, 63, 8212;
  • 45
    • 85127379060 scopus 로고    scopus 로고
    • 3: A. Procopio, R. Dalpozzo, A.N. Nino, M. Nardi, G. Sindona and A. Tagarelli, Synlett, 2004, 14, 2633;
    • 3: A. Procopio, R. Dalpozzo, A.N. Nino, M. Nardi, G. Sindona and A. Tagarelli, Synlett, 2004, 14, 2633;
  • 46
    • 85127436887 scopus 로고    scopus 로고
    • 3: K.A. Bhatia, K.J. Eash, N.M. Leoard, M.C. Oswald and R.S. Mohan, Tetrahedron Lett., 2001, 42, 8129;
    • 3: K.A. Bhatia, K.J. Eash, N.M. Leoard, M.C. Oswald and R.S. Mohan, Tetrahedron Lett., 2001, 42, 8129;
  • 48
    • 0028265116 scopus 로고    scopus 로고
    • K. Maruoka, N. Murase, R. Bureau, T. Ooi and H. Yamamoto, Tetrahedron, 1994, 50, 3663;
    • (a) K. Maruoka, N. Murase, R. Bureau, T. Ooi and H. Yamamoto, Tetrahedron, 1994, 50, 3663;


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.