메뉴 건너뛰기




Volumn 351, Issue 3, 2009, Pages 319-324

Ligand-free silver(I)-catalyzed intramolecular friedel-crafts alkylation of arenes with allylic alcohols

Author keywords

Alkylation; Aromatic compounds; Catalysis; Friedel crafts reaction; Silver

Indexed keywords


EID: 60849101850     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200800628     Document Type: Article
Times cited : (36)

References (64)
  • 1
    • 30744446209 scopus 로고    scopus 로고
    • For general review see: a
    • For general review see: a) K. Tatsuta, S. Hosokawa, Chem. Rev. 2005, 105, 4707-4729.
    • (2005) Chem. Rev , vol.105 , pp. 4707-4729
    • Tatsuta, K.1    Hosokawa, S.2
  • 2
    • 0001108788 scopus 로고    scopus 로고
    • a) G. Dyker, Angew. Chem. 1999, 111, 1808-1822;
    • (1999) Angew. Chem , vol.111 , pp. 1808-1822
    • Dyker, G.1
  • 3
    • 0033553817 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 1698-1712;
    • (1999) Angew. Chem. Int. Ed , vol.38 , pp. 1698-1712
  • 11
    • 38049017956 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 258-297.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 258-297
  • 12
    • 4544324311 scopus 로고    scopus 로고
    • Pd catalysis: a M. Bandini, A. Melloni, A. UmaniRonchi, Org. Lett. 2004, 6, 3199-3202;
    • Pd catalysis: a) M. Bandini, A. Melloni, A. UmaniRonchi, Org. Lett. 2004, 6, 3199-3202;
  • 23
    • 31444456960 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 793-796;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 793-796
  • 31
    • 1042276935 scopus 로고    scopus 로고
    • and references cited therein;
    • Angew. Chem. Int. Ed. 2004, 43, 550-556, and references cited therein;
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 550-556
  • 33
    • 0037193031 scopus 로고    scopus 로고
    • The use of mixture of Brønsted acids (TFA/AcOH) as the solvent in intramolecular FC alkylation of corresponding acetates has known to provide 4 in good yields: a) S. Ma, J. Zhang, Tetrahedron Lett. 2002, 43, 3435;
    • The use of mixture of Brønsted acids (TFA/AcOH) as the solvent in intramolecular FC alkylation of corresponding acetates has known to provide 4 in good yields: a) S. Ma, J. Zhang, Tetrahedron Lett. 2002, 43, 3435;
  • 35
    • 48849106814 scopus 로고    scopus 로고
    • 2 as promoter for arylenes cyclization: K. Namba, H. Yamamoto, I. Sasaki, K. Mori, H. Imagawa, M. Nishizawa, Org. Lett. 2008, 10, 1767-1770.
    • 2 as promoter for arylenes cyclization: K. Namba, H. Yamamoto, I. Sasaki, K. Mori, H. Imagawa, M. Nishizawa, Org. Lett. 2008, 10, 1767-1770.
  • 39
    • 34248637761 scopus 로고    scopus 로고
    • For some representative reviews of Au-catalyzed reactions see: a
    • For some representative reviews of Au-catalyzed reactions see: a) A. S. K. Hashmi, G. J. Hutchings, Angew. Chem. 2006, 118, 8064-8105;
    • (2006) Angew. Chem , vol.118 , pp. 8064-8105
    • Hashmi, A.S.K.1    Hutchings, G.J.2
  • 40
    • 33845546747 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 7896-7936;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 7896-7936
  • 41
    • 34547510627 scopus 로고    scopus 로고
    • b) A. S. K. Hashmi, Chem. Rev. 2007, 107, 3180-3211;
    • (2007) Chem. Rev , vol.107 , pp. 3180-3211
    • Hashmi, A.S.K.1
  • 43
    • 40949091926 scopus 로고    scopus 로고
    • d) H. C. Shen, Tetrahedron 2008, 64, 3885-3903;
    • (2008) Tetrahedron , vol.64 , pp. 3885-3903
    • Shen, H.C.1
  • 46
    • 51249100498 scopus 로고    scopus 로고
    • g) A. Arcadi, Chem. Rev. 2008, 108, 3266-3325;
    • (2008) Chem. Rev , vol.108 , pp. 3266-3325
    • Arcadi, A.1
  • 49
    • 60849087271 scopus 로고    scopus 로고
    • 3)AuCl]/AgOTf= 229.30 €/g and AgOTf (> 99%)=25.30 €/g
    • 3)AuCl]/AgOTf= 229.30 €/g and AgOTf (> 99%)=25.30 €/g
  • 51
    • 0034600902 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 2285-2288;
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 2285-2288
  • 60
    • 60849139320 scopus 로고    scopus 로고
    • Acyclic precursors carrying electron-withdrawing substituents on the aromatic ring proved to be inert under Ag catalysis
    • Acyclic precursors carrying electron-withdrawing substituents on the aromatic ring proved to be inert under Ag catalysis.
  • 62
    • 60849099829 scopus 로고    scopus 로고
    • See Supporting Information for details
    • See Supporting Information for details.
  • 64
    • 51049115331 scopus 로고    scopus 로고
    • For a recent review on enantioselective silver-catalyzed reactions see
    • For a recent review on enantioselective silver-catalyzed reactions see: M. Naodovic, H. Yamamoto, Chem. Rev. 2008, 108, 3132-3148.
    • (2008) Chem. Rev , vol.108 , pp. 3132-3148
    • Naodovic, M.1    Yamamoto, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.