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Volumn 17, Issue 43, 2011, Pages 12203-12209

Triflic acid catalyzed reductive coupling reactions of carbonyl compounds with O-, S-, and N-nucleophiles

Author keywords

Br nsted acids; reductive etherification; silanes; sulfonamides; thioethers

Indexed keywords

CATALYTIC CONDITIONS; FUNCTIONALIZATIONS; HIGH YIELD; REDUCTIVE COUPLING REACTION; REDUCTIVE ETHERIFICATION; SHORT REACTION TIME; SULFONAMIDES; THIOETHERS; TRIFLIC ACIDS;

EID: 80054019414     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201101819     Document Type: Article
Times cited : (61)

References (39)
  • 32
    • 33646714554 scopus 로고    scopus 로고
    • It is known, that nitromethane enhances the reactivity of cerium(III) triflate in a range of reactions, see.
    • It is known, that nitromethane enhances the reactivity of cerium(III) triflate in a range of reactions, see:, G. Bartoli, A. De Nino, R. Dalpozzo, L. Maiuolo, M. Nardi, A. Procopio, A. Tagerelli, Lett. Org. Chem. 2005, 2, 51-53.
    • (2005) Lett. Org. Chem. , vol.2 , pp. 51-53
    • Bartoli, G.1    De Nino, A.2    Dalpozzo, R.3    Maiuolo, L.4    Nardi, M.5    Procopio, A.6    Tagerelli, A.7
  • 33
    • 0029058108 scopus 로고
    • For an example of a cerium(III) perchlorate catalyzedreaction, see.
    • For an example of a cerium(III) perchlorate catalyzedreaction, see:, W.-S. Kim, S. Hosono, H. Sasai, M. Shibasaki, Tetrahedron Lett. 1995, 36, 4443-4446.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 4443-4446
    • Kim, W.-S.1    Hosono, S.2    Sasai, H.3    Shibasaki, M.4
  • 34
    • 0036625262 scopus 로고    scopus 로고
    • For a review on rare earth metal triflates in organic synthesis, see.
    • For a review on rare earth metal triflates in organic synthesis, see:, S. Kobayashi, M. Sugiura, H. Kitagawa, W. W.-L. Lam, Chem. Rev. 2002, 102, 2227-2302.
    • (2002) Chem. Rev. , vol.102 , pp. 2227-2302
    • Kobayashi, S.1    Sugiura, M.2    Kitagawa, H.3    Lam, W.W.-L.4
  • 35
    • 9344257839 scopus 로고
    • It is noteworthy, that stoichiometric amounts of triflic acid together with triethylsilane have been used for the reduction of carbonyl compounds to hydrocarbons, see.
    • It is noteworthy, that stoichiometric amounts of triflic acid together with triethylsilane have been used for the reduction of carbonyl compounds to hydrocarbons, see:, G. A. Olah, M. Arvanaghi, L. Ohannessian, Synthesis 1986, 770-772.
    • (1986) Synthesis , pp. 770-772
    • Olah, G.A.1    Arvanaghi, M.2    Ohannessian, L.3
  • 36
    • 33749000858 scopus 로고    scopus 로고
    • It has been shown before, that triflic acid can initiate reactions in a similar manner to metal triflates, see for example.
    • It has been shown before, that triflic acid can initiate reactions in a similar manner to metal triflates, see for example:, D. C. Rosenfeld, S. Shekhar, A. Takemiya, M. Utsunomiya, J. F. Hartwig, Org. Lett. 2006, 8, 4179-4182.
    • (2006) Org. Lett. , vol.8 , pp. 4179-4182
    • Rosenfeld, D.C.1    Shekhar, S.2    Takemiya, A.3    Utsunomiya, M.4    Hartwig, J.F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.