메뉴 건너뛰기




Volumn 47, Issue 28, 2008, Pages 5220-5223

Carbonyl propargylation from the alcohol or aldehyde oxidation level employing 1,3-enynes as surrogates to preformed allenylmetal reagents: A ruthenium-catalyzed C-C bond-forming transfer hydrogenation

Author keywords

Cross coupling; Enynes; Propargylation; Ruthenium; Transfer hydrogenation

Indexed keywords

ALDEHYDES; AROMATIC HYDROCARBONS; CARBONYLATION; CHEMICAL BONDS; CHEMICAL OXYGEN DEMAND; CHEMICAL REACTIONS; HYDROGEN; HYDROGENATION; IRON COMPOUNDS; ORGANIC COMPOUNDS; OXIDATION; RUTHENIUM;

EID: 48149091798     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200801359     Document Type: Article
Times cited : (89)

References (63)
  • 1
    • 0003627206 scopus 로고
    • For reviews that encompass carbonyl propargylation employing allenylmetal reagents, see: a, Ed, S. Patai, Wiley, New York
    • For reviews that encompass carbonyl propargylation employing allenylmetal reagents, see: a) J.-L. Moreau in The Chemistry of Ketenes, Allenes and Related Compounds (Ed.: S. Patai), Wiley, New York, 1980, pp. 363-413;
    • (1980) The Chemistry of Ketenes, Allenes and Related Compounds , pp. 363-413
    • Moreau, J.-L.1
  • 3
  • 21
    • 4243378570 scopus 로고
    • For selected reviews on ruthenium-catalyzed transfer hydrogenation, see: a
    • For selected reviews on ruthenium-catalyzed transfer hydrogenation, see: a) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069;
    • (1992) Chem. Rev , vol.92 , pp. 1051-1069
    • Zassinovich, G.1    Mestroni, G.2    Gladiali, S.3
  • 25
  • 26
    • 0001552544 scopus 로고    scopus 로고
    • e) R. Noyori, Angew. Chem. 2002, 114, 2108-2123;
    • (2002) Angew. Chem , vol.114 , pp. 2108-2123
    • Noyori, R.1
  • 27
    • 0037124885 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 2008-2022;
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 2008-2022
  • 29
    • 33646442062 scopus 로고    scopus 로고
    • g) K. Muñiz, Angew. Chem. 2005, 117, 6780-6785;
    • (2005) Angew. Chem , vol.117 , pp. 6780-6785
    • Muñiz, K.1
  • 30
    • 27444437031 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 6622-6627;
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 6622-6627
  • 34
    • 0035385137 scopus 로고    scopus 로고
    • For selected reviews of ruthenium-catalyzed C-C coupling, see: a
    • For selected reviews of ruthenium-catalyzed C-C coupling, see: a) B. M. Trost, F. D. Toste, A. B. Pinkerton, Chem. Rev. 2001, 101, 2067-2096;
    • (2001) Chem. Rev , vol.101 , pp. 2067-2096
    • Trost, B.M.1    Toste, F.D.2    Pinkerton, A.B.3
  • 37
    • 33846995439 scopus 로고    scopus 로고
    • For selected reviews on hydrogenative C-C coupling, see: a
    • For selected reviews on hydrogenative C-C coupling, see: a) M.-Y. Ngai, J.-R. Kong, M. J. Krische, J. Org. Chem. 2007, 72, 1063-1072;
    • (2007) J. Org. Chem , vol.72 , pp. 1063-1072
    • Ngai, M.-Y.1    Kong, J.-R.2    Krische, M.J.3
  • 40
    • 36049003722 scopus 로고    scopus 로고
    • The transformations may be considered as hydrogen autotransfer processes; for reviews, see: a
    • The transformations may be considered as hydrogen autotransfer processes; for reviews, see: a) G. Guillena, D. J. Ramón, M. Yus, Angew. Chem. 2007, 119, 2410-2416;
    • (2007) Angew. Chem , vol.119 , pp. 2410-2416
    • Guillena, G.1    Ramón, D.J.2    Yus, M.3
  • 41
    • 34250893845 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 2358-2364;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 2358-2364
  • 43
    • 1842788947 scopus 로고    scopus 로고
    • For rhodium-catalyzed reductive coupling of 1,3-enynes to carbonyl compounds and imines, see: a
    • For rhodium-catalyzed reductive coupling of 1,3-enynes to carbonyl compounds and imines, see: a) H.-Y. Jang, R. R. Huddleston, M. J. Krische, J. Am. Chem. Soc. 2004, 126, 4664-4668;
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 4664-4668
    • Jang, H.-Y.1    Huddleston, R.R.2    Krische, M.J.3
  • 48
    • 1842607439 scopus 로고    scopus 로고
    • For nickel-catalyzed reductive coupling of 1,3-enynes to carbonyl compounds, see: a
    • For nickel-catalyzed reductive coupling of 1,3-enynes to carbonyl compounds, see: a) K. M. Miller, T. Luanphaisarnnont, C. Molinaro, T. F. Jamison, J. Am. Chem. Soc. 2004, 126, 4130-4131;
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 4130-4131
    • Miller, K.M.1    Luanphaisarnnont, T.2    Molinaro, C.3    Jamison, T.F.4
  • 51
    • 0030861563 scopus 로고    scopus 로고
    • For seminal contributions to nickel-catalyzed alkyne/carbonyl reductive coupling, see: a
    • For seminal contributions to nickel-catalyzed alkyne/carbonyl reductive coupling, see: a) E. Oblinger, J. Montgomery, J. Am. Chem. Soc. 1997, 119, 9065-9066;
    • (1997) J. Am. Chem. Soc , vol.119 , pp. 9065-9066
    • Oblinger, E.1    Montgomery, J.2
  • 53
    • 11244320756 scopus 로고    scopus 로고
    • For reviews encompassing nickel-catalyzed alkyne/carbonyl reductive coupling, see: a
    • For reviews encompassing nickel-catalyzed alkyne/carbonyl reductive coupling, see: a) J. Montgomery, Angew. Chem. 2004, 116, 3980-3998;
    • (2004) Angew. Chem , vol.116 , pp. 3980-3998
    • Montgomery, J.1
  • 54
    • 4544323639 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 3890-3908;
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 3890-3908


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.