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1
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84944067367
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Katritzky A.R., and Rees C.W. (Eds), Pergamon, New York
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Jones G. In: Katritzky A.R., and Rees C.W. (Eds). Comprehensive Heterocyclic Chemistry Vol. 2 (1984), Pergamon, New York 395
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Comprehensive Heterocyclic Chemistry
, vol.2
, pp. 395
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Jones, G.1
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4
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0002877215
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and references cited therein
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Cho C.S., Oh B.H., Kim J.S., Kim T.-J., and Shim S.C. Chem. Commun. (2000) 1885 and references cited therein
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(2000)
Chem. Commun.
, pp. 1885
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Cho, C.S.1
Oh, B.H.2
Kim, J.S.3
Kim, T.-J.4
Shim, S.C.5
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7
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0034703278
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Cho C.S., Kim J.S., Oh B.H., Kim T.-J., and Shim S.C. Tetrahedron 56 (2000) 7747
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(2000)
Tetrahedron
, vol.56
, pp. 7747
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Cho, C.S.1
Kim, J.S.2
Oh, B.H.3
Kim, T.-J.4
Shim, S.C.5
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8
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0036568916
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Cho C.S., Kim T.K., Kim B.T., Kim T.-J., and Shim S.C. J. Organomet. Chem. 650 (2002) 65
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(2002)
J. Organomet. Chem.
, vol.650
, pp. 65
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Cho, C.S.1
Kim, T.K.2
Kim, B.T.3
Kim, T.-J.4
Shim, S.C.5
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10
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0002946125
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For our recent report on synthesis of indoles via similar ruthenium-catalyzed alkanol group transfer from alkanolamines to N-atom of anilines:
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For our recent report on synthesis of indoles via similar ruthenium-catalyzed alkanol group transfer from alkanolamines to N-atom of anilines:. Cho C.S., Lim H.K., Shim S.C., Kim T.J., and Choi H.-J. Chem. Commun. (1998) 995
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(1998)
Chem. Commun.
, pp. 995
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Cho, C.S.1
Lim, H.K.2
Shim, S.C.3
Kim, T.J.4
Choi, H.-J.5
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13
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0037474671
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Cho C.S., Kim J.H., Choi H.-J., Kim T.-J., and Shim S.C. Tetrahedron Lett. 44 (2003) 2975
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(2003)
Tetrahedron Lett.
, vol.44
, pp. 2975
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Cho, C.S.1
Kim, J.H.2
Choi, H.-J.3
Kim, T.-J.4
Shim, S.C.5
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18
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0141517572
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Cho C.S., Kim B.T., Choi H.-J., Kim T.-J., and Shim S.C. Tetrahedron 59 (2003) 7997
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(2003)
Tetrahedron
, vol.59
, pp. 7997
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Cho, C.S.1
Kim, B.T.2
Choi, H.-J.3
Kim, T.-J.4
Shim, S.C.5
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19
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3142700696
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For similar ruthenium- and iridium-catalyzed oxidative cyclization of 2-aminobenzyl alcohol with ketones leading to quinolines:
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For similar ruthenium- and iridium-catalyzed oxidative cyclization of 2-aminobenzyl alcohol with ketones leading to quinolines:. Motokura K., Mizugaki T., Ebitani K., and Kaneda K. Tetrahedron Lett. 45 (2004) 6029
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(2004)
Tetrahedron Lett.
, vol.45
, pp. 6029
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Motokura, K.1
Mizugaki, T.2
Ebitani, K.3
Kaneda, K.4
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22
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0035966201
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It has recently been found that carbonyl compounds (or secondary alcohols) are coupled with primary alcohols in the presence of a ruthenium catalyst and a base:
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It has recently been found that carbonyl compounds (or secondary alcohols) are coupled with primary alcohols in the presence of a ruthenium catalyst and a base:. Cho C.S., Kim B.T., Kim T.-J., and Shim S.C. J. Org. Chem. 66 (2001) 9020
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(2001)
J. Org. Chem.
, vol.66
, pp. 9020
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Cho, C.S.1
Kim, B.T.2
Kim, T.-J.3
Shim, S.C.4
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24
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0041428071
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Cho C.S., Kim B.T., Kim H.-S., Kim T.-J., and Shim S.C. Organometallics 22 (2003) 3608
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(2003)
Organometallics
, vol.22
, pp. 3608
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Cho, C.S.1
Kim, B.T.2
Kim, H.-S.3
Kim, T.-J.4
Shim, S.C.5
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27
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0035912306
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For a regioselective Friedländer quinoline synthesis, see:
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For a regioselective Friedländer quinoline synthesis, see:. Hsiao Y., Rivera N.R., Yasuda N., Hughes D.L., and Reider P.J. Org. Lett. 3 (2001) 1101
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(2001)
Org. Lett.
, vol.3
, pp. 1101
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Hsiao, Y.1
Rivera, N.R.2
Yasuda, N.3
Hughes, D.L.4
Reider, P.J.5
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29
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4243378570
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For recent reviews on transition metal-catalyzed transfer hydrogenation, see:
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For recent reviews on transition metal-catalyzed transfer hydrogenation, see:. Zassinovich G., Mestroni G., and Gladiali S. Chem. Rev. 92 (1992) 1051
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(1992)
Chem. Rev.
, vol.92
, pp. 1051
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Zassinovich, G.1
Mestroni, G.2
Gladiali, S.3
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0001951279
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Williams A.F., Floriani C., and Merbach A.E. (Eds), VCH, New York
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Bäckvall J.-E., Chowdhury R.L., Karlsson U., and Wang G. In: Williams A.F., Floriani C., and Merbach A.E. (Eds). Perspectives in Coordination Chemistry (1992), VCH, New York 463-486
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(1992)
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, pp. 463-486
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Bäckvall, J.-E.1
Chowdhury, R.L.2
Karlsson, U.3
Wang, G.4
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34
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33747176717
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For ruthenium-catalyzed oxidative cyclization of 2-aminobenzyl alcohol with aldehydes leading to 3-substituted quinolines
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For ruthenium-catalyzed oxidative cyclization of 2-aminobenzyl alcohol with aldehydes leading to 3-substituted quinolines. Cho C.S., Ren W.X., and Shim S.C. Bull. Korean Chem. Soc. 26 (2005) 2038
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(2005)
Bull. Korean Chem. Soc.
, vol.26
, pp. 2038
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Cho, C.S.1
Ren, W.X.2
Shim, S.C.3
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35
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0003678023
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American Chemical Society, Washington, DC pp 114-126
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Hudlický M. Oxidation in Organic Chemistry (1990), American Chemical Society, Washington, DC pp 114-126
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(1990)
Oxidation in Organic Chemistry
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Hudlický, M.1
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36
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33747156264
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note
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2/KOH catalytic system, however, benzyl alcohol was not effectively oxidized to benzaldehyde (11% yield) under the same catalytic system.
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