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7
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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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9
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0003151465
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-
For a review for Friedläender quinoline synthesis, see:
-
For a review for Friedläender quinoline synthesis, see:. Cheng C.-C., and Yan S.-J. Org. React. 28 (1982) 37
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(1982)
Org. React.
, vol.28
, pp. 37
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-
Cheng, C.-C.1
Yan, S.-J.2
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10
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-
2342627915
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-
For a detailed mechanism for Friedläender quinoline synthesis, see:
-
For a detailed mechanism for Friedläender quinoline synthesis, see:. Muchowski J.M., and Maddox M.L. Can. J. Chem. 82 (2004) 461
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(2004)
Can. J. Chem.
, vol.82
, pp. 461
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Muchowski, J.M.1
Maddox, M.L.2
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12
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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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16
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0002946125
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For our recent report on ruthenium-catalyzed synthesis of indoles:
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For our recent report on ruthenium-catalyzed synthesis of indoles:. 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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19
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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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20
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0033582781
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For our recent report on ruthenium-catalyzed synthesis of quinolines:
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For our recent report on ruthenium-catalyzed synthesis of quinolines:. Cho C.S., Oh B.H., and Shim S.C. Tetrahedron Lett. 40 (1999) 1499
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(1999)
Tetrahedron Lett.
, vol.40
, pp. 1499
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Cho, C.S.1
Oh, B.H.2
Shim, S.C.3
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22
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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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23
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0002877215
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Cho C.S., Oh B.H., Kim J.S., Kim T.-J., and Shim S.C. Chem. Commun. (2000) 1885
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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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24
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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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25
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0001565788
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For ruthenium-catalyzed synthesis of N-heterocycles using alcohols:
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For ruthenium-catalyzed synthesis of N-heterocycles using alcohols:. Tsuji Y., Huh K.-T., and Watanabe Y. Tetrahedron Lett. 27 (1986) 377
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(1986)
Tetrahedron Lett.
, vol.27
, pp. 377
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Tsuji, Y.1
Huh, K.-T.2
Watanabe, Y.3
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27
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0002351285
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Kondo T., Yang S., Huh K.-T., Kobayashi M., Kotachi S., and Watanabe Y. Chem. Lett. (1991) 1275
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(1991)
Chem. Lett.
, pp. 1275
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Kondo, T.1
Yang, S.2
Huh, K.-T.3
Kobayashi, M.4
Kotachi, S.5
Watanabe, Y.6
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28
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33745628483
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note
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We confirmed in a separate experiment (run 3 of Table 1) that 2-hydroxyacetophenone is formed as an intermediate in 4% yield with complete conversion of 2a (99%) by GLC analysis.
-
-
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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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30
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0001951279
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Williams A.F., Floriani C., and Merbach A.E. (Eds), VCH Publishers, 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 Publishers, New York 463-486
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(1992)
Perspectives in Coordination Chemistry
, 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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