-
13
-
-
47149087147
-
-
G.-D. Zhu V. B. Gandhi J. Gong S. Thomas Y. Luo X. Liu Y. Shi V. Klinghofer E. F. Johnson D. Frost C. Donawho K. Jarvis J. Bouska K. C. Marsh S. H. Rosenberg V. L. Giranda T. D Penning Bioorg. Med. Chem. Lett. 2008 18 3955.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 3955
-
-
Zhu, G.-D.1
Gandhi, V.B.2
Gong, J.3
Thomas, S.4
Luo, Y.5
Liu, X.6
Shi, Y.7
Klinghofer, V.8
Johnson, E.F.9
Frost, D.10
Donawho, C.11
Jarvis, K.12
Bouska, J.13
Marsh, K.C.14
Rosenberg, S.H.15
Giranda, V.L.16
Penning, T.D.17
-
14
-
-
51349162920
-
-
Y. Ogino N. Ohtake Y. Nagae K. Matsuda M. Moriya T. Suga M. Ishikawa M. Kanesaka Y. Mitobe J. Ito T. Kanno A. Ishiara H. Iwaasa T. Ohe A. Kanatani T. Fukami Bioorg. Med. Chem. Lett. 2008 18 5010.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 5010
-
-
Ogino, Y.1
Ohtake, N.2
Nagae, Y.3
Matsuda, K.4
Moriya, M.5
Suga, T.6
Ishikawa, M.7
Kanesaka, M.8
Mitobe, Y.9
Ito, J.10
Kanno, T.11
Ishiara, A.12
Iwaasa, H.13
Ohe, T.14
Kanatani, A.15
Fukami, T.16
-
23
-
-
0003607021
-
-
A. R. KatritzkyC. W. Rees, K. T. Potts,), Pergamon Press, New York
-
M. R. Grimmet, Comprehensive Heterocyclic Chemistry, (Ed.: A. R. KatritzkyC. W. Rees, K. T. Potts,), Pergamon Press, New York, 1984, Vol. 5.
-
(1984)
Comprehensive Heterocyclic Chemistry
, vol.5
-
-
Grimmet, M.R.1
-
24
-
-
0003593740
-
-
A. Weissberger, E. C. Taylor, John Wiley and Sons
-
P. N. Preston, Chemistry, of Heterocyclic Compounds (Ed.: A. Weissberger, E. C. Taylor, John Wiley and Sons, 1981, Vol. 40.
-
(1981)
Chemistry, of Heterocyclic Compounds
, vol.40
-
-
Preston, P.N.1
-
31
-
-
31544450237
-
-
For selected examples in selective synthesis of 2-substituted benzimidazole using o-phenylenediamine and aldehyde, see
-
For selected examples in selective synthesis of 2-substituted benzimidazole using o-phenylenediamine and aldehyde, see R. Trivedi S. K. De R. A. Gibbs J. Mol. Catal. A: Chem. 2006 245 8.
-
(2006)
J. Mol. Catal. A: Chem.
, vol.245
, pp. 8
-
-
Trivedi, R.1
De, S.K.2
Gibbs, R.A.3
-
38
-
-
34948893906
-
-
For typical example in selective synthesis of 1,2-disubstituted benzimidazoles using o-phenylenediamine and aldehyde, see
-
For typical example in selective synthesis of 1,2-disubstituted benzimidazoles using o-phenylenediamine and aldehyde, see N. D. Kokare J. N. Sangshetti D. B. Shinde Synthesis 2007 2829.
-
(2007)
Synthesis
, pp. 2829
-
-
Kokare, N.D.1
Sangshetti, J.N.2
Shinde, D.B.3
-
56
-
-
31044446976
-
-
J. Ishida H. Yamamoto Y. Kido K. Kamijo K. Murano H. Miyake M. Ohkubo T. Kinoshita M. Warizaya A. Iwashita K. Mihara N. Matsuoka K. Hattori Bioorg. Med. Chem. Lett. 2006 14 1378.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 1378
-
-
Ishida, J.1
Yamamoto, H.2
Kido, Y.3
Kamijo, K.4
Murano, K.5
Miyake, H.6
Ohkubo, M.7
Kinoshita, T.8
Warizaya, M.9
Iwashita, A.10
Mihara, K.11
Matsuoka, N.12
Hattori, K.13
-
57
-
-
0037363116
-
-
For the reviews on silica Lewis acid mediated reaction and selected examples of TMSCl promoted organic conversions, see
-
For the reviews on silica Lewis acid mediated reaction and selected examples of TMSCl promoted organic conversions, see A. D. Dilman S. L. Ioffe Chem. Rev. 2003 103 733.
-
(2003)
Chem. Rev.
, vol.103
, pp. 733
-
-
Dilman, A.D.1
Ioffe, S.L.2
-
68
-
-
0037167077
-
-
For the synthesis and characterizaition of Shiff base 5, see
-
For the synthesis and characterizaition of Shiff base 5, see D. M. Boghaei S. Mohebi Tetrahedron 2002 58 5357.
-
(2002)
Tetrahedron
, vol.58
, pp. 5357
-
-
Boghaei, D.M.1
Mohebi, S.2
|