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3
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Ito Y., Inubushi Y., Sugaya T., Kobayashi K., and Saegusa T. Bull. Chem. Soc. Jpn. 51 (1978) 1186
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Ito, Y.1
Inubushi, Y.2
Sugaya, T.3
Kobayashi, K.4
Saegusa, T.5
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4
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62549105379
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For recent reports on the biological activity of indole-3-carboxylates
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For recent reports on the biological activity of indole-3-carboxylates:
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7
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62549118757
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Indole-3-carboxylates have recently utilized for the synthesis of more complex molecules
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Indole-3-carboxylates have recently utilized for the synthesis of more complex molecules:
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8
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21144450350
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Hopkins C.R., Czekaj M., Kaye S., Gao Z., Pribish J., Pauls H., Liang G., Sides K., Cramer D., Cairns K., Luo Y., Lim H.-K., Vaz R., Rebello S., Maignan S., Dupuy A., Mathieu M., and Levell J. Bioorg. Med. Chem. Lett. 15 (2005) 2734
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Hopkins, C.R.1
Czekaj, M.2
Kaye, S.3
Gao, Z.4
Pribish, J.5
Pauls, H.6
Liang, G.7
Sides, K.8
Cramer, D.9
Cairns, K.10
Luo, Y.11
Lim, H.-K.12
Vaz, R.13
Rebello, S.14
Maignan, S.15
Dupuy, A.16
Mathieu, M.17
Levell, J.18
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9
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62549144481
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For recent syntheses of indole-3-carboxylates
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For recent syntheses of indole-3-carboxylates:
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13
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0018385643
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Using Nenitzescu reaction;
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Using Nenitzescu reaction;. Kuckländer U. Arch. Pharm. 312 (1979) 515
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(1979)
Arch. Pharm.
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Kuckländer, U.1
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14
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33846120947
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Via PIFA-mediated intramolecular cyclization of 2-aryl-3-arylaminoacrylates:
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Via PIFA-mediated intramolecular cyclization of 2-aryl-3-arylaminoacrylates:. Du Y., Liu R., Linn G., and Zhao K. Org. Lett. 8 (2006) 5919
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(2006)
Org. Lett.
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Du, Y.1
Liu, R.2
Linn, G.3
Zhao, K.4
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15
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34748921166
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Via a reaction of N,N-diphenylhydrazine with diethyl acetylenedicarboxylate:
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Via a reaction of N,N-diphenylhydrazine with diethyl acetylenedicarboxylate:. Sayyed I.A., Alex K., Tillack A., Schwarz N., Michalik D., and Beller M. Eur. J. Org. Chem. (2007) 4525
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(2007)
Eur. J. Org. Chem.
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Sayyed, I.A.1
Alex, K.2
Tillack, A.3
Schwarz, N.4
Michalik, D.5
Beller, M.6
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16
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44949150209
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Via a copper-catalyzed reaction of methyl 2-(2-bromophenyl)acetate with methyl formate and arylamines:
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Via a copper-catalyzed reaction of methyl 2-(2-bromophenyl)acetate with methyl formate and arylamines:. Melkonyan R.S., Karchava A.V., and Yurovskaya A. J. Org. Chem. 73 (2008) 4275
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Melkonyan, R.S.1
Karchava, A.V.2
Yurovskaya, A.3
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19
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62549107128
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N-4-Nitrophenylation of indole with 4-iodonitrobenzene has been achieved using copper catalysts at higher temperatures 90-160 °C
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N-4-Nitrophenylation of indole with 4-iodonitrobenzene has been achieved using copper catalysts at higher temperatures (90-160 °C):
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22
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0038391514
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1-(2-Nitrophenyl)- and 1-(2,4-dinitrophenyl)indoles have been prepared by N-arylation of indoline-2-carboxylic acid followed by decarboxylation and dehydrogenation;
-
1-(2-Nitrophenyl)- and 1-(2,4-dinitrophenyl)indoles have been prepared by N-arylation of indoline-2-carboxylic acid followed by decarboxylation and dehydrogenation;. Chicharro R., de Castro S., Reino J.L., and Aran V.J. Eur. J. Org. Chem. (2003) 2314
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(2003)
Eur. J. Org. Chem.
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Chicharro, R.1
de Castro, S.2
Reino, J.L.3
Aran, V.J.4
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