-
1
-
-
84890978162
-
-
For recent reviews of microwave-assisted synthesis, see: Ondruschka, B.; Bonrath, W.; Stuerga, D. Microwaves in Organic Synthesis, (2nd ed.) 2006, 1, 62.
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For recent reviews of microwave-assisted synthesis, see: Ondruschka, B.; Bonrath, W.; Stuerga, D. Microwaves in Organic Synthesis, (2nd ed.) 2006, 1, 62.
-
-
-
-
14
-
-
38949206341
-
-
Li J., Ye D., Liu H., Luo X., and Jiang H. Synth. Commun. 38 (2008) 567
-
(2008)
Synth. Commun.
, vol.38
, pp. 567
-
-
Li, J.1
Ye, D.2
Liu, H.3
Luo, X.4
Jiang, H.5
-
15
-
-
41649121875
-
-
Wei T.-B., Zhang Z.-R., Shi H.-X., Cui W.-H., and Zhang Y.-M. Youji Huaxue 28 (2008) 145
-
(2008)
Youji Huaxue
, vol.28
, pp. 145
-
-
Wei, T.-B.1
Zhang, Z.-R.2
Shi, H.-X.3
Cui, W.-H.4
Zhang, Y.-M.5
-
17
-
-
41649096530
-
-
Panunzio M., Bandini E., D'Aurizio A., Martelli G., Tamanini E., Xiao S.-Y., and Xia Z.-N. Youji Huaxue 28 (2008) 60
-
(2008)
Youji Huaxue
, vol.28
, pp. 60
-
-
Panunzio, M.1
Bandini, E.2
D'Aurizio, A.3
Martelli, G.4
Tamanini, E.5
Xiao, S.-Y.6
Xia, Z.-N.7
-
21
-
-
40849083663
-
-
de la Hoz A., Diaz-Ortiz A., Moreno A., Sanchez-Migallon A., Prieto P., Carrillo J.R., Vazquez E., Gomez M.V., and Herrero M.A. Comb. Chem. High Throughput Screening 10 (2007) 877
-
(2007)
Comb. Chem. High Throughput Screening
, vol.10
, pp. 877
-
-
de la Hoz, A.1
Diaz-Ortiz, A.2
Moreno, A.3
Sanchez-Migallon, A.4
Prieto, P.5
Carrillo, J.R.6
Vazquez, E.7
Gomez, M.V.8
Herrero, M.A.9
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26
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84890597202
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For reviews regarding multicomponent reactions, see:, Wiley-VCH, Weinheim, Germany
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For reviews regarding multicomponent reactions, see:. Zhu J., and Bie H. Multicomponent Reactions (2005), Wiley-VCH, Weinheim, Germany
-
(2005)
Multicomponent Reactions
-
-
Zhu, J.1
Bie, H.2
-
32
-
-
84868327332
-
-
Zhu J., and Bie H. (Eds), Wiley-VCH, Weinheim, Germany
-
Tietze L.F., and Rackelmann N. In: Zhu J., and Bie H. (Eds). Multicomponent Reactions (2005), Wiley-VCH, Weinheim, Germany 121-168
-
(2005)
Multicomponent Reactions
, pp. 121-168
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Tietze, L.F.1
Rackelmann, N.2
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34
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45649083266
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note
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Typical experimental procedure under microwave irradiation: Cyclic secondary amine (2.5 equiv) was treated with 4-fluorobenzaldehyde (1.24 mL, 11.6 mmol) and active methylidene (11.6 mmol) in EtOH (20 mL). The resulting mixture was placed into the microwave reactor for a specified reaction time. After the reaction was completed, the mixture was cooled down to rt and poured into 50 mL of water. Crude products were filtered off and purified by crystallization in EtOH.
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35
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0037219140
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For nucleophilic aromatic substitution of para-fluorobenzaldehde with cyclic amines, see:
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For nucleophilic aromatic substitution of para-fluorobenzaldehde with cyclic amines, see:. Mečiarová M., Toma S., Podlesná J., Kiripolský M., and Císařová I. Monatsh. Chem. 134 (2003) 37
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(2003)
Monatsh. Chem.
, vol.134
, pp. 37
-
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Mečiarová, M.1
Toma, S.2
Podlesná, J.3
Kiripolský, M.4
Císařová, I.5
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42
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84973022175
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The (E) geometry was determined by comparison with known compounds
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The (E) geometry was determined by comparison with known compounds. Shen Y., and Yang B. Synth. Commun. 19 (1989) 3069
-
(1989)
Synth. Commun.
, vol.19
, pp. 3069
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Shen, Y.1
Yang, B.2
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44
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45649084121
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note
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3). Then 5a (2.54 g, 11.6 mmol) was dissolved in EtOH (20 mL). The resulting solution was treated with cyclic secondary amine (2.5 equiv) and heated to reflux for 3 h. Then the mixture was cooled down to room temperature and poured into 50 mL of water. Crude products were filtered off and purified by crystallization in EtOH.
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