-
1
-
-
30344457007
-
Microwave-assisted synthesis of N-alkylated benzotriazole derivatives: Antimicrobial studies
-
Swamy, S. N.; Basappa; Sarala, G.; Priya, B. S.; Gaonkar, S. L.; Prasad, J. S.; Rangappa, K. S. Microwave-assisted synthesis of N-alkylated benzotriazole derivatives: Antimicrobial studies. Bioorg. Med. Chem. Lett. 2006, 16, 999-1004.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 999-1004
-
-
Swamy, S.N.1
Basappa2
Sarala, G.3
Priya, B.S.4
Gaonkar, S.L.5
Prasad, J.S.6
Rangappa, K.S.7
-
2
-
-
0000777566
-
Phase-transfer alkylation of heterocycles in the presence of 18-crown-6 and potassium tert-butoxide
-
Guida, W. C.; Mathre, D. J. Phase-transfer alkylation of heterocycles in the presence of 18-crown-6 and potassium tert-butoxide. J. Org. Chem. 1980, 16, 3172-3176.
-
(1980)
J. Org. Chem.
, vol.16
, pp. 3172-3176
-
-
Guida, W.C.1
Mathre, D.J.2
-
3
-
-
0019995418
-
Biotransformation von 1H-Benzotriazol und N-1-Alkylbenzo-triazolen in vitro
-
Hoffmann, H.; Pooth, R. Biotransformation von 1H-Benzotriazol und N-1-Alkylbenzo-triazolen in vitro. Arch. Pharm. 1982, 315, 422-428.
-
(1982)
Arch. Pharm.
, vol.315
, pp. 422-428
-
-
Hoffmann, H.1
Pooth, R.2
-
4
-
-
0001512640
-
N-Alkylation of benzimidazoles and benzotriazole via phase-transfer catalysis
-
Mathias, L. J.; Burkett, D. N-Alkylation of benzimidazoles and benzotriazole via phase-transfer catalysis. Tetrahedron Lett. 1979, 20, 4709-4712.
-
(1979)
Tetrahedron Lett.
, vol.20
, pp. 4709-4712
-
-
Mathias, L.J.1
Burkett, D.2
-
5
-
-
0001333118
-
N-Alkylation of pyrrole, indole, and several other nitrogen heterocycles using potassium hydroxide as a base in the presence of polyethylene glycols or their dialkyl ethers
-
Sukata, K. N-Alkylation of pyrrole, indole, and several other nitrogen heterocycles using potassium hydroxide as a base in the presence of polyethylene glycols or their dialkyl ethers. Bull. Chem. Soc. Jpn. 1983, 56, 280-284.
-
(1983)
Bull. Chem. Soc. Jpn.
, vol.56
, pp. 280-284
-
-
Sukata, K.1
-
6
-
-
3142616376
-
Organic reactions in ionic liquids: An efficient method for the N-alkylation of benzotriazole
-
Le, Z. G.; Chen, Z. C.; Hu, Y.; Zheng, Q. G. Organic reactions in ionic liquids: An efficient method for the N-alkylation of benzotriazole. J. Chem. Res. 2004, 2004, 344-346.
-
(2004)
J. Chem. Res.
, vol.2004
, pp. 344-346
-
-
Le, Z.G.1
Chen, Z.C.2
Hu, Y.3
Zheng, Q.G.4
-
7
-
-
84987177864
-
An improved method for the N-alkylation of benzotriazole and 1,2,4-triazole
-
Katritzky, A. R.; Kuzmierkiewicz, W.; Greenhill, J. V. An improved method for the N-alkylation of benzotriazole and 1,2,4-triazole. Reel. Trav. Chim. Pays-Bas. 1991, 110, 369-373.
-
(1991)
Reel. Trav. Chim. Pays-Bas.
, vol.110
, pp. 369-373
-
-
Katritzky, A.R.1
Kuzmierkiewicz, W.2
Greenhill, J.V.3
-
8
-
-
34548165276
-
Highly regioselective N-alkylation of benzotriazole under solvent-free conditions
-
Khalafi-Nezhad, A.; Zare, A.; Parhami, A.; Rad, M. N. S.; Nejabat, G. R. Highly regioselective N-alkylation of benzotriazole under solvent-free conditions. J. Iran. Chem. Soc. 2007, 4, 271-278.
-
(2007)
J. Iran. Chem. Soc.
, vol.4
, pp. 271-278
-
-
Khalafi-Nezhad, A.1
Zare, A.2
Parhami, A.3
Rad, M.N.S.4
Nejabat, G.R.5
-
9
-
-
53349118228
-
Quaternary ammonium salts as highly efficient and green alkylating agents for N-alkylation of azahe-terocycles under microwave irradiation
-
Khalafi-Nezhad, A.; Zare, A.; Parhami, A.; Hasaninejad, A.; Zarea, A. R. M. Quaternary ammonium salts as highly efficient and green alkylating agents for N-alkylation of azahe-terocycles under microwave irradiation. J. Iran. Chem. Soc. 2008, 5, S40-S46.
-
(2008)
J. Iran. Chem. Soc.
, vol.5
-
-
Khalafi-Nezhad, A.1
Zare, A.2
Parhami, A.3
Hasaninejad, A.4
Zarea, A.R.M.5
-
10
-
-
0009556551
-
Reactivity of azoles towards benzaldehyde and its dimethylacetal: Synthesis of N,N'-diazolylphenylmethanes
-
Ballesteros, P.; Elguero, J.; Claramunt, R. M. Reactivity of azoles towards benzaldehyde and its dimethylacetal: Synthesis of N,N'- diazolylphenylmethanes. Tetrahedron 1985, 41, 5955-5963.
-
(1985)
Tetrahedron
, vol.41
, pp. 5955-5963
-
-
Ballesteros, P.1
Elguero, J.2
Claramunt, R.M.3
-
11
-
-
0347417134
-
Room-temperature ionic liquids: Solvents for synthesis and catalysis
-
Welton, T. Room-temperature ionic liquids: Solvents for synthesis and catalysis. Chem. Rev. 1999, 99, 2071-2083. (Pubitemid 129585179)
-
(1999)
Chemical Reviews
, vol.99
, Issue.8
, pp. 2071-2083
-
-
Welton, T.1
-
12
-
-
61849132218
-
Ionic liquid as catalyst in the synthesis of N-alkyl trifluoromethyl pyrazoles
-
(a) Frizzo, C. P.; Moreira, D. N.; Guarda, E. A.; Fiss, G. F.; Marzari, M. R. B.; Zanatta, N.; Bonacorso, H. G.; Martins, M. A. P. Ionic liquid as catalyst in the synthesis of N-alkyl trifluoromethyl pyrazoles. Catal. Commun. 2009, 10, 1153-1156;
-
(2009)
Catal. Commun.
, vol.10
, pp. 1153-1156
-
-
Frizzo, C.P.1
Moreira, D.N.2
Guarda, E.A.3
Fiss, G.F.4
Marzari, M.R.B.5
Zanatta, N.6
Bonacorso, H.G.7
Martins, M.A.P.8
-
13
-
-
58149485193
-
Highly efficient procedure for the synthesis of biodiesel from soybean oil using chloroaluminate ionic liquid as catalyst
-
(b) Liang, X. Z.; Gong, G. Z.; Wu, H. H.; Yang, J. G. Highly efficient procedure for the synthesis of biodiesel from soybean oil using chloroaluminate ionic liquid as catalyst. Fuel 2009, 88, 603-616;
-
(2009)
Fuel
, vol.88
, pp. 603-616
-
-
Liang, X.Z.1
Gong, G.Z.2
Wu, H.H.3
Yang, J.G.4
-
14
-
-
40849140504
-
Ionic liquids in methyltrioxorhenium-catalyzed epoxidation-methanolysis of glycals under homogeneous and heterogeneous conditions
-
(c) Saladino, R.; Crestini, C.; Crucianelli, M.; Soldaini, G.; Cardona, F.; Goti, A. Ionic liquids in methyltrioxorhenium-catalyzed epoxidation- methanolysis of glycals under homogeneous and heterogeneous conditions. J. Mol. Catal. A: Chem. 2008, 284, 108-115;
-
(2008)
J. Mol. Catal. A: Chem.
, vol.284
, pp. 108-115
-
-
Saladino, R.1
Crestini, C.2
Crucianelli, M.3
Soldaini, G.4
Cardona, F.5
Goti, A.6
-
15
-
-
64649084297
-
Supported ionic liquid phase (SILP)-catalyzed hydroformylation of 1-butene in a gradient-free loop reactor
-
(d) Haumann, M.; Jakuttis, M.; Werner, S.; Wasserscheid, P. Supported ionic liquid phase (SILP)-catalyzed hydroformylation of 1-butene in a gradient-free loop reactor. J. Catal. 2009, 263, 321-327;
-
(2009)
J. Catal.
, vol.263
, pp. 321-327
-
-
Haumann, M.1
Jakuttis, M.2
Werner, S.3
Wasserscheid, P.4
-
16
-
-
40849095746
-
Catalysis by an ionic liquid: Highly efficient solvent-free synthesis of aryl-14H-dibenzo[a.j]xanthenes by molten tetrabutylammonium bromide under conventional and microwave heating
-
(e) Kantevari, S.; Chary, M. V.; Das, A. P. R.; Vuppalapatia, S. V. N.; Lingaiah, N. Catalysis by an ionic liquid: Highly efficient solvent-free synthesis of aryl-14H-dibenzo[a.j]xanthenes by molten tetrabutylammonium bromide under conventional and microwave heating. Catal. Commun. 2008, 9, 1575-1578.
-
(2008)
Catal. Commun.
, vol.9
, pp. 1575-1578
-
-
Kantevari, S.1
Chary, M.V.2
Das, A.P.R.3
Vuppalapatia, S.V.N.4
Lingaiah, N.5
-
17
-
-
56349111460
-
Synthesis of a basic imidazolide ionic liquid and its application in catalyzing Knoevenagel condensation
-
Chen, X.; Li, X.; Song, H.; Lü, Y.; Wang, F.; Hu, A. Synthesis of a basic imidazolide ionic liquid and its application in catalyzing Knoevenagel condensation. Chin. J. Catal. 2008, 29, 957-959.
-
(2008)
Chin. J. Catal.
, vol.29
, pp. 957-959
-
-
Chen, X.1
Li, X.2
Song, H.3
Lü, Y.4
Wang, F.5
Hu, A.6
-
18
-
-
58149344919
-
Catalytic amounts of Brønsted acidic ionic liquids promoted esterification: Study of acidity-activity relationship
-
(a)Zhao, Y. W.; Long, J. X.; Deng, F. G.; Liu, X. F.; Li, Z.; Xia, C. G.; Peng, J. J. Catalytic amounts of Brønsted acidic ionic liquids promoted esterification: Study of acidity-activity relationship. Catal. Commun. 2009, 10, 732-736;
-
(2009)
Catal. Commun.
, vol.10
, pp. 732-736
-
-
Zhao, Y.W.1
Long, J.X.2
Deng, F.G.3
Liu, X.F.4
Li, Z.5
Xia, C.G.6
Peng, J.J.7
-
19
-
-
59249093330
-
Brønsted acidic ionic liquid as an efficient and reusable catalyst for transesterification of b-ketoesters
-
(b) Qureshi, Z. S.; Deshmukh, K. M.; Bhor, M. D.; Bhanage, B. M. Brønsted acidic ionic liquid as an efficient and reusable catalyst for transesterification of b-ketoesters. Catal. Commun. 2009, 10, 833-837;
-
(2009)
Catal. Commun.
, vol.10
, pp. 833-837
-
-
Qureshi, Z.S.1
Deshmukh, K.M.2
Bhor, M.D.3
Bhanage, B.M.4
-
21
-
-
35648994821
-
A Brønsted acidic ionic liquid as an efficient and reusable catalyst system for esterification
-
(d) Zhang, H. B.; Xu, F.; Zhou, X. H.; Zhang, G. Y.; Wang, C. X. A Brønsted acidic ionic liquid as an efficient and reusable catalyst system for esterification. Green Chem. 2007, 9, 1208-1211.
-
(2007)
Green Chem.
, vol.9
, pp. 1208-1211
-
-
Zhang, H.B.1
Xu, F.2
Zhou, X.H.3
Zhang, G.Y.4
Wang, C.X.5
-
22
-
-
35649000027
-
Basic functionalized ionic liquid-catalyzed one-pot Mannich-type reaction: Three-component synthesis of b-amino carbonyl compounds
-
Gong, K.; Fang, D.; Wang, H. L.; Liu, Z. L. Basic functionalized ionic liquid-catalyzed one-pot Mannich-type reaction: Three-component synthesis of b-amino carbonyl compounds. Monatsh. Chem. 2007, 138, 1195-1198.
-
(2007)
Monatsh. Chem.
, vol.138
, pp. 1195-1198
-
-
Gong, K.1
Fang, D.2
Wang, H.L.3
Liu, Z.L.4
-
23
-
-
33748374224
-
Ionic liquid as catalyst and reaction medium: A simple, efficient, and green procedure for Knoevenagel condensation of aliphatic and aromatic carbonyl compounds using a task-specific basic ionic liquid
-
Ranu, B. C.; Jana, R. Ionic liquid as catalyst and reaction medium: A simple, efficient, and green procedure for Knoevenagel condensation of aliphatic and aromatic carbonyl compounds using a task-specific basic ionic liquid. Eur. J. Org. Chem. 2006, 3767-3770.
-
(2006)
Eur. J. Org. Chem.
, pp. 3767-3770
-
-
Ranu, B.C.1
Jana, R.2
-
24
-
-
35649016032
-
Application of basic ionic liquid [bmim]. OH to Knoevenagel and Perkin reactions
-
Li, J.; Sun, H.; Cai, X. C.; Dai, L. Y. Application of basic ionic liquid [bmim]OH to Knoevenagel and Perkin reactions. Chin. J. Org. Chem. 2007, 27, 1296-1299.
-
(2007)
Chin. J. Org. Chem.
, vol.27
, pp. 1296-1299
-
-
Li, J.1
Sun, H.2
Cai, X.C.3
Dai, L.Y.4
-
25
-
-
33646509010
-
Basic ionic liquid as catalysis and reaction medium: A novel and green protocol for the Markovnikov addition of N-heterocycles to vinyl esters, using a task-specific ionic liquid, [bmIm] OH
-
Xu, J. M.; Liu, B. K.; Wu, W. B.; Qian, C.; Wu, Q.; Lin, X. F. Basic ionic liquid as catalysis and reaction medium: A novel and green protocol for the Markovnikov addition of N-heterocycles to vinyl esters, using a task-specific ionic liquid, [bmIm]OH. J. Org. Chem. 2006, 71, 3991-3993.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 3991-3993
-
-
Xu, J.M.1
Liu, B.K.2
Wu, W.B.3
Qian, C.4
Wu, Q.5
Lin, X.F.6
-
26
-
-
33748957525
-
Highly efficient aza-Michael reactions of aromatic amines and N-heterocycles catalyzed by a basic ionic liquid under solvent-free conditions
-
(a) Yang, L.; Xu, L. W.; Zhou, W.; Li, L.; Xia, C. G. Highly efficient aza-Michael reactions of aromatic amines and N-heterocycles catalyzed by a basic ionic liquid under solvent-free conditions. Tetrahedron Lett. 2006, 47, 7723-7726;
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 7723-7726
-
-
Yang, L.1
Xu, L.W.2
Zhou, W.3
Li, L.4
Xia, C.G.5
-
27
-
-
33845323019
-
Ionic liquid as catalyst and solvent: The remarkable effect of a basic ionic liquid, [Bmim]OH, on Michael addition and alkylation of active methylene compounds
-
(b) Ranu, B. C.; Banerjee, S.; Jana, R. Ionic liquid as catalyst and solvent: The remarkable effect of a basic ionic liquid, [Bmim]OH, on Michael addition and alkylation of active methylene compounds. Tetrahedron 2007, 63, 776-782;
-
(2007)
Tetrahedron
, vol.63
, pp. 776-782
-
-
Ranu, B.C.1
Banerjee, S.2
Jana, R.3
-
28
-
-
34250685409
-
A basic ionic liquid as catalyst and reaction medium: A rapid and simple procedure for aza-Michael addition reactions
-
(c) Xu, J. M.; Wu, Q.; Zhang, Q. Y.; Zhang, F.; Lin, X. F. A basic ionic liquid as catalyst and reaction medium: A rapid and simple procedure for aza-Michael addition reactions. Eur. J. Org. Chem. 2007, 2007, 1798-1802;
-
(2007)
Eur. J. Org. Chem.
, vol.2007
, pp. 1798-1802
-
-
Xu, J.M.1
Wu, Q.2
Zhang, Q.Y.3
Zhang, F.4
Lin, X.F.5
-
29
-
-
33845444157
-
A fast and highly efficient protocol for Michael addition of N-heterocycles to a,b-unsaturated compound using basic ionic liquid [Bmim] OH as catalyst and green solvent
-
(d) Xu, J. M.; Qian, C.; Liu, B. K.; Wu, Q.; Lin, X. F. A fast and highly efficient protocol for Michael addition of N-heterocycles to a,b-unsaturated compound using basic ionic liquid [Bmim]OH as catalyst and green solvent. Tetrahedron 2007, 63, 986-990.
-
(2007)
Tetrahedron
, vol.63
, pp. 986-990
-
-
Xu, J.M.1
Qian, C.2
Liu, B.K.3
Wu, Q.4
Lin, X.F.5
-
30
-
-
45049088586
-
Ionic liquid-promoted interrupted Feist-Benary reaction with high diastereoselectivity
-
Ranu, B. C.; Adak, L.; Banerjee, S. Ionic liquid-promoted interrupted Feist-Benary reaction with high diastereoselectivity. Tetrahedron Lett. 2008, 49, 4613-4617.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 4613-4617
-
-
Ranu, B.C.1
Adak, L.2
Banerjee, S.3
-
31
-
-
50149105216
-
An efficient protocol for Henry reaction using basic ionic liquid [Bmim] OH as catalyst and reaction medium
-
(a) Wu, H.; Zhang, F. R.; Wan, Y.; Ye, L. An efficient protocol for Henry reaction using basic ionic liquid [Bmim]OH as catalyst and reaction medium. Lett. Org. Chem. 2008, 5, 209-211;
-
(2008)
Lett. Org. Chem.
, vol.5
, pp. 209-211
-
-
Wu, H.1
Zhang, F.R.2
Wan, Y.3
Ye, L.4
-
32
-
-
57749100966
-
The first ionic liquid-promoted, three-component coupling strategy for an expeditious synthesis of b-nitrocarbonitriles=thiocyanates
-
(b) Yadav, L. D. S.; Rai, A. The first ionic liquid-promoted, three-component coupling strategy for an expeditious synthesis of b-nitrocarbonitriles=thiocyanates. Tetrahedron Lett. 2009, 50, 640-643.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 640-643
-
-
Yadav, L.D.S.1
Rai, A.2
-
33
-
-
77955435582
-
A simple N-substitution of pyrrole and indole using basic ionic liquid [Bmim][OH] as catalyst and green solvent
-
Le, Z. G.; Zhong, T.; Xie, Z. B.; Xu, J. P. A simple N-substitution of pyrrole and indole using basic ionic liquid [Bmim][OH] as catalyst and green solvent. Heterocycles 2009, 78, 2013-2020.
-
(2009)
Heterocycles
, vol.78
, pp. 2013-2020
-
-
Le, Z.G.1
Zhong, T.2
Xie, Z.B.3
Xu, J.P.4
-
34
-
-
22244486653
-
Ionic liquid as catalyst and reaction medium: The dramatic influence of a task-specific ionic liquid, [Bmim] OH, in Michael addition of active methyl-ene compounds to conjugated ketones, carboxylic esters, and nitriles
-
Ranu, B. C.; Banerjee, S. Ionic liquid as catalyst and reaction medium: The dramatic influence of a task-specific ionic liquid, [Bmim]OH, in Michael addition of active methyl-ene compounds to conjugated ketones, carboxylic esters, and nitriles. Org. Lett. 2005, 7, 3049-3052.
-
(2005)
Org. Lett.
, vol.7
, pp. 3049-3052
-
-
Ranu, B.C.1
Banerjee, S.2
|