3 (3,4 DIMETHOXYPHENYL) N (4 METHYL 1,3 BENZOTHIAZOL 2 YL)ACRYLAMIDE;
3 (3,4 DIMETHOXYPHENYL) N (6 ETHOXY 1,3 BENZOTHIAZOL 2 YL)ACRYLAMIDE;
3 (3,4 DIMETHOXYPHENYL) N (6 METHOXY 1,3 BENZOTHIAZOL 2 YL)ACRYLAMIDE;
3 (3,4 DIMETHOXYPHENYL) N (6 METHYL 1,3 BENZOTHIAZOL 2 YL)ACRYLAMIDE;
3 (3,4 DIMETHOXYPHENYL) N (6 METHYLPYRIDIN 2 YL)ACRYLAMIDE;
3 (3,4 DIMETHOXYPHENYL) N (6 NITRO 1,3 BENZOTHIAZOL 2 YL)ACRYLAMIDE;
3 (3,4 DIMETHOXYPHENYL) N 1,3 THIAZOL 2 YLACRYLAMIDE;
3 (3,4 DIMETHOXYPHENYL) N [6 (METHYLSULFONYL) 1,3 BENZOTHIAZOL 2 YL]ACRYLAMIDE;
3 (3,4 DIMETHOXYPHENYL) N PYRIDIN 2 YLACRYLAMIDE;
3 PHENYL N 1,3 THIAZOL 2 YLACRYLAMIDE;
AMIDE;
CINNAMIC ACID DERIVATIVE;
N (4 CHLORO 1,3 BENZOTHIAZOL 2 YL) 3 (3,4 DIMETHOXYPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 (2 CHLOROPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 (2,5 DIMETHOXYPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 (3,4 DIMETHOXYPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 (4 BUTOXYPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 (4 CHLOROPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 (4 ETHOXYPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 (4 ETHYLPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 (4 METHOXYPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 (4 METHYLPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 (4 PROPOXYPHENYL)ACRYLAMIDE;
N 1,3 BENZOTHIAZOL 2 YL 3 PHENYLACRYLAMIDE;
N,3 DIPHENYLACRYLAMIDE;
UNCLASSIFIED DRUG;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
DRUG STRUCTURE;
ENERGY TRANSFER;
MICROWAVE IRRADIATION;
ONE POT SYNTHESIS;
PROTON NUCLEAR MAGNETIC RESONANCE;
REACTION TIME;
Synthesis of cinnamic acid derivatives and their inhibitory effects on LDL-oxidation, acyl-CoA:cholesterol acyltransferase-1 and -2 activity, and decrease of HDL-particle size
DOI 10.1016/j.bmcl.2004.06.101, PII S0960894X04008947
Lee, S.; Han, J. M.; Kim, H.; Kim, E.; Jeong, T. S.; Lee, W. S.; Cho, K. H. Synthesis of cinnamic acid derivatives and their inhibitory effects on LDL-oxidation, acyl-CoA: cholesterol acyltransferase-1 and-2 activity, and decrease of HDL-particle size. Bioorg. Med. Chem. Lett. 2004, 14 (18), 4677-4681. (Pubitemid 39490288)
Vitro effect of a new cinnamic acid derivative against the epimastigote form of Tripanosoma cruzi
Pardo, G. L.; Inada, N. M.; Pello? n, R. F.; Docampo, M. L.; Fascio, M. L.; D' Accorso, N. B.; Vercesi, A. E. In vitro effect of a new cinnamic acid derivative against the epimastigote form of Tripanosoma cruzi. Arzneimittelforschung 2009, 59 (4), 207-211.
Structure-activity relationships of novel anti-malarial agents. Part 7: N-(3-benzoyl-4-tolylacetylaminophenyl)-3-(5-aryl-2-furyl)acrylic acid amides with polar moieties
DOI 10.1016/S0960-894X(03)00353-6
Wiesner, J.; Mitsch, A.; Jomaa, H.; Schlitzer, M. Structure-activity relationships of novel anti-malarial agents, part 7: N-(3-Benzoyl-4- tolylacetylaminophenyl)-3-(5-aryl-2-furyl)acrylic acid amides with polar moieties. Bioorg. Med. Chem. Lett. 2003, 13, 2159-2161. (Pubitemid 36694296)
Cinnamoyland hydroxycinnamoyl amides of glaucine and their biological activity
Spasova, M.; Philipov, S.; Nikolaeva-Glomb, L.; Galabov, A.; Milkova, T. Cinnamoyland hydroxycinnamoyl amides of glaucine and their biological activity. Bioorg. Med. Chem. 2008, 16, 7457-7461.
Mild method for Ullmann reaction of 2-chlorobenzoic acids and aminothiazoles or aminobenzothiazoles under ultrasonic irradiation
DOI 10.1080/00397910701319056, PII 779480795
Pellon, R. F.; Docampo, M.; Fascio, M. Mild method for Ullmann reaction of 2-chlorobenzoic acids and aminothiazoles or aminobenzothiazoles under ultrasonic irradiation. Synth. Commun. 2007, 37 (11), 1853-1864; (Pubitemid 46911868)
Ultrasound-promoted reaction of 2-chlorobenzoic acids and aliphatic amines
(b) Docampo, M.; Pellón, R. F.; Estevez-Braun, A. G.; Ravelo, A. Ultrasound-promoted reaction of 2-chlorobenzoic acids and aliphatic amines. Eur. J. Org. Chem. 2007, 24, 4111-4115;
Microwave-assisted synthesis of 2-phenoxybenzoic acids
(c) Pellón, R. F.; Martín, A.; Mesa, M.; Docampo, M. L.; Gómez, V. Microwave-assisted synthesis of 2-phenoxybenzoic acids. J. Chem. Res. Synop. 2006, 8, 527-529; (Pubitemid 44421860)
Fast synthesis of substituted N-phenylanthranilic acids using Ullmann condensation under microwave irradiation in dry media
DOI 10.1080/00397910500374955, PII TL25375115121153
(d) Martín, A.; Mesa, M.; Docampo, M. L.; Gómez, V.; Pellón, R. F. Fast synthesis of substituted N-phenylanthranilic acids using Ullmann condensation under microwave irradiation in dry media. Synth. Commun. 2006, 36 (3), 271-277. (Pubitemid 43162284)
Thermal and microwave-assisted rapid synthesis of substituted imidazo[1,2-A]pyridines under solvent-and catalyst-free conditions
Chunavala, K. C.; Joshi, G.; Suresh, E.; Adimurthy, S. Thermal and microwave-assisted rapid synthesis of substituted imidazo[1,2-a]pyridines under solvent-and catalyst-free conditions. Synthesis 2011, 4, 635-641.
Microwave-promoted Ullmann condensation of 2-aminopyridines with 2-chlorobenzoic acids
Pellon, R. F.; Martin, A.; Docampo, M.; Mesa, M. Microwave-promoted Ullmann condensation of 2-aminopyridines with 2-chlorobenzoic acids. Synth. Commun. 2006, 36 (6), 1715-1719.