scholarly journals THE ALDOL CONDENSATION WITH 2,3-DIPHENYL-4-THIAZOLIDINONE

1963 ◽  
Vol 41 (4) ◽  
pp. 817-820 ◽  
Author(s):  
Frances C. Brown ◽  
R. Sidney Jones ◽  
Mildred Kent

The aldol condensation between 2,3-diphenyl-4-thiazolidinone and aromatic aldehydes, which cannot be effected by the usual catalysts used in the analogous reactions of 2-thiono-, 2-oxo-, and 2-imino-4-thiazolidinones, was achieved by the use of ethoxide ion. The structure of the 2,3-diphenyl-5-arylidene-4-thiazolidinone was confirmed by ultraviolet spectral data.

Author(s):  
B. Shiva kumar ◽  
Navnath V. Kalyane ◽  
B. Shivaram Krishna ◽  
B. Shireesha ◽  
V. M. Reddy

Three different 3-amino-2-mercaptoquinazolin-4(3H)-ones were prepared from the substituted anthranilic acids. Likewise four different chalcones were also prepared by mixed aldol condensation of four aromatic aldehydes with acetophenone. Each of the 3-amino, 2-mercapto quinazolinones was subjected to a cycloaddition reaction with chalcones, separately by heating under reflux in acetic anhydride. The product obtained in each case has been purified and characterized as the respective 2-aryl-3,4-dihydro-4-oxoquinazolin-[2,3-b]-2,3-dihydro-4-phenyl –1,3,4-thiadiazepine on the basis of  their analytical and spectral data.             These new fused thiadiazepines were evaluated for their locomotor, anti psychotic and muscle relaxant activities by standard methods using animal models and compared with that of standard employed


2009 ◽  
Vol 6 (3) ◽  
pp. 866-870
Author(s):  
CH. Sridevi ◽  
K. Balaji ◽  
A. Naidu ◽  
R. Sudhakaran

2,3-Diphenyl quinoxaline(SI)was fused with 2-amino benzothiazoles(SII)by a methylene bridge, which was then allowed for acetylation. The acetylated product (SIV) was made to react with different aromatic aldehydes to give chalcones(SV1-SV5). Chalcones refluxed with substituted acid hydrazides to afford different phenyl pyrazolo benzothiazolo quinoxaline derivatives(SVI1-SVI15). The structure of chalcones and phenyl pyrazolo benzothiazolo quinoxaline derivatives were confirmed by M.P, TLC and spectral data. All the synthesized compounds were screened for their antimicrobial activities.


Author(s):  
Fengan Han ◽  
Jingyuan Xu ◽  
Guangyi Li ◽  
Jilei Xu ◽  
Aiqin Wang ◽  
...  

High-density and low freezing point dicycloalkanes were synthesized by the aldol condensation of methyl isobutyl ketone with aromatic aldehydes followed by hydrodeoxygenation under solvent-free conditions.


ChemInform ◽  
2005 ◽  
Vol 36 (3) ◽  
Author(s):  
S. Z. Vatsadze ◽  
V. N. Nuriev ◽  
I. F. Leshcheva ◽  
N. V. Zyk

2010 ◽  
Vol 7 (2) ◽  
pp. 433-436 ◽  
Author(s):  
B. Ramesh ◽  
B. Someswara Rao

Some new chalcones have been synthesized by the condensation of 2-acetyl thiophene with various aromatic aldehydes in 40% alkali. The synthesized compounds were identified by spectral data and screened for anti-inflammatory activity. Some of these compounds showed moderate to considerable anti-inflammatory activity.


Drug Research ◽  
2018 ◽  
Vol 69 (08) ◽  
pp. 445-450 ◽  
Author(s):  
Sachin Saini ◽  

Abstract2-Amino-5-(3’-indolomethylene)-1, 3 , 4 - oxadiazole (3) undergoes facile condensation with various aromatic aldehydes to gave 2-substitiuted arylidenylamino-5-(3’- indolomethylene) – 1, 3 , 4 – oxadiazole (4–8). Cyclocondensation of (4–8) with thioglycolic acid and triethylamine yielded 3-[5’-(3”- indolomethylene)- 1’, 3’, 4’- oxadiazol-2’-yl]- 2- (substituted aryl)-4- thiazolidinones (9–13) and 1-[5’-(3”- indolomethylene) -1’, 3’, 4’- oxadiazol - 2’- yl ] -4-(substituted aryl) -2- azetidinones (14–18). The structures of these compounds were established on the basis of analytical and spectral data. The newly synthesised compounds were evaluated for their anticonvulsant activity and acute toxicity.


2014 ◽  
Vol 44 (9) ◽  
pp. 1245-1250 ◽  
Author(s):  
Val V. Martichonok ◽  
Peter K. Chiang ◽  
Padraick J. Dornbush ◽  
Kirkwood M. Land

2005 ◽  
Vol 2 (2) ◽  
pp. 109-112
Author(s):  
A. K. Parekh ◽  
K. K. Desai

Some new chalcones have been prepared by Claisen-schmidt condensation of ketone and different aromatic aldehydes. These chalcones on condensation with urea in presence of acid gave Pyrimidine-2-ones. The synthesized compounds have been characterized by elemental analysis, IR and1H NMR spectral data. They have been screened for their antibacterial activity against Gram positive bacteria B. subtillis & S. aureus and Gram negative bacteria E. coli & S. typhi.


Sign in / Sign up

Export Citation Format

Share Document