B. Rajitha
National Institute of Technology, Warangal
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Featured researches published by B. Rajitha.
Synthetic Communications | 2008
Y. Thirupathi Reddy; Vijayakumar N. Sonar; Peter A. Crooks; Pavan K. Dasari; P. Narsimha Reddy; B. Rajitha
Abstract An efficient and convenient method for the synthesis of substituted coumarins via Pechmann condensation of different phenols with ethylacetoacetate in the presence of ammonium cerium(IV) nitrate as the catalyst in a solvent- free media using both conventional heating and microwave irradiation.
Phosphorus Sulfur and Silicon and The Related Elements | 2007
Y. Thirupathi Reddy; P. Narsimha Reddy; B. Sunil Kumar; Pradeep Rajput; N. Sreenivasulu; B. Rajitha
α-Aminophosphonates are synthesized by three-component condensation of aldehydes, amines, and trimethylphosphite in acetonitrile by using TiCl4 as catalyst. Compared to conventional methods, this new method consistently has advantages, including excellent yields, short reaction times, and mild reaction conditions.
Russian Journal of Organic Chemistry | 2006
B. Sunil Kumar; N. Srinivasulu; R. H. Udupi; B. Rajitha; Y. Thirupathi Reddy; P. Narsimha Reddy; P. S. Kumar
A convenient procedure is reported for the synthesis of benzo[g]-and benzo[h]chromene derivatives via one-pot three-component condensation of aromatic aldehydes with malononitrile or ethyl cyanoacetate and 1-or 2-naphthol in the presence of 10 mol % of titanium tetrachloride as catalyst. The reactions require no solvent; they are characterized by simple experimental procedure and easy isolation and can be performed on enlarged scale.
Synthetic Communications | 2012
B. Suresh Kuarm; B. Rajitha
Abstract A simple and efficient method has been developed for the synthesis of 4,4′-(arylmethylene)bis(1H-pyrazol-5-ols) by the condensation reaction between substituted aldehydes, and 1-phenyl-3-methylpyrazol-5-one in the presence of xanthan sulfuric acid (XSA) as a solid acid catalyst. This method is simple and cost-effective with short reaction times. Yields are excellent with high purity, and the catalyst could be easily recycled. GRAPHICAL ABSTRACT
Medicinal Chemistry Research | 2013
S. Vijaya Laxmi; B. Suresh Kuarm; B. Rajitha
A series of 5-((3-(2-oxo-2H-chromen-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-trione (4a–f) and dihydro-5-((3-(2-oxo-2H-chromen-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene)-2-thioxopyrimidine-4,6(1H,5H)-dione (5a–f) derivatives were synthesized by the condensation of 3-(2-oxo2H-chromen-3-yl)-1-phenyl-1H-pyrazole-4-carbaldehyde (3a–f) with barbituric acid and thiobarbituric acid in acetic acid under microwave irradiation method. The newly synthesized compounds were evaluated for their antibacterial activity against Bcillus subtilis, Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Pseudomonas aeoginosa, and Klebsiella pneumoniae. All the compounds were found to be moderately active against used microorganisms, whereas compounds (4d) and (4e) exhibited good antifungal activity against Aspergillus niger.
Synthetic Communications | 2010
B. Suresh Kuarm; J. Venu Madhav; S. Vijaya Laxmi; B. Rajitha; Y. Thirupathi Reddy; P. Narsimha Reddy; Peter A. Crooks
A facile synthesis of coumarins was performed in excellent yields via Pechmann condensation by using different type of phenols and ethylacetoacetates under solvent–free media using both conventional method and microwave irradiation in short reaction times is described. The reaction workup is very simple, and the catalyst can be easily separated from the reaction mixture and reused several times in subsequent reactions.
Chemistry of Heterocyclic Compounds | 2006
B. Sunil Kumar; P. S. Kumar; N. Srinivasulu; B. Rajitha; Y. Thirupathi Reddy; P. Narsimha Reddy; R. H. Udupi
Good yields of substituted coumarins were obtained by a synthetic method involving the Pechmann reaction using vanadium(III)chloride (VCl3) reagent to effect this condensation under solvent-free conditions.
Synthetic Communications | 2011
B. Suresh Kuarm; J. Venu Madhav; S. Vijaya Laxmi; B. Rajitha; Y. Thirupathi Reddy; P. Narsimha Reddy; Peter A. Crooks
Abstract A series of 1-oxo-hexahydroxanthene derivatives was synthesized at room temperature in solid state from substituted salicylaldehydes and substituted 1,3-hexanediones in the presence of a catalytic amount of cellulose sulfuric acid. The results showed that the reaction performed under solid-state conditions was benign to the environment, with higher yields and more convenient workup.
Synthetic Communications | 2008
J. Venu Madhav; B. Suresh Kuarm; P. Someshwar; B. Rajitha; Y. Thirupathi Reddy; Peter A. Crooks
Abstract CuPy2Cl2 is an efficient catalyst for the preparation of propargylamines via three-component coupling reaction of aromatic aldehydes, amines, and aromatic alkynes stirred at 95 °C without using any solvent to afford the corresponding products in good yields. The reaction mixture was irradiated at 450 W in a microwave oven to furnish the expected products in excellent yields.
Synthetic Communications | 2011
B. Suresh Kuarm; J. Venu Madhav; B. Rajitha; Y. Thirupathi Reddy; P. Narsimha Reddy; Peter A. Crooks
Abstract An efficient method for the synthesis of 2-substituted benzimidazoles has been developed. In this method, benzo[c][1,2,5]thiadiazole-4,5-diamine was condensed with different aldehydes in the presence of cellulose sulfuric acid under solvent-free conditions by simple physical grinding of reactants using a mortar and pestle at room temperature. The methodology is mild, high-yielding, and green, and the catalyst could be easily recycled.