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Rajendra P. Pawar

Researcher at Hebrew University of Jerusalem

Publications -  175
Citations -  2436

Rajendra P. Pawar is an academic researcher from Hebrew University of Jerusalem. The author has contributed to research in topics: Catalysis & Ionic liquid. The author has an hindex of 22, co-authored 170 publications receiving 1917 citations. Previous affiliations of Rajendra P. Pawar include Swami Ramanand Teerth Marathwada University.

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Green and efficient synthesis of pyranopyrazoles catalyzed by ammoniumchloride in water

TL;DR: A green and efficient ammonium chloride catalyzed four component condensation of aldehyde, malononitrile, hydrazine hydrate and ethyl acetoacetate in aqueous medium as mentioned in this paper.
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Iodine and Iodic Acid: An Efficient Reagent Combination for Iodination of Aryl Hydroxy Ketones.

TL;DR: A variety of ortho-hydroxy substituted aromatic carbonyl compounds were regioselectively iodized with iodine and iodic acid in excellent yields as discussed by the authors, and they were used in a variety of applications.
Journal Article

FACILE AND EFFICIENT METHOD FOR PREPARATION OF SCHIFF BASES CATALYZED BY Ni (NO3)2.6H2O UNDER ROOM TEMPERATURE

TL;DR: In this paper, some Schiff bases were prepared with help of aromatic primary amines and highly substituted aromatic aldehydes in methanol and in presence of Ni (NO3)2.6H2O as catalyst at room temperature.
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A one pot three-component synthesis of spirooxoindoles using Cu-nanoparticles grafted on carbon microspheres as catalyst

TL;DR: In this paper, the copper nanoparticles grafted on carbon microsphere are employed for an efficient one-pot three-component synthesis of spirooxoindole derivatives involving isatin, malononitrile and enolizable ketones.
Proceedings ArticleDOI

Nano‐particulate Aluminium Nitride/Al: An Efficient and Versatile Heterogeneous Catalyst for the Synthesis of Biginelli Scaffolds

TL;DR: In this paper, a new heterogeneous solid acid catalyst for the synthesis of 3, 4, dihydroxypyrimidi•2−(1H)ones and their sulphur analogues using the Biginelli reaction is presented.