A
Attaluri R. Prasad
Researcher at Indian Institute of Chemical Technology
Publications - 64
Citations - 1408
Attaluri R. Prasad is an academic researcher from Indian Institute of Chemical Technology. The author has contributed to research in topics: Total synthesis & Catalysis. The author has an hindex of 20, co-authored 64 publications receiving 1328 citations. Previous affiliations of Attaluri R. Prasad include Council of Scientific and Industrial Research.
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Sulfamic acid: an efficient, cost-effective and recyclable solid acid catalyst for the Friedlander quinoline synthesis
Jhillu S. Yadav,P. Purushothama Rao,D. Sreenu,R. Srinivasa Rao,V. Naveen Kumar,Kommu Nagaiah,Attaluri R. Prasad +6 more
TL;DR: In this paper, Amino-aryl ketones undergo smooth condensation with α-methylene ketones in the presence of sulfamic acid (NH2SO3H) under mild reaction conditions to afford the corresponding polysubstituted quinolines in excellent yields.
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Ultrasound-accelerated synthesis of 3,4-dihydropyrimidin-2(1H)-ones with ceric ammonium nitrate
Jhillu S. Yadav,Basi V. Subba Reddy,Kasireddy Bhaskar Reddy,Kavuda Sarita Raj,Attaluri R. Prasad +4 more
TL;DR: Ceric ammonium nitrate efficiently catalyzes the three component condensation of an aldehyde, β-ketoester and urea in methanol to afford the corresponding dihydropyrimidinones in excellent yields under sonication as discussed by the authors.
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Glaser oxidative coupling in ionic liquids: an improved synthesis of conjugated 1,3-diynes
TL;DR: Terminal alkynes undergo oxidative-coupling smoothly in the presence of the CuCl-TMEDA catalytic system in hydrophobic [bmim]PF6 ionic liquid under aerobic conditions to produce 1,3-diynes in excellent yields under mild conditions.
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Iodine as novel reagent for the 1,2-addition of trimethylsilyl cyanide to ketones including α,β-unsaturated ketones
TL;DR: In this paper, the addition of trimethylsilyl cyanide to a range of simple and functionalized ketones under very mild and convenient conditions to afford the corresponding cyanohydrin trimethyl silyl ethers in excellent yields in a short reaction period with high selectivity.
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Lewis Acidic Chloroaluminate Ionic Liquids: Novel Reaction Media for the Synthesis of 4‐Chloropyrans
TL;DR: In this article, the ionic liquid plays a dual role as both catalyst and solvent, providing a rapid and efficient route to the synthesis of chlorotetrahydropyrans.