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Kommu Nagaiah

Researcher at Indian Institute of Chemical Technology

Publications -  101
Citations -  2013

Kommu Nagaiah is an academic researcher from Indian Institute of Chemical Technology. The author has contributed to research in topics: Catalysis & Ionic liquid. The author has an hindex of 23, co-authored 100 publications receiving 1846 citations. Previous affiliations of Kommu Nagaiah include Academy of Scientific and Innovative Research.

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Phosphane‐Catalyzed Knoevenagel Condensation: A Facile Synthesis of α‐Cyanoacrylates and α‐Cyanoacrylonitriles

TL;DR: In this paper, Triphenylphosphane (TPP) was used as a novel and efficient catalyst for the Knoevenagel condensation of aldehydes with acidic methylene compounds such as ethyl cyanoacetate and malononitrile to afford substituted olefins.
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Sulfamic acid: an efficient, cost-effective and recyclable solid acid catalyst for the Friedlander quinoline synthesis

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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Green Protocol for the Biginelli Three-Component Reaction: Ag3PW12O40 as a Novel, Water-Tolerant Heteropolyacid for the Synthesis of 3,4-Dihydropyrimidinones

TL;DR: In this paper, a three-component condensation of an aldehyde, β-keto ester, and urea proceeds smoothly on the surface of the silver salt of heteropolyacid (HPA), i.e. Ag3PW12O40, in water to afford the corresponding 3,4-dihydropyrimidinones in high-to-quantitative yields under mild conditions.
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A Novel L-Proline Catalyzed Biginelli Reaction : One-Pot Synthesis of 3, 4-Dihydropyrimidin-2(1H)-ones under Solvent-Free Conditions

TL;DR: In this paper, an efficient and simple protocol for the Biginelli reaction has been developed for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones in a one-pot three-component condensation of aldeh...
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An Efficient Knoevenagel Condensation Catalyzed by LaCl3.7H2O in Heterogeneous Medium

TL;DR: In this article, the authors performed Knoevenagel condensation in absence of solvent with a mild Lewis acid Lanthanum(III) chloride, to prepare substituted alkenes.