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Iadeishisha Kharbangar

Researcher at North Eastern Hill University

Publications -  10
Citations -  274

Iadeishisha Kharbangar is an academic researcher from North Eastern Hill University. The author has contributed to research in topics: Regioselectivity & Catalysis. The author has an hindex of 6, co-authored 9 publications receiving 248 citations.

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l-Proline as an efficicent catalyst for the multi-component synthesis of 6-amino-4-alkyl/aryl-3-methyl-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitriles in water

TL;DR: In this article, an efficient four-component synthesis of 6-amino-4-alkyl/aryl-3-methyl-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitriles involving ethyl acetoacetate, hydrazine hydrate, malononitrile, and various aldehydes using l -proline (10 ǫ%) in water under mild reaction condition in excellent yields is established.
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Synthetic Developments in Functionalized Pyrano[2,3-c]pyrazoles. A Review

TL;DR: The pyran ring and its derivatives have been and continue to be a subject of considerable importance due to their wide spectrum of biological applications as mentioned in this paper, and they have been used in many applications.
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Reaction of Selenium Dioxide with Aromatic Ketones in the Presence of Boron Triflouride Etherate: A Protocol for the Synthesis of Triarylethanones

TL;DR: An efficient regioselective protocol for the C-C bond formation by the unexpected α,α-diarylation of aromatic ketones with unactivated arenes in the presence of selenium dioxide and boron trifluoride etherate has been developed.
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One‐Pot Synthesis of Unsymmetrical Benzils by Oxidative Coupling Using Selenium Dioxide and p‐Toluenesulfonic Acid Monohydrate

TL;DR: In this paper, the α-carbon atom of aromatic ketones with unactivated arenes in the presence of selenium dioxide and p-toluenesulfonic acid monohydrate is described.
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KF-Al 2 O 3 as an Efficient and Recyclable Basic Catalyst for the Synthesis of 4 H -Pyran-3-carboxylates and 5-Acetyl-4 H -pyrans

TL;DR: In this paper, the basic catalyst for the three-component synthesis of 4H-pyran derivatives by the reaction of aldehydes, malononitrile and active methylene dicarbonyl compounds in ethanol at room temperature is described.