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D. Subhas Bose

Researcher at Indian Institute of Chemical Technology

Publications -  94
Citations -  1941

D. Subhas Bose is an academic researcher from Indian Institute of Chemical Technology. The author has contributed to research in topics: Catalysis & Primary (chemistry). The author has an hindex of 24, co-authored 94 publications receiving 1867 citations.

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Green Chemistry Approaches to the Synthesis of 5-Alkoxycarbonyl-4-aryl-3,4- dihydropyrimidin-2(1H)-ones by a Three-Component Coupling of One-Pot Condensation Reaction: Comparison of Ethanol, Water, and Solvent-free Conditions

TL;DR: This method provides an efficient and much improved modification of original Biginelli reaction reported in 1893, in terms of high yields, short reaction times, and simple work-up procedure, and it has the ability to tolerate a wide variety of substitutions in all three components, which is lacking in existing procedures.
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The indium(III) chloride-catalyzed von Pechmann reaction: a simple and effective procedure for the synthesis of 4-substituted coumarins

TL;DR: Indium(III) chloride is used as an efficient catalyst in the von Pechmann condensation of phenols with β-ketoesters leading to the formation of coumarin derivatives in excellent yields with good purity as mentioned in this paper.
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Hypervalent iodine mediated intramolecular cyclization of thioformanilides: expeditious approach to 2-substituted benzothiazoles.

TL;DR: A new, mild, and efficient method has been developed for the synthesis of 2-substituted benzothiazoles via the intramolecular cyclization of thioformanilides by using hypervalent iodine reagents in CH2Cl2 at ambient temperature.
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Effect of linker length on DNA-binding affinity, cross-linking efficiency and cytotoxicity of C8-linked pyrrolobenzodiazepine dimers

TL;DR: An efficient synthesis of a homologous series of C8-linked pyrrolobenzodiazepine dimers is reported; compounds with an odd number of methylenes in the linker show a higher affinity for DNA, enhanced cross-linking efficiency, and are more cytotoxic compared with compounds with either n= 4 or 6.
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An efficient, high yielding protocol for the synthesis of functionalized quinolines via the tandem addition/annulation reaction of o-aminoaryl ketones with α-methylene ketones

TL;DR: In this paper, a mild and efficient method was developed for the condensation of 2-aminoaryl ketones with α-methylene ketones in the presence of a catalytic amount of reusable catalyst CeCl 3 ·7H 2 O (25m) at ambient temperature to afford the corresponding poly-substituted quinolines in high yields under mild conditions.