Organic chemistry, Catalysis, Stereochemistry, Palladium and Combinatorial chemistry are his primary areas of study. His Nitration, Stereoselectivity, Reagent and Olefin fiber study, which is part of a larger body of work in Organic chemistry, is frequently linked to Functional group, bridging the gap between disciplines. His Catalysis research is multidisciplinary, relying on both Aryl, Ligand, Surface modification and Phenols.
His study looks at the relationship between Surface modification and topics such as Biphenyl, which overlap with Meta-, Toluene and Phenol. His work carried out in the field of Stereochemistry brings together such families of science as Hydroxylation, Reactivity, Substrate, Copper and Bond formation. His Combinatorial chemistry study combines topics in areas such as Intermolecular force, Decarbonylation and Reaction mechanism.
The scientist’s investigation covers issues in Catalysis, Combinatorial chemistry, Organic chemistry, Palladium and Surface modification. His Catalysis research is multidisciplinary, incorporating elements of Aryl and Medicinal chemistry. The study incorporates disciplines such as Yield, Regioselectivity, Reactivity, Molecule and Selectivity in addition to Combinatorial chemistry.
His Selectivity research incorporates elements of Substrate and Cyanation. He interconnects Decarbonylation, Decarboxylation and Catalytic cycle in the investigation of issues within Palladium. His Surface modification study integrates concerns from other disciplines, such as Cascade, Stereochemistry, Polymer chemistry and Meta-.
His primary scientific interests are in Combinatorial chemistry, Catalysis, Surface modification, Transition metal and Regioselectivity. The concepts of his Combinatorial chemistry study are interwoven with issues in Aryl, Organic molecules, Cyanation and Palladium. To a larger extent, he studies Organic chemistry with the aim of understanding Catalysis.
His study on Chiral induction, Nitration and Phenols is often connected to Research studies and Deep eutectic solvent as part of broader study in Organic chemistry. He combines subjects such as Meta-, Group, Reactivity, Cascade and Selectivity with his study of Surface modification. His work carried out in the field of Transition metal brings together such families of science as Nanotechnology, Polymer chemistry and Enantioselective synthesis, Desymmetrization.
His scientific interests lie mostly in Combinatorial chemistry, Catalysis, Surface modification, Transition metal and Regioselectivity. His Combinatorial chemistry research incorporates themes from Palladium catalyst, Selectivity and Olefin fiber. His Selectivity research includes elements of Solvent, Palladium, Ether, Pyrimidine and Alkyne.
His studies deal with areas such as Heme, Enzyme and Nanotechnology as well as Catalysis. His research in Surface modification intersects with topics in Pharmacophore, Adduct, Sonogashira coupling and Meta-. The study incorporates disciplines such as Group, Lewis acids and bases, Polymer chemistry and Organic molecules in addition to Regioselectivity.
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Palladium-Catalyzed Coupling of Functionalized Primary and Secondary Amines with Aryl and Heteroaryl Halides: Two Ligands Suffice in Most Cases
Debabrata Maiti;Brett P. Fors;Jaclyn L. Henderson;Yoshinori Nakamura.
Chemical Science (2011)
Reactions of a copper(II) superoxo complex lead to C-H and O-H substrate oxygenation: modeling copper-monooxygenase C-H hydroxylation.
Debabrata Maiti;Dong-Heon Lee;Dong-Heon Lee;Katya Gaoutchenova;Christian Würtele.
Angewandte Chemie (2008)
Oxidative Trifluoromethylation of Unactivated Olefins: An Efficient and Practical Synthesis of α‐Trifluoromethyl‐Substituted Ketones
Arghya Deb;Srimanta Manna;Atanu Modak;Tuhin Patra.
Angewandte Chemie (2013)
Remote para-C-H Functionalization of Arenes by a D-Shaped Biphenyl Template-Based Assembly.
Sukdev Bag;Tuhin Patra;Atanu Modak;Arghya Deb.
Journal of the American Chemical Society (2015)
Orthogonal Cu- and Pd-Based Catalyst Systems for the O-and N-Arylation of Aminophenols
Debabrata Maiti;Stephen L. Buchwald.
Journal of the American Chemical Society (2009)
Cu-Catalyzed Arylation of Phenols: Synthesis of Sterically Hindered and Heteroaryl Diaryl Ethers
Debabrata Maiti;Stephen L. Buchwald.
Journal of Organic Chemistry (2010)
A 1:1 copper-dioxygen adduct is an end-on bound superoxo copper(II) complex which undergoes oxygenation reactions with phenols.
Debabrata Maiti;H. Christopher Fry;Julia S. Woertink;Michael A. Vance.
Journal of the American Chemical Society (2007)
Palladium-catalyzed aryl C-H olefination with unactivated, aliphatic alkenes.
Arghya Deb;Sukdev Bag;Rajesh Kancherla;Debabrata Maiti.
Journal of the American Chemical Society (2014)
Decarboxylation as the Key Step in C−C Bond‐Forming Reactions
Tuhin Patra;Debabrata Maiti.
Chemistry: A European Journal (2017)
Palladium-Catalyzed Synthesis of Benzofurans and Coumarins from Phenols and Olefins†
Upendra Sharma;Togati Naveen;Arun Maji;Srimanta Manna.
Angewandte Chemie (2013)
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