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Debabrata Maiti
Researcher at Indian Institute of Technology Bombay
Publications - 299
Citations - 12334
Debabrata Maiti is an academic researcher from Indian Institute of Technology Bombay. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 55, co-authored 242 publications receiving 9017 citations. Previous affiliations of Debabrata Maiti include Tokyo Institute of Technology & Johns Hopkins University.
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Palladium-Catalyzed Coupling of Functionalized Primary and Secondary Amines with Aryl and Heteroaryl Halides: Two Ligands Suffice in Most Cases
TL;DR: Two catalyst systems, based on the ligands BrettPhos and RuPhos, are reported, which provide the widest scope for Pd-catalyzed C-N cross-coupling reactions to date.
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Remote para-C-H Functionalization of Arenes by a D-Shaped Biphenyl Template-Based Assembly.
Sukdev Bag,Tuhin Patra,Atanu Modak,Arghya Deb,Soham Maity,Uttam Dutta,Aniruddha Dey,Rajesh Kancherla,Arun Maji,Avijit Hazra,Milan Bera,Debabrata Maiti +11 more
TL;DR: An easily recyclable, novel Si-containing biphenyl-based template is reported that directs efficient functionalization of the distal p-C-H bond of toluene by forming a D-shaped assembly that allows the required flexibility to support the formation of an oversized pre-transition state.
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Decarboxylation as the Key Step in C−C Bond‐Forming Reactions
Tuhin Patra,Debabrata Maiti +1 more
TL;DR: This Review provides an overview on the most recent progress in the field of C-C bond formation involving decarboxylation as a key step involving carboxylic acid.
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Accessing Remote meta- and para-C(sp 2 )-H Bonds with Covalently Attached Directing Groups.
TL;DR: This Review compiles the significant achievements made in this field of both meta- and para-selectivity using covalently attached directing groups, which are systematically classified on the basis of their mode of covalent attachment to the substrate as well as their chemical nature.
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Oxidative Trifluoromethylation of Unactivated Olefins: An Efficient and Practical Synthesis of α‐Trifluoromethyl‐Substituted Ketones
TL;DR: The incorporation of a CF3 group in a compound of pharmacological relevance usually results in significant enhancement of its lipophilicity, binding selectivity, and metabolic stability.