S
Sujit Roy
Researcher at Indian Institute of Technology Bhubaneswar
Publications - 209
Citations - 3937
Sujit Roy is an academic researcher from Indian Institute of Technology Bhubaneswar. The author has contributed to research in topics: Catalysis & Alkylation. The author has an hindex of 37, co-authored 204 publications receiving 3682 citations. Previous affiliations of Sujit Roy include Bhabha Atomic Research Centre & Indian Institute of Technology Kanpur.
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In vivo response of porous hydroxyapatite and beta-tricalcium phosphate prepared by aqueous solution combustion method and comparison with bioglass scaffolds.
Samir Ghosh,Samit Kumar Nandi,Biswanath Kundu,Someswar Datta,Dipak Kumar De,Sujit Roy,Debabrata Basu +6 more
TL;DR: Lower bone ingrowth and reduced strength was observed with HAp compared to beta-TCP/bioglass-based implants, which varied according to the composition of the implanting material, which could be tailored through this novel synthesis.
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Cooperative friedel-crafts catalysis in heterobimetallic regime : Alkylation of aromatics by π-activated alcohols
TL;DR: From dual-catalyst combination studies varying the transition metal and main group metal partner, the efficiency of the present catalysts is attributed to the electrophilic "IrIII-SnIV" core.
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A study of self-propagating high-temperature synthesis of NiAl in thermal explosion mode
TL;DR: In this article, the effect of the rate of heating both on the pre-combustion reaction and the combustion in the case of thermal explosion was investigated in self-propagating high-temperature synthesis.
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Catalytic Hunsdiecker Reaction of α,β-Unsaturated Carboxylic Acids: How Efficient Is the Catalyst?
Jaya Prakash Das,Sujit Roy +1 more
TL;DR: In this article, the relative efficiency of triethylamine, tetrabutylammonium trifluoroacetate, and lithium acetate as catalysts for the conversion of 4-methoxycinnamic acid to 4mETHoxy-β-bromostyrene was evaluated.
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Dual-reagent catalysis within Ir-Sn domain: highly selective alkylation of arenes and heteroarenes with aromatic aldehydes.
TL;DR: This 100% TRAM selective transformation is clean and eliminates the use of acid systems.