S
Suman Sinha
Researcher at Indian Institute of Engineering Science and Technology, Shibpur
Publications - 16
Citations - 695
Suman Sinha is an academic researcher from Indian Institute of Engineering Science and Technology, Shibpur. The author has contributed to research in topics: Ligand & Diradical. The author has an hindex of 11, co-authored 15 publications receiving 456 citations.
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Journal ArticleDOI
One-Pot Cascade Synthesis of Quinazolin-4(3H)-ones via Nickel-Catalyzed Dehydrogenative Coupling of o-Aminobenzamides with Alcohols
TL;DR: A general, efficient, and environmentally benign method for the one-pot cascade synthesis of quinazolin-4(3H)-ones via acceptorless dehydrogenative coupling of o-aminobenzamide with alcohols catalyzed by a simple Ni(II) catalyst, featuring a tetraaza macrocyclic ligand (tetramethyltetraaza[14]annulene (MeTAA).
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Dehydrogenative Synthesis of Quinolines, 2-Aminoquinolines, and Quinazolines Using Singlet Diradical Ni(II)-Catalysts
Gargi Chakraborty,Rina Sikari,Siuli Das,Rakesh Mondal,Suman Sinha,Seemika Banerjee,Nanda D. Paul +6 more
TL;DR: Insight was carried out into the reaction mechanism which shows that the nickel and the coordinated diamine ligands participate in a synergistic way during the dehydrogenation of alcohols.
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Accessing Polysubstituted Quinazolines via Nickel Catalyzed Acceptorless Dehydrogenative Coupling
TL;DR: Two environmentally benign methods for the synthesis of quinazolines via acceptorless dehydrogenative coupling of 2-aminobenzylamine with benzyl alcohol and benzonitrile and tetraaza macrocyclic ligands are reported.
Journal ArticleDOI
Metal-Ligand Cooperative Approach To Achieve Dehydrogenative Functionalization of Alcohols to Quinolines and Quinazolin-4(3 H )-ones under Mild Aerobic Conditions.
Siuli Das,Suman Sinha,Deepannita Samanta,Rakesh Mondal,Gargi Chakraborty,Paula Brandão,Nanda D. Paul +6 more
TL;DR: Control experiments and deuterium labelling studies indicate that both copper and the coordinated azo-aromatic ligand participate in a cooperative manner during the catalytic cycle.
Journal ArticleDOI
A nickel catalyzed acceptorless dehydrogenative approach to quinolines
TL;DR: A general, efficient and environmentally benign, one-step synthesis of substituted quinoline derivatives was achieved by acceptorless dehydrogenative coupling of o-aminobenzylalcohols with ketones and secondary alcohols catalyzed by a cheap, earth abundant and easy to prepare nickel catalyst.