Suresh Kumar Mondal

ORCID: 0000-0002-8065-448X
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About
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Research Areas
  • Catalytic Cross-Coupling Reactions
  • Synthesis and Biological Evaluation
  • Synthesis and Characterization of Pyrroles
  • Crystallization and Solubility Studies
  • Catalytic C–H Functionalization Methods
  • X-ray Diffraction in Crystallography
  • Synthesis and biological activity
  • Cyclopropane Reaction Mechanisms
  • Chemical synthesis and alkaloids
  • Microbial Natural Products and Biosynthesis
  • Crystallography and molecular interactions
  • Synthesis and Reactivity of Heterocycles
  • Biochemical effects in animals
  • Catalytic Alkyne Reactions
  • Bacteriophages and microbial interactions
  • Multicomponent Synthesis of Heterocycles
  • Synthetic Organic Chemistry Methods
  • N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
  • SARS-CoV-2 and COVID-19 Research
  • Plant Virus Research Studies
  • Cancer therapeutics and mechanisms
  • Biochemical and Structural Characterization
  • Nanoparticles: synthesis and applications
  • Amino Acid Enzymes and Metabolism
  • Marine Sponges and Natural Products

Indian Institute of Technology Kharagpur
2020-2025

Haldia Institute of Technology
2013-2017

Vidyasagar University
2017

Antimicrobial resistance poses a serious threat to global health, necessitating the exploration of innovative solutions.

10.1039/d4pm00032c article EN cc-by-nc RSC Pharmaceutics 2024-01-01

To understand SARS-CoV-2 microevolution, this study explored the genome-wide frequency, gene-wise distribution, and molecular nature of all point-mutations detected across its 71,703 RNA-genomes deposited in GISAID till 21 August 2020. Globally, nsp1/nsp2 orf7a/orf3a were most mutation-ridden non-structural structural genes respectively. Phylogeny 4618 spatiotemporally-representative genomes revealed that entities belonging to early lineages are mostly spread over Asian countries, including...

10.1016/j.ygeno.2020.11.003 article EN cc-by-nc-nd Genomics 2020-11-01

N -Glycidyl d -tryptophan ether derivative may be suitable for use as ointment base to reduce the inflammation, ROS, DNA damage and bacterial load over wounds.

10.1039/d4md00878b article EN RSC Medicinal Chemistry 2025-01-01

An efficient one pot synthesis of polycyclic benzimidazole derivatives has been developed (up to 90% yield).

10.1039/c3ra44521f article EN RSC Advances 2013-11-14

We have reported a one-pot two step methodology for the synthesis of highly condensed pyrrolo[1,2-<italic>a</italic>][1,4]benzodiazepines by modified Pictet–Spengler reaction.

10.1039/c9ob00448c article EN Organic & Biomolecular Chemistry 2019-01-01

Herein, we report an efficient synthesis of N-substituted pyrrole derivatives and their application to construct macrocyclic oxazocinone via a two-component coupling reaction followed by base mediated intramolecular cyclization. This methodology provides easy two-step approach constitute library fused pyrrolo-oxazocinone in good yields under mild conditions. The present offers access the fluorescent pyrole derivatives. Among them, tert-butyl...

10.1039/c7ob00160f article EN Organic & Biomolecular Chemistry 2017-01-01

A novel class of bridgehead nitrogen heterocycles, pyrido[1,2-<italic>a</italic>]pyrimidinium ions, has been readily synthesized by a two-step one-pot reaction in high yields (up to 93%).

10.1039/c5ob01082a article EN Organic & Biomolecular Chemistry 2015-01-01

Herein, we report a rare pentacyclic N-fused hetrocycle synthesis via palladium catalyzed intramolecular C−H arylation along with the brief synthetic study of new type bicyclic/tricyclic pyrrole rings. This rings provided diversely substituted polycyclic nitrogen fused heterocycles from N-benzyl/N-benzyloxy pyrroles good to excellent yields.

10.1002/slct.201701800 article EN ChemistrySelect 2017-10-11

A short, efficient and general methodology for benzo[ b ]carbazolenaphthoquinones was developed via Pd‐catalyzed C‐H arylation process. This successfully applied to the synthesis of highly biologically active compound 5H–benzo[ ]carbazole‐6,11‐diones. Additionally, one‐pot ]phenazine‐6,11(5H,12H)‐dione derivatives also explored in aqueous medium.

10.1002/jhet.2832 article EN Journal of Heterocyclic Chemistry 2017-03-03

A simple and facile approach for the synthesis of various structurally different tricyclic bent oxepine frameworks from a readily accessible precursor has been introduced. The substituted derivative involved Pd(0)-catalyzed Heck reaction. This methodology enriches literature large ring formation.

10.1080/00397911.2016.1142566 article EN Synthetic Communications 2016-02-20

A novel synthesis of 3,4-fused furans (both tricyclic and bicyclic) through platinum-catalyzed cyclization 3-(2-formylcycloalkenyl)-acrylic amides 2 in methanol is described (up to 90% yield). Tricyclic dihydrofuran derivatives were also obtained via reductive 2. The substrates from β- bromovinyl aldehydes by a Pd-catalyzed Heck reaction.

10.1080/00397911.2014.974615 article EN Synthetic Communications 2014-11-03

Abstract A variety of pyrrole and isoquinoline derivatives (II), (IV), (VI) are synthesized via aza‐exo‐trig aza‐endo‐dig cyclization alkenyl or alkynyl carbaldehydes (I), (III), (V), respectively.

10.1002/chin.201649129 article EN ChemInform 2016-11-01

Abstract Fluorescence properties of the formed benzimidazoles in different solvents and at pH are investigated.

10.1002/chin.201436172 article EN ChemInform 2014-08-21
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