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Green Synthetic Approaches for Biologically Relevant Heterocycles

Volume 2: Green Catalytic Systems and Solvents

Green Synthetic Approaches for Biologically Relevant Heterocycles, Second Edition, Volume Two: Green Catalytic Systems and Solvents reviews this significant group of organic c… Read more

Description

Green Synthetic Approaches for Biologically Relevant Heterocycles, Second Edition, Volume Two: Green Catalytic Systems and Solvents reviews this significant group of organic compounds within the context of sustainable methods and processes, expanding on the first edition with fully updated coverage and a whole range of new chapters. Volume Two explores green catalytic systems and solvents and the techniques surrounding this approach, including metal and magnetic catalysis to organocatalysis and solid acid catalysis, cycloaddition reactions, and varied approaches using ionic liquids.

This updated edition is an essential resource on sustainable approaches for academic researchers, R&D professionals, and students working across medicinal, organic, natural product and green chemistry.

Key features

  • Provides fully updated coverage of the field with an emphasis on sustainability
  • Highlights a range of different eco-friendly solvents and environmentally-friendly catalysts
  • Collates the experience of a global team of expert contributors

Readership

Organic, Natural Product, Synthetic and Green Chemists across both academia and industry Chemical Engineers, Sustainability Scientists

Table of contents

1. Green synthetic approaches for biologically relevant heterocycles: Green catalytic systems and solvents - an overview

2. Synthesis of bioactive five- and six-membered heterocycles catalyzed by heterogeneous supported metals

3. Metal-catalyzed routes for the synthesis of furocoumarins and coumestans

4. Green solvents for eco-friendly synthesis of bioactive heterocyclic compounds

5. Use of environmentally friendly magnetic catalysts for heterocycles

6. Proline and proline-derived organocatalysts in the synthesis of heterocycles

7. Synthesis of heterocyclic building blocks and natural products by solid acid catalysis

8. Ionic liquids prompted synthesis of biologically relevant five and six-membered heterocyclic skeletons: An update

9. Heterocycles-based ionic liquid-supported synthesis of small organic molecules

10. Green and catalytic methods for ?-lactone synthesis

11. Cycloaddition reactions in ionic liquids for the synthesis of biologically relevant heterocycles

12. Green synthetic approaches for medium ring-sized heterocycles of biological interest

13. Sustainable synthesis of benzimidazoles, quinoxalines and congeners

Product details

About the editor

GB

Goutam Brahmachari

Dr. Goutam Brahmachari is a full professor of organic chemistry at Visva-Bharati University, Santiniketan, India. His research focuses on developing practical synthetic methods for carbon–carbon and carbon–heteroatom bonds using C–H functionalization, cascade, and cross-coupling techniques, with applications in medicinal heterocyclic scaffolds. He has also studied the chemistry and biology of traditionally used Indian medicinal plants, identifying novel phytochemicals of interest.

He is the founding Series Editor of Elsevier’s Natural Product Drug Discovery book series and an elected fellow of the Royal Society of Chemistry. His awards include the Acharya P. C. Ray Memorial Lecture Award (2025) from the Indian Science News Association (ISNA), Kolkata, India; the Dr. Satyajit Chakraborti Memorial Award (2025) from IEM, Kolkata, India; the Chemical Research Society of India Bronze Medal (2021); the Dr. Basudev Banerjee Memorial Award (2021) from the Indian Chemical Society; the Indian National Science Academy Teachers Award (2019); the Dr. Kalam Best Teaching Faculty Award (2017); and the Academic Brilliance Award (2015).
Affiliations and expertise
Full Professor, Laboratory of Natural Products & Organic Synthesis, Department of Chemistry, Siksha-Bhavana, Visva-Bharati (a Central University), Santiniketan, West Bengal, India

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