Green Chemistry: Environmentally Benign Reactions, Second Edition
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Features
- Explains the need for and principles of green chemistry
- Covers a wide range of reactions, including solid state (solventless), photochemical, enzymatic, and sonication
- Discusses the planning and detailed preparations required to convert to green laboratory techniques
- Presents applications that are relevant to practicing researchers and environmental chemists working in industry, as well as to students
Summary
Covering a wide range of reactions, including solid state, photochemical, enzymatic, and sonication, this book explains the need for and the principles of green chemistry, including applications relevant to researchers and students. The author discusses the planning and detailed preparations that are required in order to convert to green laboratory techniques. The first part of this new second edition describes 58 reactions under normal and benign reactions. The second part provides experimental details for a number of green preparations. The first edition of the text won the American Library Association’s award for Outstanding Academic Title in their Choice magazine.
Table of Contents
Green Chemistry
The Need of Green Chemistry
Principles of Green Chemistry
Planning a Green Synthesis in a Chemical Laboratory
Green Reactions
Acyloin Condensation
Aldol Condensation
Arndt-Eistert Synthesis
Baeyer-Villiger Oxidation
Baker-Venkataraman Rearrangement
Barbier Reaction
Barton Reaction
Baylis-Hillman Reaction
Beckmann Rearrangement
Benzil-Benzilic Rearrangement
Benzoin Condensation
Biginelli Reaction
Bouveault Reaction
Cannizzaro Reaction
Claisen Rearrangement
Claisen-Schmidt Reaction
Clemmensen Reduction
Curtius Rearrangement
Dakin Reaction
Darzen Reaction
Dieckmann Condensation
Diels-Alder Reaction
Fischer-Indole Synthesis
Friedel Crafts Reaction
Friedlander Synthesis
Fries Rearrangement
Graebe-Ullman Synthesis
Grignard Reaction
Heck Reaction
Hantzsch Pyridine Synthesis
Henry Reaction
Hiyama Reaction
Hoffmann Elimination
Knoevenagel Condensation
Kolbe-Schmitt Reaction
Mannich Reaction
Meyer-Schuster Rearrangement
Michael Addition
Mukaiyama Reaction
Pechmann Condensation
Paterno-Büchi Reaction
Pauson-Khand Reaction
Pinacol Coupling
Pinacol-Pinacolone Rearrangement
Prins Reaction
Reformatsky Reaction
Rupe Rearrangement
Simmons-Smith Reaction
Sonogashira Reaction
Stetter Reaction
Stille Coupling Reaction
Strecker Synthesis
Suzuki Coupling Reaction
Ullmann Reaction
Weiss-Cook Reaction
Williamsons Ether Synthesis
Wittig Reaction
Wurtz Reaction
Author Bio(s)
V.K. Ahluwalia is a visiting professor at the Dr. B.R. Ambedkar Centre for Biomedical Research, University of Delhi, India.
