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Full Description
Many new methods directed to organic and inorganic syntheses of useful intermediates are being developed to specifically address green and sustainable chemistry principles. Highlighting the importance of green metrics, the Green Syntheses series focuses on how to reliably substantiate and validate the level of "greenness" of chemical processes, providing practical synthetic methodologies and metrics for a rigorous proof of "greenness." In Green Syntheses, Volume 1, the first book of its kind, the editors determine appropriate material efficiency green metrics and use them to compare syntheses provided by the chapter authors with those previously published.
Presenting a new concept in green chemistry, this book demonstrates what future publications might look like if green principles are followed and also incorporate the important ethical aspect of supplying rigorous procedures in laboratory practice and evidence of greenness of a given synthesis protocol using metrics analysis. This inaugural volume initiates the much-needed transition from stating the 12 guiding principles on the philosophy of green chemistry to the actualization and verification of it.
The book addresses primarily the issue of material efficiency metrics, which measure the amount of waste produced relative to desired product. In each contributed example, full experimental details are given showing all quantities of materials used in the procedure. Authors discuss the green merits of their protocols in conjunction with the results of a thorough metrics analysis, allowing for in-depth discussion of insights about synthesis strategy and performance characteristics of the new and prior cited plans.
Contents
Introduction to the Green Syntheses Series. Application of Material Efficiency Metrics to Assess Reaction Greenness—Illustrative Case Studies from Organic Syntheses. Reaction 1: Synthesis of 3-Benzyl-5-Methyleneoxazolidin-2-one from N-Benzylprop-2-yn-1-Amine and CO2. Reaction 2: Synthesis of the 5-Membered Cyclic Carbonates from Epoxides and CO2. Part I: Green Methods for the Epoxidation of Olefins Using Venturello Anion-Based Catalysts. Part II: Green Methods for the Epoxidation of Olefins Using Lacunary-Type Phosphotungstate Anion-Based catalysts. Solvent-Free Flavone Synthesis reaction Using KHSO4 as Recyclable Catalyst. Waste Minimized Synthesis of γ-Nitroketones. Green Syntheses of Ethers and Esters Using Dimethyl Carbonate. Synthesis of Ethyl Octyl Ether by Reaction between 1-Octanol and Ethanol over Amberlyst 70. Reaction: Organocatalytic Asymmetric Tandem Epoxidation-Passerini Reaction . Reaction: Green Synthesis of Chalcone and Coumarin Derivatives via a Suzuki Cross-Coupling Reaction. Enzymatic-Synthesized Hydroxy-L-Prolines as Asymmetric Catalysts for Green Synthesis. Green Synthesis of Homoallylic Silyl Ethers. Environmentally-Friendly Synthesis of Norstatines in Water. Five-Membered and N- and O-Heterocycles by Dimethyl Carbonate Chemistry. Acronym Index . Compound Index. Formula Index. Subject Index.
