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Produktbild: Handbook of Green Chemistry - Green Solvents
Band 5

Handbook of Green Chemistry - Green Solvents

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Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Abbildungen

2 Farbabb.

Herausgeber

Chao-Jun Li

Verlag

Wiley-VCH

Seitenzahl

427

Maße (L/B/H)

2.7/17/24 cm

Gewicht

962 g

Auflage

1. Auflage

Sprache

Englisch

ISBN

978-3-527-32591-7

Beschreibung

Portrait

Series Editor:
Paul T. Anastas joined Yale University as Professor and iserves as the Director of the Center for Green Chemistry and Green Engineering at Yale. From 2004-2006, Paul Anastas has been the Director of the Green Chemistry Institute in Washington, D.C. Until June of 2004 he served as Assistant Director for Environment at e White House Office of Science and Technology Policy where his responsibilities included a wide range of environmental science issues including furthering international public-private cooperation in areas of Science for Sustainability such as Green Chemistry. In 1991, he established the industry-government-university partnership Green Chemistry Program, which was expanded to include basic research, and the Presidential Green Chemistry Challenge Awards. He has published and edited several books in the field of Green Chemistry and developed the 12 principles of Green Chemistry.
 
Volume Editor:
Professor Chao-Jun Li received his Ph.D at McGill University (Montreal, Canada) and did a NSERC Postdoctoral Fellow at Stanford University (USA). He was on the faculty at Tulane University (New Orleans, USA) until 2003. Since 2003, he has been at McGill University where he currently holds a Canada Research Chair (in Green Chemistry) and an E. B. Eddy Chair Professorship. He has published over 300 scientific publications and received numerous awards including the US Presidential Green Chemistry Challenge Award and the Canadian Green Chemistry and Engineering Award. He is a Fellow of the Royal Society of Canada (Academy of Science) and is an Associate Editor for "Green Chemistry" of the Royal Society of Chemistry (UK).

Produktdetails

Einband

Gebundene Ausgabe

Abbildungen

2 Farbabb.

Herausgeber

Chao-Jun Li

Verlag

Wiley-VCH

Seitenzahl

427

Maße (L/B/H)

2.7/17/24 cm

Gewicht

962 g

Auflage

1. Auflage

Sprache

Englisch

ISBN

978-3-527-32591-7

Herstelleradresse

Wiley-VCH GmbH
product_safety@wiley.com
Wiley-VCH GmbH, Boschstrasse 12, DE-69469 Weinheim

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  • Produktbild: Handbook of Green Chemistry - Green Solvents
  • THE PRINCIPLES OF AND REASONS FOR USING WATER AS A SOLVENT FOR GREEN CHEMISTRY
    Introduction
    Binding Two Species Together Driven by the Hydrophobic Effect in Water
    Aromatic Chlorination
    Acylation of Cyclodextrins by a Bound Ester
    Mimics of Metalloenzymes Using the Hydrophobic Effect in Water
    Mimics of the Enzyme Ribonuclease
    Mimics of Enzymes that Use Pyridoxamine Phosphate and Pyridoxal Phosphate as Coenzymes
    Artificial Enzymes Carrying Mimics of Thiamine Pyrophosphate
    Enolizations and Aldol Condensations
    Hydrophobic Acceleration of Diels-Alder Reactions
    Selectivities in Water Induced by the Hydrophobic Effect - Carbonyl Reductions
    Selectivities in Water Induced by the Hydrophobic Effect - Oxidations
    Using Hydrophobic Effects in Water to Determine the Geometries of Transition States for Some Important Reactions
    Conclusion
    GREEN ACID CATALYSIS IN WATER
    Introduction
    Lewis Acids in Water
    Chiral Lewis Acid-Catalyzed Asymmetric Reactions in Water
    Bronsted Acid Catalysis in Pure Water
    Conclusion and Perspective
    GREEN BASES IN WATER
    Introduction
    Types of Bases and Their Use from a Green Point of View
    Liquid-Liquid Processes
    Solid-Liquid Processes
    GREEN OXIDATION IN WATER
    Introduction
    Water-Soluble Ligands
    Oxidations Catalyzed by Metalloporphyrins and Metallophthalocyanines
    Epoxidation and Dihydroxylation of Olefins in Aqueous Media
    Alcohol Oxidations in Aqueous Media
    Aldehyde and Ketone Oxidations in Water
    Sulfoxidations in Water
    Conclusion
    GREEN REDUCTION IN WATER
    Introduction
    Water-Soluble Ligands
    Hydrogenation in Water
    Transfer Hydrogenation in Water
    Role of Water
    Conclusion
    COUPLING REACTIONS IN WATER
    Introduction
    Reaction of Carbonyl Compounds and Derivatives
    Reaction of Alkenes and Alkynes
    Reaction of Organic Halides and Derivatives
    Conclusion
    "ON WATER" FOR GREEN CHEMISTRY
    Introduction
    Pericyclic Reactions
    Addition of Heteronucleophiles to Unsaturated Carbonyl Compounds
    Enantioselective Direct Aldol Reactions
    Coupling Reactions
    Oxidation
    Bromination Reactions
    Miscellaneous Reactions
    Theoretical Studies
    Conclusion
    PERICYCLIC REACTIONS IN WATER. TOWARD GREEN CHEMISTRY
    Introduction
    Pericyclic Reaction in Aqueous Media
    Conclusion
    NON-CONVENTIONAL ENERGY SOURCES FOR GREEN SYNTHESIS IN WATER (MICROWAVE, ULTRASOUND, AND PHOTO)
    Introduction
    MW-Assisted Organic Transformations in Aqueous Media
    Sonochemical Organic Transformations in Aqueous Media
    Photochemical Transformations in Aqueous Media
    Conclusion
    FUNCTIONALIZATION OF CARBOHYDRATES IN WATER
    Introduction
    C-C Bond Formation Reactions
    C-N Bond Formation Reactions
    Functionalization of Hydroxy Groups
    Clyco-Organic Substrates and Reactions in Aqueous Sugar Solutions
    Conclusion
    WATER UNDER EXTREME CONDITIONS FOR GREEN CHEMISTRY
    Introduction
    Background
    Recent Progress in HTW Synthesis
    WATER AS A GREEN SOLVENT FOR PHARMACEUTICAL APPLICATIONS
    Introduction - Is Water a Green Solvent?
    Water-Based Enzymatic Processes
    Processes in Which the Product is Isolated by pH Adjustment to the Isoelectric Point
    Carbon-Carbon Bond-Forming Cross-Coupling Reactions in Water
    Pharmaceutical Processes Using Mixed Aqueous Solvents
    Conclusion
    WATER AS A GREEN SOLVENT FOR BULK CHEMICALS
    Introduction
    Hydroformylation - An Overview
    Water as Solvent for Hydroformylation
    Water as Solvent in the Production of 2,7-Octadien-1-ol (Kurayray Process)
    Conclusion