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1.

電子ブック
ＥＢ
1. Applied homogeneous catalysis with organometallic compounds : : a comprehensive handbook in four volumes
edited by Boy Cornils, Wolfgang A. Herrmann, Matthias Beller, and Rocco Paciello
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電子ブック
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2. Lewis base catalysis in organic synthesis.. 1st
Edwin Vedejs and Scott E. Denmark
出版情報:   1 online resource (1441 pages)
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3. Catalysis without precious metals /
edited by R. Morris Bullock
出版情報: Weinheim : Wiley-VCH, 〓2010  1 online resource (xviii, 290 pages)
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Preface
List of Contributors
Catalysis Involving the H* Transfer Reactions of First-Row Transition Metals / John Hartung ; Jack R. Norton1：
H* Transfer Between M-H Bonds and Organic Radicals / 1.1：
H* Transfer Between Ligands and Organic Radicals / 1.2：
H* Transfer Between M-H and C-C Bonds / 1.3：
Chain Transfer Catalysis / 1.4：
Catalysis of Radical Cydizations / 1.5：
Competing Methods for the Cyclization of Dienes / 1.6：
Summary and Conclusions / 1.7：
References
Catalytic Reduction of Dinitrogen to Ammonia by Molybdenum / Richard R. Schrock2：
Some Characteristics of Triamidoamine Complexes / 2.1Introduction：
Possible [HIPTN3N]Mo Intermediates in a Catalytic Reduction of Molecular Nitrogen / 2.3：
MoN2 and MoN2- / 2.3.1：
Mo-N=NH / 2.3.2：
Conversion of Mo(N2) into Mo-N=NH / 2.3.3：
[Mo=N-NH2]+ / 2.3.4：
Mo=N and [Mo=NH]+ / 2.3.5：
Mo(NH3) and [Mo(NH3)+ / 2.3.6：
Interconversion of Mo(NH3) and Mo(N2) / 2.4：
Catalytic Reduction of Dinitrogen / 2.5：
MoH and Mo(H2) / 2.6：
Ligand and Metal Variations / 2.7：
Comments / 2.8：
Acknowledgements
Molybdenum and Tungsten Catalysts for Hydrogenation, Hydrosilylation and Hydrolysis / R. Morris Bullock3：
Introduction / 3.1：
Proton Transfer Reactions of Metal Hydrides / 3.2：
Hydride Transfer Reactions of Metal Hydrides / 3.3：
Stoichiometric Hydride Transfer Reactivity of Anionic Metal Hydride Complexes / 3.4：
Catalytic Hydrogenation of Ketones with Anionic Metal Hydrides / 3.5：
Ionic Hydrogenation of Ketones Using Metal Hydrides and Added Acid / 3.6：
Ionic Hydrogenations from Dihydrides: Delivery of the Proton and Hydride from One Metal / 3.7：
Catalytic Ionic Hydrogenations With Mo and W Catalysts / 3.8：
Mo Phosphine Catalysts With Improved lifetimes / 3.9：
Tungsten Hydrogenation Catalysts with N-Heterocyclic Carbene Ligands / 3.10：
Catalysts for Hydrosilylation of Ketones / 3.11：
Cp2Mo Catalysts for Hydrolysis, Hydrogenations and Hydrations / 3.12：
Conclusion / 3.13：
Modern Alchemy: Replacing Precious Metals with Iron in Catalytic Alkene and Carbonyl Hydrogenation Reactions / Paul J. Chink4：
Alkene Hydrogenation / 4.1：
Iron Carbonyl Complexes / 4.2.1：
Iron Phosphine Compounds / 4.2.2：
Bis(imino)pyridine Iron Complexes / 4.2.3：
α-Diimine Iron Complexes / 4.2.4：
Carbonyl Hydrogenation / 4.3：
Hydrosilylation / 4.3.1：
Bifunctional Complexes / 4.3.2：
Outlook / 4.4：
Olefin Oligomerizations and Polymerizations Catalyzed by Iron and Cobalt Complexes Bearing Bis(imino)pyridine Ligands / Vernon C. Gibson ; Gregory A. Solan5：
Precatalyst Synthesis / 5.1：
Ligand Preparation / 5.2.1：
Complexation with MX2 (M = Fe, Co) / 5.2.2：
Precatalyst Activation and Catalysis / 5.3：
Olefin Polymerization / 5.3.1：
Catalytic Evaluation / 5.3.1.1：
Steric Versus Electronic Effects / 5.3.1.2：
Effect of MAO Concentration / 5.3.1.3：
Effects of Pressure and Temperature / 5.3.1.4：
α-Olefin Monomers / 5.3.1.5：
Olefin Oligomerization / 5.3.2：
Substituent Effects / 5.3.2.1：
Schulz-Flory Distributions / 5.3.2.3：
Poisson Distributions / 5.3.2.4：
The Active Catalyst and Mechanism / 5.3.2.5：
Active Species / 5.4.：
Iron Catalyst / 5.4.1.1：
Cobalt Catalyst / 5.4.1.2：
Propagation and Chain Transfer Pathways/Theoretical Studies / 5.4.2：
Well-Defined Iron and Cobalt Alkyls / 5.4.3：
Other Applications / 5.5：
Immobilization / 5.5.1：
Reactor Blending and Tandem Catalysis / 5.5.2：
Conclusions and Outlook / 5.6：
Cobalt and Nickel Catalyzed Reactions Involving C-H and C-N Activation Reactions / Renee Becker ; William D. Jones6：
Catalysis with Cobal / 6.1：
Catalysis with Nickel / 6.3：
A Modular Approach to the Development of Molecular Electrocatalysts for H2 Oxidation and Production Based on Inexpensive Metals / M. Rakowski DuBois ; Daniel L. DuBois7：
Concepts in Catalyst Design Based on Structural Studies of Hydrogenase Enzymes / 7.1：
A Layered or Modular Approach to Catalyst Design / 7.3：
Using the First Coordination Sphere to Control the Energies of Catalytic Intermediates / 7.4：
Using the Second Coordination Sphere to Control the Movement of Protons between the Metal and the Exterior of the Molecular Catalyst / 7.5：
Integration of the First and Second Coordination Spheres / 7.6：
Summary / 7.7：
Nickel-Catalyzed Reductive Couplings and Cyclizations / Hasnain A. Malik ; Ryan D. Baxter ; John Montgomery8：
Couplings of Alkynes with α,β-Unsaturated Carbonyls / 8.1：
Three-Component Couplings via Alkyl Group Transfer-Methods Development / 8.2.1：
Reductive Couplings via Hydrogen Atom Transfer-Methods Development / 8.2.2：
Mechanistic Insights / 8.2.3：
Metallacycle-Based Mechanistic Pathway / 8.2.3.1：
Use in Natural Product Synthesis / 8.2.4：
Couplings of Alkynes with Aldehydes / 8.3：
Three-Component Couplings via Alkyl Group Transfer-Method Development / 8.3.1：
Reductive Couplings via Hydrogen Atom Transfer-Method Development / 8.3.2：
Simple Aldehyde and Alkyne Reductive Couplings / 8.3.2.1：
Directed Processes / 8.3.2.2：
Diastereoselective Variants: Transfer of Chirality / 8.3.2.3：
Asymmetric Variants / 8.3.2.4：
Cydocondensations via Hydrogen Gas Extrusion / 8.3.3：
Copper-Catalyzed Ligand Promoted Ullmann-type Coupling Reactions / Yongwen Jiang ; Dawei Ma8.3.5：
C-N Bond Formation / 9.1：
Arylation of Amines / 9.2.1：
Arylation of Aliphatic Primary and Secondary Amines / 9.2.1.1：
Arylation of Aryl Amines / 9.2.1.2：
Arylation of Ammonia / 9.2.1.3：
Arylation and Vinylation of N-Heterocycles / 9.2.2：
Coupling of Aryl Halides and N-Heterocycles / 9.2.2.1：
Coupling of Vinyl Bromides and N-Heterocycles / 9.2.2.2：
Aromatic Amidation / 9.2.3：
Cross-Coupling of aryl Halides with Amides and Carbamates / 9.2.3.1：
Cross-Coupling of Vinyl Halides with Amides or Carbamates / 9.2.3.2：
Cross-Coupling of Alkynl Halides with Amides or Carbamates / 9.2.3.3：
Azidation / 9.2.4：
C-0 Bond Formation / 19.3：
Synthesis of Diaryl Ethers / 9.3.1：
Aryloxylation of Vinyl Halides / 9.3.2：
Cross-Coupling of Aryl Halides with Aliphatic Alcohols / 9.3.3：
C-C Bond Formation / 9.4：
Cross-Coupling with Terminal Acetylene / 9.4.1：
The Arylation of Activated Methylene Compounds / 9.4.2：
Cyanation / 9.4.3：
C-S Bond Formation / 9.5：
The Formation of Bisaryl- and Arylalkyl-Thioethers / 9.5.1：
The Synthesis of Alkenylsulfides / 9.5.2：
Assembly of aryl Sulfones / 9.5.3：
C-P Bond Formation / 9.6：
Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC) / M.G. Finn ; Valery V. Fokin9.7：
Azide-Alkyne Cycloaddition: Basics / 10.1：
Copper-Catalyzed Cycloadditions / 10.3：
Catalysts and Ligands / 10.3.1：
CuAAC with In Situ Generated Azides / 10.3.2：
Mechanistic Aspects of the CuAAC / 10.3.3：
Reactions of Sulfonyl Azides / 10.3.4：
Copper-Catalyzed Reactions with Other Dipolar Species / 10.3.5：
Examples of Application of the CuAAC Reaction / 10.3.6：
Synthesis of Compound libraries for Biological Screening / 10.3.6.1：
Copper-Binding Adhesives / 10.3.6.2：
Representative Experimental Procedures / 10.3.7：
"Frustrated Lewis Pairs": A Metal-Free Strategy for Hydrogenation Catalysis / Douglas W. Stephan11：
Phosphine-Borane Activation of H2 / 11.1：
"Frustrated Lewis Pairs" / 11.2：
Metal-Free Catalytic Hydxogenation / 11.3：
Future Considerations / 11.4：
Index
Preface
List of Contributors
Catalysis Involving the H* Transfer Reactions of First-Row Transition Metals / John Hartung ; Jack R. Norton1：
4.

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4. Chemical catalysts for biomass upgrading / (: electronic bk)
edited by Mark Crocker, Eduardo Santillan-Jimenez
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Preface
Upgrading of Biomass via Catalytic Fast Pyrolysis (CFP) / Charles A. Mullen1：
Introduction / 1.1：
Catalytic Pyrolysis Over Zeolites / 1.1.1：
Catalytic Pyrolysis Over HZSM-5 / 1.1.1.1：
Deactivation of HZSM-5 During CFP / 1.1.1.2：
Modification of ZSM-5 with Metals / 1.1.1.3：
Modifications of ZSM-5 Pore Structure / 1.1.1.4：
CFP with Metal Oxide Catalysts / 1.1.2：
CFP to Produce Fine Chemicals / 1.1.3：
Outlook and Conclusions / 1.1.4：
References
The Upgrading of Bio-Oil via Hydrodeoxygenation / Adetoyese O. Oyedun and Madhumita Patel and Mayank Kumar and Amit Kumar2：
Hydrodeoxygenation (HDO) / 2.1：
Hydrodeoxygenation of Phenol as a Model Compound / 2.2.1：
HDO of Phenolic (Guaiacol) Model Compounds / 2.2.1.1：
HDO of Phenolic (Anisole) Model Compounds / 2.2.1.2：
HDO of Phenolic (Cresol) Model Compounds / 2.2.1.3：
Hydrodeoxygenation of Aldehyde Model Compounds / 2.2.2：
Hydrodeoxygenation of Carboxylic Acid Model Compounds / 2.2.3：
Hydrodeoxygenation of Alcohol Model Compounds / 2.2.4：
Hydrodeoxygenation of Carbohydrate Model Compounds / 2.2.5：
Chemical Catalysts for the HDO Reaction / 2.3：
Catalyst Promoters for HDO / 2.3.1：
Catalyst Supports for HDO / 2.3.2：
Catalyst Selectivity for HDO / 2.3.3：
Catalyst Deactivation During HDO / 2.3.4：
Research Gaps / 2.4：
Conclusions / 2.5：
Acknowledgments
Upgrading of Bio-oil via Fluid Catalytic Cracking / Idoia Hita and Jose Maria Arandes and Javier Bilbao3：
Bio-oil / 3.1：
Bio-oil Production via Fast Pyrolysis / 3.2.1：
General Characteristics, Composition, and Stabilization of Bio-oil / 3.2.2：
Adjustment of Bio-oil Composition Through Pyrolytic Strategies / 3.2.2.1：
Bio-oil Stabilization / 3.2.2.2：
Valorization Routes for Bio-oil / 3.2.3：
Hydroprocessing / 3.2.3.1：
Steam Reforming / 3.2.3.2：
Extraction of Valuable Components from Bio-oil / 3.2.3.3：
Catalytic Cracking of Bio-oil: Fundamental Aspects / 3.3：
The FCC Unit / 3.3.1：
Cracking Reactions and Mechanisms / 3.3.2：
Cracking of Oxygenated Compounds / 3.3.3：
Cracking of Bio-oil / 3.3.4：
Bio-oil Cracking in the FCC Unit / 3.4：
Cracking of Model Oxygenates / 3.4.1：
Coprocessing of Oxygenates and Their Mixtures with Vacuum Gas Oil (VGO) / 3.4.2：
Cracking of Bio-oil and Its Mixtures with VGO / 3.4.3：
Conclusions and Critical Discussion / 3.5：
Stabilization of Bio-oil via Esterification / Xun Hu4：
Reactions of the Main Components of Bio-Oil Under Esterification Conditions / 4.1：
Sugars / 4.2.1：
Carboxylic Acids / 4.2.2：
Furans / 4.2.3：
Aldehydes and Ketones / 4.2.4：
Phenolics / 4.2.5：
Other Components / 4.2.6：
Processes for Esterification of Bio-oil / 4.3：
Esterification of Bio-oil Under Subcritical or Supercritical Conditions / 4.3.1：
Removal of the Water in Bio-oil to Enhance Conversion of Carboxylic Acids / 4.3.2：
In-line Esterification of Bio-oil / 4.3.3：
Esterification Coupled with Oxidation / 4.3.4：
Esterification Coupled with Hydrogenation / 4.3.5：
Steric Hindrance in Bio-oil Esterification / 4.3.6：
Coking in Esterification of Bio-oil / 4.3.7：
Effects of Bio-oil Esterification on the Subsequent Hydrotreatment / 4.3.8：
Catalysts / 4.4：
Summary and Outlook / 4.5：
Catalytic Upgrading of Holocellulose-Derived C5 and C6 Sugars / Xingguang Zhang and Zhijun Tai and Amin Osatiashtiani and Lee Durndell and Adam F. Lee and Karen Wilson5：
Catalytic Transformation of C5-C6 Sugars / 5.1：
Isomerization Catalysts / 5.2.1：
Zeolites / 5.2.1.1：
Hydrotalcites / 5.2.1.2：
Other Solid Catalysts / 5.2.1.3：
Dehydration Catalysts / 5.2.2：
Zeolitic and Mesoporous Brønsted Solid Acids / 5.2.2.1：
Sulfonic Acid Functionalized Hybrid Organic-Inorganic Silicas / 5.2.2.2：
Metal-Organic Frameworks / 5.2.2.3：
Supported Ionic Liquids / 5.2.2.4：
Catalysts for Tandem Isomerization and Dehydration of C5-C6 Sugars / 5.2.3：
Bifunctional Zeolites and Mesoporous Solid Acids / 5.2.3.1：
Metal Oxides, Sulfates, and Phosphates / 5.2.3.2：
Catalysts for the Hydrogenation of C5-C6 Sugars / 5.2.3.3：
Ni Catalysts / 5.2.4.1：
Ru Catalysts / 5.2.4.2：
Pt Catalysts / 5.2.4.3：
Other Hydrogenation Catalysts / 5.2.4.4：
Hydrogenolysis Catalysts / 5.2.5：
Other Reactions / 5.2.6：
Conclusions and Future Perspectives / 5.3：
Chemistry of C-C Bond Formation Reactions Used in Biomass Upgrading: Reaction Mechanisms, Site Requirements, and Catalytic Materials / Tuong V. Bui and Nhung Duong and Felipe Anaya and Duong Ngo and Gap Warakunwit and Daniel E. Resasco6：
Mechanisms and Site Requirements of C-C Coupling Reactions / 6.1：
Aldol Condensation: Mechanism and Site Requirement / 6.2.1：
Base-Catalyzed Aldol Condensation / 6.2.1.1：
Acid-Catalyzed Aldol Condensation: Mechanism and Site Requirement / 6.2.1.2：
Alkylation: Mechanism and Site Requirement / 6.2.2：
Lewis Acid-Catalyzed Alkylation Mechanism / 6.2.2.1：
Brønsted Acid-Catalyzed Alkylation Mechanism / 6.2.2.2：
Base-Catalyzed Alkylation: Mechanism and Site Requirement / 6.2.2.3：
Hydroxyalkylation: Mechanism and Site Requirement / 6.2.3：
Brønsted Acid-Catalyzed Mechanism / 6.2.3.1：
Site Requirement / 6.2.3.2：
Acylation: Mechanism and Site Requirement / 6.2.4：
Mechanistic Aspects of Acylation Reactions / 6.2.4.1：
Role of Brønsted vs. Lewis Acid in Acylation Over Zeolites / 6.2.4.2：
Ketonization: Mechanism and Site Requirement / 6.2.5：
Mechanism of Surface Ketonization / 6.2.5.1：
Optimization and Design of Catalytic Materials for C-C Bond Forming Reactions / 6.2.5.2：
Oxides / 6.3.1：
Magnesia (MgO) / 6.3.1.1：
Zirconia (ZrO2) / 6.3.1.2：
ZSM-5 / 6.3.2：
HY / 6.3.2.2：
HBEA / 6.3.2.3：
Downstream Conversion of Biomass-Derived Oxygenates to Fine Chemicals / Michèle Besson and Stéphane Loridant and Noémie Perret and Catherine Pinel7：
Selective Catalytic Oxidation / 7.1：
Catalytic Oxidation of Glycerol / 7.2.1：
Glycerol to Glyceric Acid (GLYAC) / 7.2.2.1：
Glycerol to Tartronic Acid (TARAC) / 7.2.2.2：
Glycerol to Dihydroxyacetone (DHA) / 7.2.2.3：
Glycerol to Mesoxalic Acid (MESAC) / 7.2.2.4：
Glycerol to Glycolic Acid (GLYCAC) / 7.2.2.5：
Glycerol to Lactic Acid (LAC) / 7.2.2.6：
Oxidation of 5-HydroxymethylfurfuraI (HMF) / 7.2.3：
HMF to 2,5-Furandicarboxylic Acid (FDCA) / 7.2.3.1：
HMF to 2,5-Diformylfuran (DFF) / 7.2.3.2：
HMF to 5-Hydroxymethyl-2-furancarboxylic Acid (HMFCA) or 5-Formyl-2-furancarboxylic Acid (FFCA) / 7.2.3.3：
Hydrogenation/Hydrogenolysis / 7.3：
Hydrogenolysis of Polyols / 7.3.1：
Hydrodeoxygenation of Polyols / 7.3.2.1：
C-C Hydrogenolysis of Polyols / 7.3.2.2：
Hydrogenation of Carboxylic Acids / 7.3.3：
Levulinic Acid / 7.3.3.1：
Succinic Acid / 7.3.3.2：
Selective Hydrogenation of Furanic Compounds / 7.3.4：
Reductive Amination of Acids and Furans / 7.3.5：
Catalyst Design for the Dehydration of Biosourced Molecules / 7.4：
Glycerol to Acrolein / 7.4.1：
Lactic Acid to Acrylic Acid / 7.4.3：
Sorbitol to Isosorbide / 7.4.4：
Conclusions and Outlook / 7.5：
Conversion of Lignin to Value-added Chemicals via Oxidative Depolymerization / Justin K. Mobley8：
Cautionary Statements / 8.1：
Catalytic Systems for the Oxidative Depolymerization of Lignin / 8.2：
Enzymes and Bio-mimetic Catalysts / 8.2.1：
Cobalt Schiff Base Catalysts / 8.2.2：
Vanadium Catalysts / 8.2.3：
Methyltrioxorhenium (MTO) Catalysts / 8.2.4：
Commercial Products from Lignin / 8.3：
Stepwise Depolymerization of ß-O-4 Linkages / 8.4：
Benzylic Oxidation / 8.4.1：
Secondary Depolymerization / 8.4.2：
Heterogeneous Catalysts for Lignin Depolymerization / 8.5：
Outlook / 8.6：
Lignin Valorization via Reductive Depolymerization / Yang (Vanessa) Song9：
Late-stage Reductive Lignin Depolymerization / 9.1：
Mild Hydroprocessing / 9.2.1：
Harsh Hydroprocessing / 9.2.2：
Bifunctional Hydroprocessing / 9.2.3：
Liquid Phase Reforming / 9.2.4：
Reductive Lignin Depolymerization Using Hydrosilanes, Zinc, and Sodium / 9.2.5：
Reductive Catalytic Fractionation (RCF) / 9.3：
Reaction Conditions / 9.3.1：
Lignocellulose Source / 9.3.2：
Applied Catalyst / 9.3.3：
Acknowledgment / 9.4：
Conversion of Lipids to Biodiesel via Esterification and Transesterification / Amin Talebian-Kiakalaieh and Amin Nor Aishah Saidina10：
Different Feedstocks tor Biodiesel Production / 10.1：
Biodiesel Production / 10.3：
Algal Bio diesel Production / 10.3.1：
Nutrients for Microalgae Growth / 10.3.1.1：
Microalgae Cultivation System / 10.3.1.2：
Harvesting / 10.3.1.3：
Drying / 10.3.1.4：
Lipid Extraction / 10.3.1.5：
Catalytic Transesterification / 10.4：
Homogeneous Catalysts / 10.4.1：
Alkali Catalysts / 10.4.1.1：
Acid Catalysts / 10.4.1.2：
Two-step Esterification-Transesterification Reactions / 10.4.1.3：
Heterogeneous Catalysts / 10.4.2：
Solid Acid Catalysts / 10.4.2.1：
Solid Base Catalysts / 10.4.2.2：
Enzyme-Catalyzed Transesterification Reactions / 10.4.3：
Supercritical Transesterification Processes / 10.5：
Alternative Processes for Biodiesel Production / 10.6：
Ultrasonic Processes / 10.6.1：
Microwave-Assisted Processes / 10.6.2：
Summary / 10.7：
Upgrading of Lipids to Hydrocarbon Fuels via (Hydro)deoxygenation / David Kubicka11：
Feedstocks / 11.1：
Chemistry / 11.3：
Technologies / 11.4：
Sulfided Catalysts / 11.5：
Metallic Catalysts / 11.5.2：
Metal Carbide, Nitride, and Phosphide Catalysts / 11.5.3：
Upgrading of Lipids to Fuel-like Hydrocarbons and Terminal Olefins via Decarbonylation/Decarboxylation / Ryan Loe and Eduardo Santillan-Jimenez and Mark Crocker11.6：
Lipid Feeds / 12.1：
deCOx Catalysts: Active Phases / 12.3：
deCOx Catalysts: Support Materials / 12.4：
Reaction Mechanism / 12.5：
Catalyst Deactivation / 12.7：
Conversion of Terpenes to Chemicals and Related Products / Anne E. Harman-Ware12.8：
Terpene Biosynthesis and Structure / 13.1：
Sources of Terpenes / 13.3：
Conifers and Other Trees / 13.3.1：
Essential Oils and Other Extracts / 13.3.2：
Isolation of Terpenes / 13.4：
Tapping and Extraction / 13.4.1：
Terpenes as a By-product of Pulping Processes / 13.4.2：
Historical Uses of Raw Terpenes / 13.5：
Adhesives and Turpentine / 13.5.1：
Flavors, Fragrances, Therapeutics, and Pharmaceutical Applications / 13.5.2：
Catalytic Methods for Conversion of Terpenes to Fine Chemicals and Materials / 13.6：
Homogeneous Processes / 13.6.1：
Hydration and Oxidation Reactions / 13.6.1.1：
Homogeneous Catalysis for the Epoxidation of Monoterpenes / 13.6.1.2：
Isomerizations / 13.6.1.3：
Production of Terpene Carbonates from CO2 and Epoxides / 13.6.1.4：
Polymers and Other Materials from Terpenes / 13.6.1.5：
"Click Chemistry" Routes for the Production of Materials and Medicinal Compounds from Terpenes / 13.6.1.6：
Heterogeneous Processes / 13.6.2：
Isomerization and Hydration of ¿-Pinene / 13.6.2.1：
Heterogeneous Catalysts for the Epoxidation of Monoterpenes / 13.6.2.2：
Isomerization of ¿-Pinene Oxide / 13.6.2.3：
Vitamins from Terpenes / 13.6.2.4：
Dehydrogenation and Hydrogenation Reactions of Terpenes / 13.6.2.5：
Conversion of Terpenes to Fuels / 13.6.2.6：
Conversion of Chitin to Nitrogen-containing Chemicals / Xi Chen and Ning Yan14：
Waste Shell Biorefinery / 14.1：
Production of Amines and Amides from Chitin Biomass / 14.2：
Sugar Amines/Amides / 14.2.1：
Furanic Amines/Amides / 14.2.2：
Polyol Amines/Amides / 14.2.3：
Production of N-heterocyclic Compounds from Chitin Biomass / 14.3：
Production of Carbohydrates and Acetic Acid from Chitin Biomass / 14.4：
Production of Advanced Products from Chitin Biomass / 14.5：
Conclusion / 14.6：
Index / Eduardo Santillan-Jimenez and Mark Crocker15：
Preface
Upgrading of Biomass via Catalytic Fast Pyrolysis (CFP) / Charles A. Mullen1：
Introduction / 1.1：
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5. Plasma-material interactions in a controlled fusion reactor (: electronic bk)
Tetsuo Tanabe
出版情報: [Cham] : SpringerLink, [20--]  1 online resource (xii, 207 p.)
シリーズ名: Springer series in plasma science and technology / series editors, Michael Bonitz ... [et al.] ;
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6. Solid state chemistry in catalysis (: electronic bk)
Robert K. Grasselli, editor, James F. Brazdil, editor
出版情報: [Washington, DC] : American Chemical Society, c2022  1 online resource (365 p.)
シリーズ名: ACS symposium series ; 279
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7. Controlled radical polymerization : mechanisms (: electronic bk)
Krzysztof Matyjaszewski, editor ... [et al.] ; sponsored by the ACS Division of Polymer Chemistry
出版情報: [Washington, DC] : American Chemical Society, c2022  1 online resource (339 p.)
シリーズ名: ACS symposium series ; 1187
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8. Catalysis and the mechanism of methane conversion to chemicals : C-C and C-O bonds formation using heterogeneous, homogenous, and biological catalysts (: electronic bk)
Toshihide Baba, Akimitsu Miyaji
出版情報: [Ann Arbor, Mich.] : ProQuest Ebook Central, [20--]  1 online resource (xii, 220 p.)
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9. Nanotechnology in catalysis : applications in the chemical industry, energy development, and environment protection (: electronic bk)
edited by Bert Sels and Marcel Van de Voorde
出版情報: Wiley Online Library, 2017  1 online resource (3 v. (xxxv, 1144 p.))
シリーズ名: Nanotechnology innovation & applications
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10.

電子ブック
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10. Hydrocracking and hydrotreating : : a symposium sponsored by the Division of Petroleum Chemistry, inc., at the 169th meeting of the American Chemical Society, Philadelphia, Penn., April 9, 1975 (alk. paper)
John W. Ward, editor Shai A. Qader, editor
出版情報:   1 online resource (180 pages)
シリーズ名: ACS symposium series ; 20
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目次情報:
The Influence of Chain Length in Hydrocracking and Hydroisomerization of n-Alkanes / Catalyst Effects on Yields and Product Properties in Hydrocracking / Raffinate Hydrocracking with Palladium-Nickel-Containing Synthetic Mica-Montmorillonite Catalysts / Hydrocracking Condensed-Ring Aromatics Over Nonacidic Catalysts / Conversion of Complex Aromatic Structures to Alkylbenzenes / Diesel and Burner Fuels from Hydrocracking in Situ Shale Oil / Synthoil Process and Product Analysis / Coal Liquifaction by Rapid Gas Phase Hydrogenation / Consideration of Catalyst Pore Structure and Asphaltenic Sulfur in the Desulfurization of Resids / The Structural Form of Cobalt and Nickel Promoters in Oxidic HDS Catalysts / / WEITKAMP, JENS / SULLIVAN, R. F.; MEYER, J. A. / GIANNETTI, JOSEPH P.; FISHER, DONALD C. / WU, WEN-LUNG; HAYNES, HENRY W. / QADER, SHAIK A.; McOMBER, DAVID B. / COTTINGHAM, PHILIP L.; NICKERSON, LEO G. / STERNBERG, HEINZ W.; RAYMOND, RAPHAEL; AKHTAR, SAYEE
The Influence of Chain Length in Hydrocracking and Hydroisomerization of n-Alkanes / Catalyst Effects on Yields and Product Properties in Hydrocracking / Raffinate Hydrocracking with Palladium-Nickel-Containing Synthetic Mica-Montmorillonite Catalysts / Hydrocracking Condensed-Ring Aromatics Over Nonacidic Catalysts / Conversion of Complex Aromatic Structures to Alkylbenzenes / Diesel and Burner Fuels from Hydrocracking in Situ Shale Oil / Synthoil Process and Product Analysis / Coal Liquifaction by Rapid Gas Phase Hydrogenation / Consideration of Catalyst Pore Structure and Asphaltenic Sulfur in the Desulfurization of Resids / The Structural Form of Cobalt and Nickel Promoters in Oxidic HDS Catalysts / / WEITKAMP, JENS / SULLIVAN, R. F.; MEYER, J. A. / GIANNETTI, JOSEPH P.; FISHER, DONALD C. / WU, WEN-LUNG; HAYNES, HENRY W. / QADER, SHAIK A.; McOMBER, DAVID B. / COTTINGHAM, PHILIP L.; NICKERSON, LEO G. / STERNBERG, HEINZ W.; RAYMOND, RAPHAEL; AKHTAR, SAYEE
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