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The Resource Sustainable catalysis, Part 2, Without metals or other endangered elements, editor: Michael North

Sustainable catalysis, Part 2, Without metals or other endangered elements, editor: Michael North

Label
Sustainable catalysis, Part 2, Without metals or other endangered elements
Title
Sustainable catalysis
Title number
Part 2
Title part
Without metals or other endangered elements
Statement of responsibility
editor: Michael North
Title variation
Without metals or other endangered elements
Contributor
Editor
Subject
Language
eng
Summary
Catalysis is a fundamentally sustainable process which can be used to produce a wide range of chemicals and their intermediates. Focussing on those catalytic processes which offer the most sustainability, this two-part book explores recent developments in this field, as well as examining future challenges. Focussing on catalysis without metals or other endangered elements, each chapter covers a different type of organocatalyst. Beginning with chapters on acid and base catalysis, the book then concentrates on asymmetric catalysis. Several chapters cover pyrrolidine-based and cinchona alkaloid-based catalysts, whilst other chapters examine further organoctalysts which are constructed only from sustainable elements. Together with Sustainable Catalysis: With Non-endangered Metals, these books examine the progress in sustainable catalysis in all areas of chemistry, and are an important reference for researchers working in catalysis and green chemistry
Member of
Cataloging source
UKRSC
Index
index present
Language note
English
Literary form
non fiction
Nature of contents
  • dictionaries
  • bibliography
Series statement
RSC green chemistry
Series volume
41
Sustainable catalysis, Part 2, Without metals or other endangered elements, editor: Michael North
Label
Sustainable catalysis, Part 2, Without metals or other endangered elements, editor: Michael North
Link
http://libproxy.rpi.edu/login?url=http://app.knovel.com/hotlink/toc/id:kpSCWMOE0A/sustainable-catalysis-without
Publication
Copyright
Note
Includes index
Related Contributor
Related Location
Related Agents
Related Authorities
Related Subjects
Related Items
Antecedent source
unknown
Bibliography note
Includes bibliographical references at the end of each chapters and index
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
  • Cover; Contents; Preface; References; Part 2; Chapter 14 Nonquaternised Cinchona Alkaloid Derivatives as Asymmetric Organocatalysts for Carbon-Carbon Bond-forming Reactions ; 14.1 Introduction; 14.2 Catalytic Asymmetric 1,4-Addition Reactions; 14.3 Catalytic Asymmetric 1,2-Addition Reactions; 14.4 Catalytic Asymmetric Cycloaddition Reactions; 14.5 Concluding Remarks; References; Chapter 15 Nonquaternised Cinchona Alkaloid Derivatives as Asymmetric Organocatalysts for Carbon-Heteroatom Bond-forming Reactions ; 15.1 Introduction; 15.2 Hydrophosphonylation; 15.3 Epoxidation and Hydroperoxidation
  • 16.2.1 Monoalkylation of Schiff Bases Derived from Glycine16.2.2 Dialkylation of Schiff Bases Derived from Glycine; 16.2.3 Other Alkylations with Cinchona-derived PTC Catalysts; 16.2.4 Conjugate Additions with Cinchona-derived PTC Catalysts; 16.2.5 Aldol Reactions with Cinchona-derived PTC Catalysts; 16.2.6 Mannich Reactions with Cinchona-derived PTC Catalysts; 16.2.7 Darzens Reaction with Cinchona-derived PTC Catalysts; 16.2.8 Epoxidation of Enones with Cinchona-derived PTC Catalysts; 16.2.9 Other Reactions with Cinchona-derived PTC Catalysts; 16.3 Conclusions; References
  • Chapter 17 Binaphthyl-derived Cyclic Amines and Their Salts as Asymmetric Organocatalysts 17.1 Introduction; 17.2 Design of Chiral Amine Catalysts; 17.2.1 Aldol Reactions; 17.2.2 Mannich Reactions; 17.2.3 Conjugate Additions; 17.2.4 C-O and C-N Bond Formations; 17.2.5 Halogenations; 17.3 Design of Chiral Phase-transfer Catalysts; 17.3.1 Alkylations; 17.3.2 Conjugate Additions; 17.3.3 Aldol and Mannich Reactions; 17.3.4 Strecker Reactions; 17.3.5 Oxidations; 17.4 Conclusions; References; Chapter 18 Imidazolidinones as Asymmetric Organocatalysts ; 18.1 Introduction
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Dimensions
unknown
http://library.link/vocab/discovery_link
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Extent
1 online resource.
File format
unknown
Form of item
online
Isbn
9781782626435
Level of compression
unknown
Media category
computer
Media MARC source
rdamedia
Media type code
c
Quality assurance targets
not applicable
Reformatting quality
unknown
Sound
unknown sound
Specific material designation
remote

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