Handbook of Palladium-Catalysed Organic Reactions - 1st Edition - ISBN: 9780124666153, 9780080533148

Handbook of Palladium-Catalysed Organic Reactions

1st Edition

Editors: J. Fiaud Jean-Luc Malleron J. Legros
eBook ISBN: 9780080533148
Imprint: Academic Press
Published Date: 18th February 1997
Page Count: 304
Sales tax will be calculated at check-out Price includes VAT/GST
25% off
25% off
25% off
25% off
25% off
20% off
20% off
25% off
25% off
25% off
25% off
25% off
20% off
20% off
25% off
25% off
25% off
25% off
25% off
20% off
20% off
25% off
25% off
25% off
25% off
25% off
20% off
20% off
130.00
97.50
97.50
97.50
97.50
97.50
104.00
104.00
102.00
76.50
76.50
76.50
76.50
76.50
81.60
81.60
135.00
101.25
101.25
101.25
101.25
101.25
108.00
108.00
82.00
61.50
61.50
61.50
61.50
61.50
65.60
65.60
Unavailable
Price includes VAT/GST
× DRM-Free

Easy - Download and start reading immediately. There’s no activation process to access eBooks; all eBooks are fully searchable, and enabled for copying, pasting, and printing.

Flexible - Read on multiple operating systems and devices. Easily read eBooks on smart phones, computers, or any eBook readers, including Kindle.

Open - Buy once, receive and download all available eBook formats, including PDF, EPUB, and Mobi (for Kindle).

Institutional Access

Secure Checkout

Personal information is secured with SSL technology.

Free Shipping

Free global shipping
No minimum order.

Description

This comprehensive handbook will be an indispensable research tool for chemists. Handbook of Palladium Catalysed Organic Reactions provides a synoptic description of the main types of reactions which are catalyzed by Palladium and the mechanism which causes these reactions. Each reaction is presented in graphical form and classified according to the type of transformation involved. Other books covering the use of Palladium complexes as catalysts have been written, but the Handbook is the only to offer a synoptic view, showing the catalytic cycle of each reaction. This complete coverage provides the reader with a good understanding of the parameters involved. The tables included can be viewed from the point of view of the reagents, the product of the reaction, or the mechanism involved. The Handbook is a companion to the Database of Palladium Chemistry: Reactions andCatalytic Cycles, published on CD-ROM.

Key Features

  • Begins with explicit instructions from the authors, facilitating use of the Handbook
  • Details the associated catalytic cycle for each class of reactions
  • Offers a choice of references, allowing the reader to find the closest example for solving a given problem
  • 84 types of mechanism covered, plus over 2500 references
  • Presents graphical abstracts for all reactions described, making it easy to search a type of reaction
  • Comb-bound for easy reference
  • Free demo disk included for the Database of Palladium Chemistry
  • A versatile tool for chemists in the academic community, this handbook will be an invaluable tool in the laboratory

Readership

The book is a tool for the chemist, to be used in the lab. It is aimed at the academic scientist who does not have access to the software necessary to run the CD-ROM.

Table of Contents

Abbreviations. Introduction. Graphical Abstracts of Reaction Numbers (RXN). Reactions Catalyzed by Palladium Complexes: Cross-Coupling of Organometallics with RX Derivatives. Cross-Coupling of Organometallicswith RCOX Derivatives. Cross-Coupling of Siloxycyclopropanes with RX and RCOX Derivatives. Cross-Coupling of Terminal Alkynes with RX Derivatives. Intermolecular HECK Reaction. Intramolecular HECK Reaction. Intramolecular Coupling of Di(Vinyl Halides). Tandem HECK-Anion Capture Process of Alkenes, Alkyenes, Alkynes, Allenes and Dienes. Tandem HECK-Anion Capture Process of Norbonene and Related Compounds. Tandem Arylsulfonation-Cyclization Process. Tandem Cyclization-Anion Capture (-Carbonylation) Processof Alkenes and Alkynes. Tandem Cyclization-Anion Capture (-Carbonylation) Process of Ene-Vinyl, Ene-Aryl, and Ene-Alkyl Halides. Tandem Cyclization-Anion Capture Process of Yne-Vinyl and Yne-Aryl Halides. Hydroarylation and Hydrovinylation of Alkenes andAlkynes. Reduction of Alkenes. Semihydrogenation of Alkynes and 1,3-Dienes. Hydroboration, Hydrogennyladon, Hydrosilylation and Hydrostannation of Alkynes, Allenes, Dienes, and Enynes. Hydroselenation of Alkynes. 1,4-Disilyation of Conjugated Enones. Hydrocarboxylation, Hydrocarboalkoxylation and Hydrocarboamination of Alkenes and Alkynes. Tandem Carbonylation-Arylation with Alkynes. 1,2-Dimetallation of Alkynes and Alkenes and Related Reactions. 1,2-Dimetallation of Isonitriles. 1,2-Dimetallation of Allenes. Coupling of Aryl Derivatives with Alkenes Involving a Pd(II) Catalyst. Homocoupling of Aryl and Vinyl Derivatives. Codimerization of Alkynes. Codimerization of Terminal Alkynes with Allenes. Codimerization of Alkynes and Allyl Halides. Cyclopropanation of Alkenes and 1,3-Dienes by Diazomethane. Rearrangement of (-Hydroxy Diazo Compounds. Substitution, Addition, and Elimination on Pro-(-Allyl Substrates. [3,3]-Sigmatropic Rearrangement and [1,3]-Shift on Allylic Derivatives. 1,3-Diene Monoepoxide Rearrangement. Ring Extension of Cyclobutane Derivatives. [3+2], [3+4], [3+6], [1+2] Cycloadditions. Intramolecular Ene-Like Reactions. Cyclization of Hexatrienolate Derivatives. Amination or Amidation of Alkenes. Alkoxylation of Alkenes and Alkynes. Acetalization of Alkenes. Allylic Acyloxylation of Cycloalkenes. Tandem Acyloxylation-Cyclization of 1,5-Dienes. Tandem Acycloxychlorination-Cyclization of 1,6-Dienes. 1,4-Acycloxychlorination of 1,3-Dienes. 1,4-Diacyloxylation of 1,3-Dienes and Related Reactions. Intramolecular Amination, Alkoxylation of Acyloxylation of Alkynes. Tandem Intramolecular Amination, Alkoxylation, or Acyloxylation-Allylation of Alkynes and Allenes. Tandem Intramolecular Amination, Alkoxylation, or Acyloxylation-Carbonylation of Alkynes. Intramolecular Amination or Alkoxylation of Alkenes. Tandem Intramolecular Amination or Alkoxylation-Carbonylation of Alkenes and Allenes. Reductive Cyclization with Diynes and Enynes. Cycloisomerization of Diynes and Enynes. Cycloaddition of Aziridines with Carbodiimides. Telomerization of 1,3-Dienes with Nucleophiles. WACKER Process. Preparation of Ketones from Alcohols or Derivatives via a (-Hydride Elimination. Preparation of ((-Unsaturated Carbonyl Derivatives via a (-Hydride Elimination. Preparation of (-Diketones Derivatives via an Oxidative Rearrangement of a Propargyl Acetate. Carbonylation. Isomerization of Alkynes. Addition of Thiols to Alkynes. Preparation of Allylic Acetates from Alkynes by Tandem Redox-Addition. Tandem Cyclization-Capture Process of Enynes. Aldol-Like Condensation of Enol Esters with Aldehydes. Addition of Fluoroalkyl Iodides to Alkenes or Alkynes via a Pd(I) Species. Intermolecular Tandem Carbonylation-Coupling-Cyclization Process of Aryl Halides with Terminal Alkynes.Intramolecular Coupling of Aryl Halides with Arenes. Tandem Intramolecular Alkoxylation-Vinylation of Alkenes. Carbonylative [2+2] Cycloaddition. Dicarboalkoxylation of Alkenes. Addition of Pronucleophiles on 1,3-Dienes or Allenes. Tandem Cycloisomerization-Cycloaddition of Dienynes with 1,3-Dienes via Metallodienes. Acylcyanation of Terminal Alkynes. 1,4-Carbochlorination of 1,3-Dienes. Tandem Chlorination-Cyclization and Tandem Chlorination-Carbonylation-Cyclization of 1,6-Enynes. Intramolecular Cyclocarbonylation of Alkenes. Abbreviations and Symbols. Notes. Subject Index.

Details

No. of pages:
304
Language:
English
Copyright:
© Academic Press 1997
Published:
Imprint:
Academic Press
eBook ISBN:
9780080533148

About the Editor

J. Fiaud

Affiliations and Expertise

Universite Paris-Sud Orsay,France

Jean-Luc Malleron

Jean-Luc Malleron received his graduate degree from the school of chemistry at Montpellier and then went on to obtain his Ph.D. at the Université Paris Sud. Malleron has been Senior Research Fellow in medicinal chemistry at Rhône-Poulec Rorer Company since 1981.

Affiliations and Expertise

Rhône-Poulenc Rorer, France

J. Legros

Affiliations and Expertise

Universite Paris-Sud Orsay, France

Ratings and Reviews