
Multicomponent Reactions, Volume 2
Reactions Involving an a,ß-Unsaturated Carbonyl Compound as Electrophilic Compon
Thieme (Publisher)
1st Edition
Published on 27. November 2013
Book
Hardback
626 pages
978-3-13-172831-9 (ISBN)
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Description
The two volumes "Science of Synthesis: Multicomponent Reactions" critically review the state of the art of domino, sequential, and consecutive multicomponent reactions in what is a highly dynamic field. They serve as the basis for practical application to reach the goals of diversity-oriented synthesis, reaction design, and novel synthetic concepts. As is typical for the Science of Synthesis series, the reference work on multicomponent reactions presents the best synthetic methods as judged by experts in the field and includes typical and general experimental procedures.The volume "Reactions Involving an alpha,beta-Unsaturated Carbonyl Compound as Electrophilic Component" covers the following topics:Michael Additions Wittig ReactionsCycloadditionsReactions Involving an alpha,beta-Unsaturated Carbonyl Compound as Electrophilic Component with Electron-Deficient Alkynes as Electrophiles Reactions with Cycloaddition as the Key Step Boron-Mediated Multicomponent Reactions Silicon-Mediated Multicomponent Reactions Free-Radical Mediated Multicomponent Reactions Metal-Mediated Multicomponent Reactions
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Series
Edition
1. Auflage
Language
English
Place of publication
Stuttgart
Germany
Target group
Professional and scholarly
Wissenschaftler
Edition type
New edition
Illustrations
0 Abbildungen
Dimensions
Height: 24 cm
Width: 17 cm
Weight
454 gr
ISBN-13
978-3-13-172831-9 (9783131728319)
Schweitzer Classification
Other editions
Additional editions

Multicomponent Reactions, Volume 2
Reactions Involving an a,ß-Unsaturated Carbonyl Compound as Electrophilic Compon
Book
03/2014
1st Edition
Thieme
€259.99
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Content
2.1 Reactions Involving an ?,?-Unsaturated Carbonyl Compound or Analogue as Electrophilic Component
2.1.1 Michael Addition as the Key Step
2.1.2 In Situ Generation of the ?,?-Unsaturated Carbonyl Component by Wittig-Type Reaction
2.1.3 With Isocyanide Participation
2.1.4 Electron-Deficient Alkynes as Electrophiles
2.1.5 [2+2] Cycloaddition as the Key Step
2.1.6 [3+2] Cycloaddition as the Key Step
2.1.7 [4+2] Cycloaddition as the Key Step
2.2 Reactions with Cycloaddition as the Key Step (Not Involving ?,?-Unsaturated Carbonyl Compound Electrophiles)
2.2.1 [3+2] Cycloaddition
2.2.2 [4+2] Cycloaddition
2.3 Boron-Mediated Multicomponent Reactions
2.4 Silicon-Mediated Multicomponent Reactions
2.5 Free-Radical-Mediated Multicomponent Reactions Involving Carbon Monoxide
2.6 Metal-Mediated Multicomponent Reactions
2.6.1 Stoichiometric Metal Participation
2.6.2 Catalytic Metal Participation
2.1.1 Michael Addition as the Key Step
2.1.2 In Situ Generation of the ?,?-Unsaturated Carbonyl Component by Wittig-Type Reaction
2.1.3 With Isocyanide Participation
2.1.4 Electron-Deficient Alkynes as Electrophiles
2.1.5 [2+2] Cycloaddition as the Key Step
2.1.6 [3+2] Cycloaddition as the Key Step
2.1.7 [4+2] Cycloaddition as the Key Step
2.2 Reactions with Cycloaddition as the Key Step (Not Involving ?,?-Unsaturated Carbonyl Compound Electrophiles)
2.2.1 [3+2] Cycloaddition
2.2.2 [4+2] Cycloaddition
2.3 Boron-Mediated Multicomponent Reactions
2.4 Silicon-Mediated Multicomponent Reactions
2.5 Free-Radical-Mediated Multicomponent Reactions Involving Carbon Monoxide
2.6 Metal-Mediated Multicomponent Reactions
2.6.1 Stoichiometric Metal Participation
2.6.2 Catalytic Metal Participation