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Palladium-Catalyzed Heck-Type Coupling of Allyl Esters: β-Hydride versus β-Acetoxy Elimination
Abstract This account presents recent progress in palladium-catalyzed Heck-type reactions of allyl esters with aryl halides, arylmetallic reagents, or arenes. Many improvements have been achieved to control the regioselectivity of β-hydride or β-acetoxy elimination. 1 Introduction 2 Palladium-Catal...
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Published in: | Synlett 2010-07, Vol.2010 (11), p.1577-1588 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract
This account presents recent progress in palladium-catalyzed
Heck-type reactions of allyl esters with aryl halides, arylmetallic
reagents, or arenes. Many improvements have been achieved to control
the regioselectivity of β-hydride or β-acetoxy elimination.
1 Introduction
2 Palladium-Catalyzed Heck-Type Coupling of Allyl Esters with
Aryl Halides
3 Palladium-Catalyzed Heck-Type Coupling of Allyl Esters with
Organometallic Reagents
4 Palladium-Catalyzed Heck-Type Coupling of Allyl Esters with
Arenes via Aromatic C-H Activation
5 Other Transition Metal Catalyzed Heck-Type Reactions of Allyl
Esters
6 Conclusion |
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ISSN: | 0936-5214 1437-2096 |
DOI: | 10.1055/s-0030-1258083 |