Palladium‐Catalyzed Carboetherification and Carboamination Reactions of γ‐Hydroxy‐ and γ‐Aminoalkenes for the Synthesis of Tetrahydrofurans and Pyrrolidines
Top Cited Papers
- 10 January 2007
- journal article
- review article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2007 (4) , 571-582
- https://doi.org/10.1002/ejoc.200600767
Abstract
Substituted tetrahydrofuran and pyrrolidine moieties are displayed in a wide range of interesting biologically active molecules. The Pd‐catalyzed carboetherification or carboamination of γ‐hydroxy and γ‐aminoalkenes is a powerful tool for the construction of these heterocycles, as it is convergent and can allow access to a variety of analogs from a single γ‐hydroxy‐ or γ‐aminoalkene starting material. This microreview describes the current state of this field. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)Keywords
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