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Palladium‐Catalyzed Carboetherification and Carboamination Reactions of γ‐Hydroxy‐ and γ‐Aminoalkenes for the Synthesis of Tetrahydrofurans and Pyrrolidines

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Wolfe, John P.·2007·European Journal of Organic Chemistry

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)

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Metadata

Authors
Wolfe, J. P.
Venue
European Journal of Organic Chemistry
Publisher
Wiley
Published
2007-01-10
Volume
2007
Issue
4
Pages
571-582
ISSN
  • 1099-0690 (ISSN-L)
  • 1434-193X
OpenAlex
W2002839308
Cited by
241
References
0
FWCI
8.57
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Palladium‐Catalyzed Carboetherification and Carboamination Reactions of γ‐Hydroxy‐ and γ‐Aminoalkenes for the Synthesis of Tetrahydrofurans and Pyrrolidines. https://app.cochat.ai/papers/10.1002/ejoc.200600767
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Wolfe, J. P. (2007). Palladium‐Catalyzed Carboetherification and Carboamination Reactions of γ‐Hydroxy‐ and γ‐Aminoalkenes for the Synthesis of Tetrahydrofurans and Pyrrolidines. European Journal of Organic Chemistry. https://doi.org/10.1002/ejoc.200600767

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