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  Alkyl Aryl Ether Bond Formation with PhenoFluor

Shen, X., Neumann, C. N., Kleinlein, C., Goldberg, N. W., & Ritter, T. (2015). Alkyl Aryl Ether Bond Formation with PhenoFluor. Angewandte Chemie International Edition, 54(19), 5662-5665. doi:10.1002/anie.201500902.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002B-84B8-C Version Permalink: https://hdl.handle.net/21.11116/0000-0008-DBA9-3
Genre: Journal Article

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 Creators:
Shen, Xiao1, Author
Neumann, Constanze N.1, Author           
Kleinlein, Claudia1, Author
Goldberg, Nathaniel W.1, Author
Ritter, Tobias1, Author           
Affiliations:
1Department for Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA, ou_persistent22              

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Free keywords: alkyl aryl ethers; C-O bond formation; fluorine; Mitsunobu reaction; PhenoFluor
 Abstract: An alkyl aryl ether bond formation reaction between phenols and primary and secondary alcohols with PhenoFluor has been developed. The reaction features a broad substrate scope and tolerates many functional groups, and substrates that are challenging for more conventional ether bond forming processes may be coupled. A preliminary mechanistic study indicates reactivity distinct from conventional ether bond formation.

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Language(s): eng - English
 Dates: 2015-01-302015-03-202015-05-04
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/anie.201500902
 Degree: -

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Title: Angewandte Chemie International Edition
  Abbreviation : Angew. Chem., Int. Ed.
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 54 (19) Sequence Number: - Start / End Page: 5662 - 5665 Identifier: ISSN: 1433-7851
CoNE: https://pure.mpg.de/cone/journals/resource/1433-7851