Alkyl Aryl Ether Bond Formation with PhenoFluor

Shen, Xiao; Neumann, Constanze N.; Kleinlein, Claudia; Goldberg, Nathaniel W.; Ritter, Tobias

doi:10.1002/anie.201500902

Item

ITEM ACTIONSEXPORT

Add to Basket

Local TagsRelease HistoryDetailsSummary

Released

Journal Article

Alkyl Aryl Ether Bond Formation with PhenoFluor

MPS-Authors

There are no MPG-Authors in the publication available

External Resource

No external resources are shared

Fulltext (restricted access)

There are currently no full texts shared for your IP range.

Fulltext (public)

There are no public fulltexts stored in PuRe

Supplementary Material (public)

There is no public supplementary material available

Citation

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.

Cite as: https://hdl.handle.net/11858/00-001M-0000-002B-84B8-C

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.