Alkyl Aryl Ether Bond Formation with PhenoFluor

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

doi:10.1002/anie.201500902

アイテム詳細

登録内容を編集ファイル形式で保存

一時保存へ追加

タグ情報を表示リリース履歴を表示詳細要約

公開

学術論文

Alkyl Aryl Ether Bond Formation with PhenoFluor

MPS-Authors

There are no MPG-Authors in the publication available

External Resource

There are no locators available

Fulltext (restricted access)

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

フルテキスト (公開)

公開されているフルテキストはありません

付随資料 (公開)

There is no public supplementary material available

引用

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.

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

要旨

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.