Alkyl Aryl Ether Bond Formation with PhenoFluor | Zendy

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

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Alkyl Aryl Ether Bond Formation with PhenoFluor

Author(s) -

Shen Xiao,

Neumann Constanze N.,

Kleinlein Claudia,

Goldberg Nathaniel W.,

Ritter Tobias

Publication year - 2015

Publication title -

angewandte chemie

Language(s) - English

Resource type - Journals

eISSN - 1521-3757

pISSN - 0044-8249

DOI - 10.1002/ange.201500902

Subject(s) - ether , aryl , chemistry , alkyl , reactivity (psychology) , williamson ether synthesis , primary (astronomy) , phenols , substrate (aquarium) , organic chemistry , medicine , oceanography , pathology , astronomy , geology , alternative medicine , physics

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.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research