SO2F2-mediated transformation of 2'-hydroxyacetophenones to benzo-oxetes

A catalyst-free novel and efficient methodology for the challenging synthesis of benzo-oxetes from 2'-hydroxyacetophenones mediated by sulfuryl fluoride (SO2F2) gas has been realized. The combination of 2'-hydroxyacetophenones and SO2F2 furnishes synthetically challenging benzo-oxetanes in...

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Bibliographic Details
Main Authors: Revathi Lekkala, Ravindar Lekkala, Balakrishna Moku, K. P. Rakesh, Hua-Li Qin
Format: Article
Language:English
Published: Beilstein-Institut 2019-04-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.15.95
Description
Summary:A catalyst-free novel and efficient methodology for the challenging synthesis of benzo-oxetes from 2'-hydroxyacetophenones mediated by sulfuryl fluoride (SO2F2) gas has been realized. The combination of 2'-hydroxyacetophenones and SO2F2 furnishes synthetically challenging benzo-oxetanes in moderate to excellent yields. The highlight of this work is the design and synthesis of strained four-membered oxete rings.
ISSN:1860-5397