English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

catalyzed reaction of epoxides with isocyanates, sometimes referred to as “1,3-cycloaddition,” in fact proceeds in three steps including halide opening of the epoxide ring; resulting alkoxide reacting with the isocyanate; and the carbamate anion displacing the halide in a ring-closing reaction. The three-step sequence yields oxazolidinone product with a catalytic amount of the halide and no other products are formed. 15 The overall synthetic strategy of oxazolidinone antibacterials would then follow a modular approach consisting of three operations: the 1,3-cycloaddition of glycidyl tosylate and p-bromoaryl isocyanates; the replacement of the tosylate followed by subsequent transformations for the “C5 substituent”; and the replacement of the para-bromine by

Glycidyl Tosylate is a Viable Starting Material for Oxazolidinone Antibacterials