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/

Zendy Open

Presents the pdf analysis as premium feature

PDF Analysis

Insights

Presents the summarisation as premium feature

Summarisation

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the zaia usage as premium feature

ZAIA

Zendy Tools

Zendy Plus

Presents the access of premium content as premium feature

Premium Content

The full potential of a high valent metal chloride as both a chlorinating and an oxidative agent was explored by allowing WCl to react with N-(2,6-diisopropylphenyl) α-diimines, in CHCl at room temperature. These α-diimines underwent unprecedented conversion to quinoxalinium cations via intramolecular C-N coupling.

dalton transactions

Allowing the direct interaction of N-aryl α-diimines with a high valent metal chloride: one-pot WCl<sub>6</sub>-promoted formation of quinoxalinium salts

Allowing the direct interaction of N-aryl α-diimines with a high valent metal chloride: one-pot WCl6-promoted formation of quinoxalinium salts

Allowing the direct interaction of N-aryl α-diimines with a high valent metal chloride: one-pot WCl₆-promoted formation of quinoxalinium salts