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

The intramolecular hetero- Diels–Alder reaction of an aryl imino ether (diene) with an aryl nitrile (dienophile) has been used as the key reaction in an efficient approach to the pyrroquinazolino-quinoline alkaloid, luotonin A. Activation of the diene moiety by the incorporation of a methoxy group played an important role for the hetero Diels–Alder reaction.

An efficient total synthesis of the pyrroquinazolinoquinoline alkaloid, Luotonin A, employing an intramolecular hetero Diels–Alder reaction