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

Dichlorotetrazolo(1,5-a)pyridine/2-azido-3,5-dichloropyridine 3 undergoes a slow reaction with dialkylamines (R = ethyl or propyl) in the dark at room temperature to afford 2- pyridylformamidines 8, which on chromatography on silica gel hydrolyse to afford the formamide 9.

N,N-Dialkyl-N '-(2-pyridyl)formamidines and N-(3,5-dichloro-2-pyridyl)formamide. Reactions of tetrazolopyridines with nucleophiles, part 1