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 Plus monthly

Global: Zendy Tools annual

Global: Zendy Tools monthly

Global: Zendy Free Plan

The synthesis of racemic (5 R* ,6 R* )-6-(3-( tert -Butyldimethylsilyloxy)prop-1-ynyl)-5-hydroxypiperidin-2-one was accomplished in 10.3% overall yield over 7 steps. The key steps involved a Sonogashira coupling reaction to make an ene-yne ester and an azidolysis reaction of an epoxide ester to form a γ-lactone.

SYNTHESIS OF (5R*,6R*)-6-(3-(TERT-BUTYLDIMETHYLSILYLOXY)PROP-1-YNYL)-5-HYDROXYPIPERIDIN-2-ONE.

SYNTHESIS OF (5R,6R)-6-(3-(TERT-BUTYLDIMETHYLSILYLOXY)PROP-1-YNYL)-5-HYDROXYPIPERIDIN-2-ONE.