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

Various diaryl/hetaryl representatives of penta-1,4-dien-3-one series attract the attention of synthetic chemists during several decades owing to the possibility of their consequent chemical modification resulted in obtaining compounds of potential interest to materials science. In addition to their synthetic importance, title diarylideneacetones can be applied directly as medical drugs, such as antioxidants and anti-inflammatory agents. In this communication, we report the synthesis of a series of new asymmetric thiazole cycle containing diarylideneacetones, which further demonstrated high regioselectivity in their reaction with hydrazine. To clarify this feature, quantum-chemical modeling of the cyclization process was conducted.

Novel Asymmetric Thiazolyl-Substituted Penta-1,4-Dien-3-Ones and 3,5-Diaryl-2-Pyrazolines