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

Both steric repulsion and electronic effect govern the stereoselectivity in asymmetric catalysis. Rationally electronic-tuned N -(2-hydroxylphenyl)-(S)-prolinamide derived catalysts were designed, synthesized, and evaluated in the asymmetric aldol reaction. The results indicate that the enantiomeric ratios of products correlate well with the Hammett constants, which confirms that the enantioselectivity was improved via rationally tuning catalyst electronic effects.

Improving enantioselectivity via rationally tuning electronic effect of catalysts in the organocatalytic asymmetric aldol reaction