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

Ferrocene reacts with an excess of boron triiodide or boron tribromide in hexane solution to give mixtures of 1,3,1′-tris- and 1,3,1′,3′-tetrakis- (dihalogenoboryl)ferrocene. The borylation proceeds stepwise, the intermediates being essentially the known dihalogenoborylferrocene and 1,1′-bis- (dihalogenoboryl)ferrocene compounds, although small am ounts of 1,3-bis(dihalogenoboryl)- ferrocene can also be identified.  1 H,  11 B and  13 C NMR data are given.

Notizen: Zur Synthese mehrfach borylierter Ferrocene/Synthesis of Polyborylated Ferrocenes