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/

Zendy Plus

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

Zendy Tools

Zendy Open

Dioxoruthenium(VI) porphyrins including those containing chiral porphyrinato ligands can be readily prepared by oxidation of (RuII(Por)(CO)(MeOH)) with PhIO or meta- chloroperoxybenzoic acid. Similar reactions with PhINTs gave (RuVI(Por)(NTs)2) isolated as air stable solids at room temperature. The (RuVI(Por)O2) complexes are competent oxidants for epoxidation of alkenes with high selectivities. Enantioselective epoxidation of alkenes giving the corresponding organic epoxides with moderate to good enantioselectivites have also been achieved using chiral (RuVI(D4-Por*)O2 )( D4-H2Por* º 5,10,15,20-tetrakis-(1S,4R,5R,8S- 1,2,3,4,5,6,7,8-octahydro-1,4:5,8-dimethanoanthracen-9-yl)porphyrin) and (Ru VI(D2-Por*)O2) complexes. The mechanism of alkene epoxidation by (RuVI(Por)O2) has been examined. Procedures for catalytic epoxidation of alkenes using ruthenium porphyrin catalysts has also been developed. (RuVI(Por)(NTs)2) was found to undergo aziridination of alkenes and amidation

Ruthenium-oxo and -tosylimido porphyrin complexes for epoxidation and aziridination of alkenes