LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Catalytic asymmetric synthesis of medium-sized bridged biaryls.

Photo by courtneywentz from unsplash

Despite the persistent presence of medium-sized (seven- to nine-membered) scaffolds in natural products and biologically active molecules, their asymmetric syntheses have always been considered a formidable task; therefore, they have… Click to show full abstract

Despite the persistent presence of medium-sized (seven- to nine-membered) scaffolds in natural products and biologically active molecules, their asymmetric syntheses have always been considered a formidable task; therefore, they have remained underdeveloped when compared to the enantioselective synthesis of five- and six-membered ring scaffolds. One important class of such medium-sized ring frameworks includes seven- to nine-membered biaryl bridged carbo- and heterocycles. These medium-ring-sized biaryl frameworks possess more configurational stability than the related smaller ring structures and are common features of valuable natural products, bioactive compounds, chiral catalysts, and molecular motors. Due to these exciting properties and broad applications, over the last few years, the catalytic enantioselective synthesis of medium-sized bridged biaryls has seen an upsurge. This highlight article describes the development of organocatalysed and transition-metal catalysed transformations for procuring seven-, eight-, and nine-membered bridged biaryls bearing a chiral axis/one or more asymmetric carbon centres.

Keywords: synthesis medium; medium sized; medium; bridged biaryls; sized bridged

Journal Title: Chemical communications
Year Published: 2022

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.