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

Cobalt-Catalyzed Regio-, Diastereo-, and Enantioselective Reductive Coupling of Internal Alkynes with Cyclobutenes.

Herein, we report the cobalt-catalyzed asymmetric ene-yne reductive coupling of internal alkynes and unactivated cyclobutenes. The reaction produced densely functionalized chiral vinyl cyclobutanes in up to 92% yields with excellent… Click to show full abstract

Herein, we report the cobalt-catalyzed asymmetric ene-yne reductive coupling of internal alkynes and unactivated cyclobutenes. The reaction produced densely functionalized chiral vinyl cyclobutanes in up to 92% yields with excellent absolute and relative stereocontrol (>99% ee, >20:1 dr, and >20:1 E/Z), and high >20:1 regioselectivity. The scaled-up reaction and the postsynthetic derivatizations further elucidated the efficiency of the designed protocol. The preliminary mechanistic investigations suggested the involvement of zinc-mediated low-valent cobalt(I) complex generation, oxidative ene-yne cyclization, and protonation as the key mechanistic steps.

Keywords: catalyzed regio; coupling internal; reductive coupling; cobalt catalyzed; regio diastereo; internal alkynes

Journal Title: Organic letters
Year Published: 2025

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.