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

A Model Study for the Total Synthesis of Lophotoxin

Photo from archive.org

Abstract A concise synthetic approach to construct [6] , [6] , [6] -tricyclic core, bearing 14-membered carbocyclic skeleton and oxygen at C13 of lophotoxin, has been described. This approach features… Click to show full abstract

Abstract A concise synthetic approach to construct [6] , [6] , [6] -tricyclic core, bearing 14-membered carbocyclic skeleton and oxygen at C13 of lophotoxin, has been described. This approach features a diastereoselective intermolecular Diels−Alder furan reaction and intramolecular Michael reaction. N-methylmaleimide was found to be critical for achieving the stable intermolecular Diels−Alder furan outcome.

Keywords: lophotoxin; model study; synthesis lophotoxin; total synthesis; study total

Journal Title: Tetrahedron Letters
Year Published: 2021

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.