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

Dioximes of 1,6-heptanediones from acetylene and ketones: only three atom-economic steps

Photo by vlisidis from unsplash

2-Acetyl-3,4-dihydropyrans, synthesized from acetylene and ketones in two steps, react with hydroxylamine to afford 5-hydroxy-1,6-heptanedione dioximes (E,E-isomers) in 72–96% yields. Click to show full abstract

2-Acetyl-3,4-dihydropyrans, synthesized from acetylene and ketones in two steps, react with hydroxylamine to afford 5-hydroxy-1,6-heptanedione dioximes (E,E-isomers) in 72–96% yields.

Keywords: acetylene ketones; three atom; ketones three; dioximes heptanediones; atom economic; heptanediones acetylene

Journal Title: Mendeleev Communications
Year Published: 2018

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.