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

o-Quinone methide with overcrowded olefinic core as a catalytically-active surrogate of triarylmethylium salt for dehydridative oxidation of benzylic alcohols under aerobic photoirradiation conditions

Photo by unstable_affliction from unsplash

Abstract An o-quinone methide (o-QM) competent as a catalyst for the dehydridative oxidation of benzylic alcohols was developed. The introduction of an overcrowded olefinic component into the o-QM induced structural… Click to show full abstract

Abstract An o-quinone methide (o-QM) competent as a catalyst for the dehydridative oxidation of benzylic alcohols was developed. The introduction of an overcrowded olefinic component into the o-QM induced structural distortion, beneficial for imparting triarylmethylium character and regenerability. The zwitterionc resonance form of the o-QM, generated via photoexcitation and subsequent relaxation, exerted the dehydridation activity. Density functional theory calculations were conducted to gain insights into the operative catalytic process.

Keywords: quinone methide; dehydridative oxidation; oxidation benzylic; benzylic alcohols; overcrowded olefinic

Journal Title: Tetrahedron
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.