Site-selective, catalytic, and diastereoselective sp 3 C–H hydroxylation and alkoxylation of vicinally functionalized lactams
Year: 2020
Type: article
Abstract: C-H hydroxylation/alkoxylation protocols featuring dihydroisoquinolones, γ-, and δ-lactams, which bear vicinal stereocenters. The hydroxylation strategy utilizes oxygen, a waste-free oxidant and affords attractive fragments for potential drug discovery. Fe-catalyzed dehydrative coupling of the resulting tertiary alcohols with simple primary alcohols has led to the construction of highly versatile unsymmetrical dialkyl ethers.
Source: RSC Advances
DOI: 10.1039/d0ra03726e
Authors: Timothy K. Beng, Victoria Shearer, Rachel Davey, Ivianne Redman
Institution: Central Washington University
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $1,042
Funder: Central Washington University
OpenAlex ID: W3031984423
