Contra-thermodynamic halolactonization of lactam-tethered 5-aryl-4( E )-pentenoic acids for the flexible and stereocontrolled synthesis of fused lactam-halolactones
Year: 2022
Type: article
Abstract: -methylmorpholine oxide as the catalyst. The lactam-lactone products are synthesized in high diastereoselectivity, modularity, and chemoselectivity. Notably, most of the bicycles contain one benzylic quaternary stereocenter as well as an α-alkoxy quaternary stereocenter.
Source: RSC Advances
DOI: 10.1039/d2ra04177d
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: W4308188971
