cs3c04631_si_001.pdf (14.38 MB)
Harnessing NHC/Base-Catalyzed Regiodivergent Oxidative Cyclization for Versatile Aminolactone Synthesis
journal contributionposted on 2023-11-28, 13:07 authored by In-Seok Choi, Phil-Sik Kim, Wonbin Ha, Young Ho Kim, Huen Ji Yoo, Jeonghyo Lee, So Won Youn
A regiodivergent oxidative cyclization of ynamide-tethered benzaldehydes has been achieved using an organocatalytic approach based on NHC/base. The method enables the efficient synthesis of aminolactones with high regioselectivity, including the formation of 5-exo products through umpolung β-addition of ynamides. The reaction involves NHC-catalyzed aerobic oxidation of the benzaldehyde moiety followed by cyclization toward the ynamide. Computational and experimental studies have shed light on the significance of proton dissociation from the in situ generated carboxylic acid in determining the regioselectivity of the reaction. The synthetic versatility and value of aminolactones obtained from this method are also highlighted.
organocatalytic approach basedgenerated carboxylic acidcatalyzed aerobic oxidationbenzaldehyde moiety followedversatile aminolactone synthesisregiodivergent oxidative cyclizationreaction involves nhcefficient synthesiscyclization towardumpolung βtethered benzaldehydessynthetic versatilitysitu shed lightproton dissociationharnessing nhcexperimental studiesexo also highlightedachieved using5 -<