2023
DOI: 10.1021/acsomega.3c05064
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Enantioselective Synthesis of Aza-Flavanones with an All-Carbon Quaternary Stereocenter via NHC-Catalyzed Intramolecular Annulation

Izabela Barańska,
Michał Słotwiński,
Tadeusz Muzioł
et al.

Abstract: An enantioselective synthesis of functionalized azaflavanone derivatives using the N-heterocyclic carbene-catalyzed intramolecular Stetter reaction of sulphoamido benzaldehydes has been reported. This procedure presents the first original approach for synthesizing chiral functionalized flavonoids at the 3-position, containing an all-carbon quaternary stereogenic center. This advancement significantly enriches the chemical toolbox for the preparation of complex nitrogen-containing compounds and opens up new ave… Show more

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“…This presents a novel strategy for handling complex nitrogen‐containing compounds and creates exciting opportunities in organic chemical synthesis studies (Table 1). [105] …”
Section: Other Synthetic Approachesmentioning
confidence: 99%
“…This presents a novel strategy for handling complex nitrogen‐containing compounds and creates exciting opportunities in organic chemical synthesis studies (Table 1). [105] …”
Section: Other Synthetic Approachesmentioning
confidence: 99%