
Green Synthesis and Catalysis, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 1, 2024
Language: Английский
Green Synthesis and Catalysis, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 1, 2024
Language: Английский
The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(5), P. 3365 - 3382
Published: Feb. 16, 2024
A tunable cascade reaction of ureidomalonates and alkenyl azlactones was disclosed, which gave rise to the construction N-aroyl α-amino acid ester imide-functionalized hydantoins in moderate good yields with excellent diastereoselectivities. The pathway precisely manipulated by organocatalysis phase-transfer/sunlight relay catalysis, respectively, realize divergent synthesis. successful gram-scale preparation representative products exhibited application potential this protocol. Mechanistic studies indicated that exchange phase transfer ethoxy anion played a key role altering pathway, sunlight might accelerate oxidation process at late stage triggered phase-transfer catalysis.
Language: Английский
Citations
1Angewandte Chemie, Journal Year: 2024, Volume and Issue: 136(25)
Published: April 9, 2024
Abstract Cascade radical cyclization constitutes an atom‐ and step‐economic route for rapid assembly of polycyclic molecular skeletons. Although array redox‐active metal catalysts has recently shown robust applications in enabling various catalytic cascade processes, the use free organic as catalyst, which is capable triggering strategically distinct cascades, rarely been developed. Here, we disclosed that benzimidazolium‐based N ‐heterocyclic carbene (NHC)‐boryl catalyzing reactions both intra‐ intermolecular pathways, assembling [5,5] fused bicyclic [6,6,6] tricyclic molecules, respectively. The start with chemo‐ regioselective addition boryl catalyst to a tethered alkene or alkyne moiety, followed by either intramolecular formal [3+2] [2+2+2] cycloaddition process construct bicyclo[3.3.0]octane tetrahydrophenanthridine skeletons, Eventually, β‐elimination occurs release completing cycle. High excellent diastereoselectivity achieved under substrate control.
Language: Английский
Citations
1Journal of Organometallic Chemistry, Journal Year: 2024, Volume and Issue: 1016, P. 123235 - 123235
Published: June 16, 2024
Language: Английский
Citations
1Bioorganic Chemistry, Journal Year: 2024, Volume and Issue: 151, P. 107694 - 107694
Published: Aug. 5, 2024
Language: Английский
Citations
1Green Synthesis and Catalysis, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 1, 2024
Language: Английский
Citations
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