Advanced green synthesis: Solvent-free and catalyst-free reaction DOI Creative Commons
Mengyao Li,

Ao Gu,

Jiatong Li

et al.

Green Synthesis and Catalysis, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 1, 2024

Language: Английский

A Tunable Cascade Reaction of Ureidomalonates and Alkenyl Azlactones for the Divergent Synthesis of Hydantoins with Distinct Functional Groups DOI
Lin Chen, Di Wang

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

1

Boryl Radical as a Catalyst in Enabling Intra‐ and Intermolecular Cascade Radical Cyclization Reactions: Construction of Polycyclic Molecules DOI
Jie Wang, Yee Lin Phang,

You‐Jie Yu

et al.

Angewandte 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

1

Selective photochemical oxidation of sulfides by Gallium and Sulfur Co-Modified TiO2/g-C3N4 Nanocomposites as catalyst DOI
Razieh Nejat

Journal of Organometallic Chemistry, Journal Year: 2024, Volume and Issue: 1016, P. 123235 - 123235

Published: June 16, 2024

Language: Английский

Citations

1

Metal-free internal nucleophile-triggered domino route for synthesis of fused quinoxaline [1,4]-diazepine hybrids and the evaluation of their DNA binding properties DOI

Bhim Majhi,

Achyut Bora, Subhadeep Palit

et al.

Bioorganic Chemistry, Journal Year: 2024, Volume and Issue: 151, P. 107694 - 107694

Published: Aug. 5, 2024

Language: Английский

Citations

1

Advanced green synthesis: Solvent-free and catalyst-free reaction DOI Creative Commons
Mengyao Li,

Ao Gu,

Jiatong Li

et al.

Green Synthesis and Catalysis, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 1, 2024

Language: Английский

Citations

1