Phthalimidine Synthesis via Iridium-Catalyzed Reductive Lactamization DOI
Jingyu Zhang, Chen Yang, Jiaxi Xu

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 24, 2024

Herein, we report a sustainable and efficient method for the synthesis of structurally diverse phthalimidines from 2-formylbenzoic acid primary amines using an iridium-catalyzed reductive lactamization strategy. The advantages this method, such as use water–ethanol solvent, broad substrate scope, high catalyst efficiency (S/C up to 10000), good scalability, easy purification, enable it be practical approach phthalimidines. It is suggested that iridium hydride formation involved in rate-limiting step. Synthetic applications late-stage functionalization medicinally relevant molecules are also demonstrated.

Language: Английский

En Route to Diastereopure Polycyclic γ‐Lactones by Iridium‐Catalyzed Hydride Transfer DOI Open Access
Yang Chen, Jingyu Zhang, Yecheng Wang

et al.

Chinese Journal of Chemistry, Journal Year: 2024, Volume and Issue: 42(23), P. 3047 - 3055

Published: July 30, 2024

Comprehensive Summary The reductive lactonization strategy provides an efficient access to diastereoenriched polycyclic γ‐lactones. However, it is still a formidable challenge develop and versatile protocol with excellent levels of diastereocontrol. Herein, we provide highly diastereoselective route diastereopure bi‐ γ‐lactones, by means iridium‐catalyzed hydride transfer strategy. This method features high diastereocontrol, broad substrate scope, catalyst efficiency ( S / C = up 5000). Mechanistic studies suggest that the iridium formation might be rate‐determining step, step diastereo‐determining step. large steric hindrance species intramolecular hydrogen bonding are critically key diastereocontrol process. From perspectives configurational analysis Duniz angles attack, nature well rationalized. A more general empirical rule based on facial selectivity for explaining predicting stereochemistry also proposed.

Language: Английский

Citations

2

Iridium-Catalyzed Highly Selective 1,4-Reduction of α,β-Unsaturated Carbonyl Compounds DOI Creative Commons
You-Wei Chen, Jide Li, Jiaxi Xu

et al.

Molecules, Journal Year: 2024, Volume and Issue: 29(24), P. 5912 - 5912

Published: Dec. 14, 2024

In this study, an iridium-catalyzed selective 1,4-reduction of α,β-unsaturated carbonyl compounds is realized, with water as a solvent and formic acid hydride donor. The new efficient iridium catalyst features 2-(4,5-dihydroimidazol-2-yl)quinoline ligand. chemoselectivity efficiency are highly dependent on the electronic steric properties substrates. For amides, acids, esters, only electron-deficient C=C bonds reduced (1,4-reduction), other functional groups left intact. S/C ratio initial TOF reach 7000 18,480 h−1, respectively. A gram-scale also performed. Deuterium labeling shows that β-hydrogens products originate from formyl hydrogen in acid. application for modification structures some medications demonstrated.

Language: Английский

Citations

0

Phthalimidine Synthesis via Iridium-Catalyzed Reductive Lactamization DOI
Jingyu Zhang, Chen Yang, Jiaxi Xu

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 24, 2024

Herein, we report a sustainable and efficient method for the synthesis of structurally diverse phthalimidines from 2-formylbenzoic acid primary amines using an iridium-catalyzed reductive lactamization strategy. The advantages this method, such as use water–ethanol solvent, broad substrate scope, high catalyst efficiency (S/C up to 10000), good scalability, easy purification, enable it be practical approach phthalimidines. It is suggested that iridium hydride formation involved in rate-limiting step. Synthetic applications late-stage functionalization medicinally relevant molecules are also demonstrated.

Language: Английский

Citations

0