Asymmetric Synthesis of Isoindolin-1-ones from Enamides via Pd-Catalyzed Intramolecular Reductive Heck Reaction DOI
М. А. Ashatkina,

D.I. Shamshina,

Vadim A. Shiryaev

и другие.

Russian Journal of General Chemistry, Год журнала: 2025, Номер 95(1), С. 30 - 34

Опубликована: Янв. 1, 2025

Язык: Английский

Recent Advances on Asymmetric Synthesis of Dihydroflavones DOI Creative Commons

Zhihao Du,

Guojing Li,

Wenhao Dai

и другие.

Pharmaceutical Fronts, Год журнала: 2025, Номер unknown

Опубликована: Фев. 28, 2025

Dihydroflavones, as an important part of flavonoid compounds, possess a wide range physiological activities and significant medicinal values. The importance these compounds has driven the research on preparation dihydroflavonoid many chiral can be obtained with potential activity, excellent yields, stereoselectivity using various effective synthetic strategies. This paper reviews biological single-configuration flavanones provides comprehensive overview progress in asymmetric synthesis this group flavonoids from 2002 to 2024, including (1) ortho-hydroxy chalcones, (2) chromones, (3) reduction, (4) intramolecular Mitsunobu carbene insertion. These methods provide some efficient economical strategies for flavanones, especially enantioenriched aspects.

Язык: Английский

Процитировано

0

Asymmetric Synthesis of Isoindolin-1-ones from Enamides via Pd-Catalyzed Intramolecular Reductive Heck Reaction DOI
М. А. Ashatkina,

D.I. Shamshina,

Vadim A. Shiryaev

и другие.

Russian Journal of General Chemistry, Год журнала: 2025, Номер 95(1), С. 30 - 34

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0