Photoredox-mediated cobalt catalysis for non-asymmetric and asymmetric synthesis DOI Creative Commons

Zhiyong Chi,

Yuhang He,

Ablimit Abdukader

и другие.

Cell Reports Physical Science, Год журнала: 2025, Номер unknown, С. 102613 - 102613

Опубликована: Май 1, 2025

Язык: Английский

Chiral ruthenium complex/Ph 2 P(2-furyl)–catalyzed asymmetric nucleophilic addition of aryl aldehyde hydrazones to simple ketones DOI Creative Commons

Chenghao Zhu,

Zihao Ye, Haining Wang

и другие.

Science Advances, Год журнала: 2025, Номер 11(12)

Опубликована: Март 21, 2025

An efficient synthesis of chiral tertiary alcohols through asymmetric nucleophilic addition reaction aldehyde hydrazones to simple ketones (especially aryl/methyl ketones) has been well established. Aryl aldehydes could be used as latent benzyl carbanion equivalents via reductive polarity reversal. The key the success was combination an achiral monophosphine ligand Ph 2 P(2-furyl) with a diamine derivative, which enhanced enantioselectivity and reactivity. Density functional theory calculations revealed hydrogen bond interactions between ligand, base anion, combined induce desired enantioselectivity. Moreover, further synthetic transformation high chirality transfer also demonstrated.

Язык: Английский

Процитировано

0

Benzothiazolines Acting as Carbanion and Radical Transfer Reagents in Carbon–Carbon Bond Construction DOI Creative Commons
Xiaotang Chen,

Bao‐Chen Qian

Molecules, Год журнала: 2025, Номер 30(8), С. 1711 - 1711

Опубликована: Апрель 11, 2025

Traditionally employed as hydrogenation reagents, benzothiazolines have emerged versatile carbanion and radical transfer playing a vital role in the construction of various carbon-carbon bonds. The cutting-edge progress photochemistry chemistry prompted study visible light-driven reactions, bringing into vibrant focus. Their chemical processes been uncovered to encompass variety activation mechanisms, with five distinct modes having identified. This work reviews innovative applications donors alkyl or acyl groups, achieving hydroalkylation hydroacylation substitution. By examining their diverse this review highlights potential serving groups for further research development. Moreover, will offer exemplary inspiration synthetic chemists, contributing ongoing evolution utility organic synthesis.

Язык: Английский

Процитировано

0

Photoredox-mediated cobalt catalysis for non-asymmetric and asymmetric synthesis DOI Creative Commons

Zhiyong Chi,

Yuhang He,

Ablimit Abdukader

и другие.

Cell Reports Physical Science, Год журнала: 2025, Номер unknown, С. 102613 - 102613

Опубликована: Май 1, 2025

Язык: Английский

Процитировано

0