Loading…

Thermo-/photo-catalysts for aerobic oxidative cyanation of diverse oxygen-containing feedstocks

Nitriles constitute essential components in a vast array of both bulk and fine chemicals, as well as in various bioactive molecules. The aerobic oxidative cyanation of diverse oxygen-containing feedstocks, including alcohols, aldehydes, and ketones, stands out as a green and highly promising avenue...

Full description

Saved in:
Bibliographic Details
Published in:Green chemistry : an international journal and green chemistry resource : GC 2024-02, Vol.26 (4), p.1831-1845
Main Authors: He, Jie, Zhou, Peng, Zhang, Shiying, Lam, Jason Chun-Ho, Liao, Yuhe, Zhang, Zehui
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Nitriles constitute essential components in a vast array of both bulk and fine chemicals, as well as in various bioactive molecules. The aerobic oxidative cyanation of diverse oxygen-containing feedstocks, including alcohols, aldehydes, and ketones, stands out as a green and highly promising avenue for nitrile synthesis over both thermocatalysts and photocatalysts. In this review, we initially elucidate the reaction mechanisms involved in the oxidative cyanation of oxygen-containing compounds. Following this, we present a summary and commentary on the predominantly achieved progress in the oxidative cyanation of various oxygen-containing feedstocks over the last decade. The categorization is based on types of catalysts, including non-noble metal catalysts, single-metal-atom catalysts, metal-free catalysts, and photocatalysts. Additionally, we assess the current catalytic systems from the standpoint of green chemistry. Finally, we conclude by highlighting the current challenges and delineating our prospects for future research endeavors. Aerobic oxidative cyanation of diverse oxygen-containing compounds over thermo- and photocatalysts is highlighted as a green and promising avenue for nitrile synthesis.
ISSN:1463-9262
1463-9270
DOI:10.1039/d3gc04548j