| Literature DB >> 33797933 |
Hua Wang1, Jian-Ping Qu2, Yan-Biao Kang1.
Abstract
A recyclable organic photoreductant (1 mol % CBZ6)-catalyzed reductive (pinacol) coupling of aldehydes, ketones, and imines has been developed. Irradiated by purple light (407 nm) using triethylamine as an electron donor, a variety of 1,2-diols and 1,2-diamines could be prepared. The oxidation potential of the excited state of CBZ6 is established as -1.92 V (vs saturated calomel electrode (SCE)). The relative high reductive potential enables the reductive coupling of carbonyl compounds and their derivatives. CBZ6 can be prepared in gram scale and is acid/base- or air-stable. It could be applied in large-scale photoreductive synthesis and recovered in high yield after the reaction.Entities:
Year: 2021 PMID: 33797933 DOI: 10.1021/acs.orglett.1c00537
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005