دورية أكاديمية

Photoredox-Enabled Chromium-Catalyzed Alkene Diacylations

التفاصيل البيبلوغرافية
العنوان: Photoredox-Enabled Chromium-Catalyzed Alkene Diacylations
المؤلفون: Jing Liu (38537), Liang-Qiu Lu (1546135), Yixin Luo (712865), Wei Zhao (14321), Peng-Chao Sun (11978018), Weiwei Jin (263276), Xiaotian Qi (1425286), Ying Cheng (288456), Wen-Jing Xiao (1528693)
سنة النشر: 2022
المجموعة: Smithsonian Institution: Digital Repository
مصطلحات موضوعية: Biochemistry, Microbiology, Genetics, Biotechnology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, widely used palladium, modern synthetic chemistry, dual catalysis system, catalyzed radical diacylation, light photoredox catalysis, 4 -, synthetic utility, nickel catalysis, chromium catalysis, catalyzed cross, 6 -, vinyl cyclopropanes, valuable 1, successfully applied, proposed according, powerful tool, possible mechanism, mild conditions, giving access, flexible chromium, enabled chromium, diverse heterocycles, dft calculations
الوقت: 1
الوصف: Transition-metal-catalyzed cross-coupling reactions are a powerful tool to construct carbon–carbon bonds in modern synthetic chemistry. Chromium catalysis is much less developed compared with the widely used palladium and nickel catalysis. Herein, we reported an efficient and flexible chromium-catalyzed radical diacylation of alkenes with the help of visible-light photoredox catalysis, giving access to valuable 1,4-, 1,6-, and 1,7-diones under mild conditions. The synthetic utility of this methodology was proven by converting diones to diverse heterocycles. Furthermore, the same dual catalysis system can be successfully applied to dienes and vinyl cyclopropanes. A possible mechanism of alkene diacylation via dual photoredox/chromium catalysis was proposed according to control experiments and DFT calculations.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
العلاقة: https://figshare.com/articles/journal_contribution/Photoredox-Enabled_Chromium-Catalyzed_Alkene_Diacylations/18780023Test
DOI: 10.1021/acscatal.1c05672.s001
الإتاحة: https://doi.org/10.1021/acscatal.1c05672.s001Test
حقوق: CC BY-NC 4.0
رقم الانضمام: edsbas.19B58460
قاعدة البيانات: BASE