Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Bang-Yi Wei"'
Autor:
Dong‐Tai Xie, Hong‐Lei Chen, Dian Wei, Bang‐Yi Wei, Zheng‐Hu Li, Jian‐Wu Zhang, Wei Yu, Bing Han
Publikováno v:
Angewandte Chemie International Edition. 61
A novel distal radical rearrangement of alkoxyphosphine is developed for the first time and applied to the regioselective radical fluoroalkylphosphorylation of unactivated olefins. By employing a one-pot two-step reaction of (bis)homoallylic alcohols
Publikováno v:
Angewandte Chemie. 133:3219-3225
This work represents the first [4+2] annulation of hydroxamic acids with olefins for the synthesis of benzo[c][1,2]oxazines scaffold via anode-selective electrochemical oxidation. This protocol features mild conditions, is oxidant free, shows high re
Autor:
Dong-Tai Xie, Hong-Lei Chen, Dian Wei, Bang-Yi Wei, Zheng-Hu Li, Jian-Wu Zhang, Wei Yu, Bing Han
A regioselective radical fluoroalkylphosphorylation of unactivated alkenes has been developed by a one-pot twosteps reaction of (bis)homoallylic alcohols, organophosphine chlorides (R2PCl), and fluoroalkyl iodides (RFI) under visible light irradiatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bb2240f71d1f214c345d776e444a9f7
https://doi.org/10.26434/chemrxiv-2022-vnh52
https://doi.org/10.26434/chemrxiv-2022-vnh52
Autor:
Bang-Yi Wei, Dian Wei, Jian-Wu Zhang, Tuming Liu, Ning Jiao, Yi-Heng He, Bing Han, Jiahao Pan
Publikováno v:
Angewandte Chemie (International ed. in English). 60(50)
A novel radical 1,4/5-amino shift from the oxygen center of alkene-tethered diphenyl ketoxime ethers to the carbon center to achieve high value-added fluoroalkyl-containing primary β(γ)-amino-ketones is reported. Mechanism studies reveal that the m
Publikováno v:
Angewandte Chemie (International ed. in English). 60(40)
A tunable photocatalytic method is reported for anti-Markovnikov hydro- and aminooxygenation of unactivated alkenes using readily accessible ketoxime carbonates as the diverse functionalization reagents. Mechanistic studies reveal that this reaction
Publikováno v:
ACS Catalysis. 9:4179-4188
A 4-HO-TEMPO-catalyzed redox strategy for the synthesis of pyridines through the annulation of cyclopropanols and oxime acetates has been developed. This protocol features good functional group tol...
Autor:
Yi-Heng He, Bang-Yi Wei, Tuming Liu, Ning Jiao, Bing Han, Jiahao Pan, Jian-Wu Zhang, Dian Wei
Publikováno v:
Angewandte Chemie International Edition. 60:26020-26020
Publikováno v:
Organic letters. 20(14)
A copper-catalyzed aminoacyloxylation of unactivated alkenes of unsaturated hydrazones is achieved by using various commercially available carboxylic acids as the acyloxylating reagents and di- tert-butyl peroxide (DTBP) as the oxidant. By using this