scholarly journals Iminoiodane- and Brønsted Base-Mediated Cross Dehydrogenative Coupling of Cyclic Ethers with 1,3-Dicarbonyl Compounds

Molecules ◽  
2015 ◽  
Vol 20 (7) ◽  
pp. 13336-13353 ◽  
Author(s):  
Ciputra Tejo ◽  
Xiao Sim ◽  
Bo Lee ◽  
Benjamin Ayers ◽  
Chung-Hang Leung ◽  
...  
2019 ◽  
Vol 84 (4) ◽  
pp. 2039-2047 ◽  
Author(s):  
Kishor D. Mane ◽  
Anagh Mukherjee ◽  
Kumar Vanka ◽  
Gurunath Suryavanshi

2019 ◽  
Vol 6 (13) ◽  
pp. 2275-2279 ◽  
Author(s):  
Zhen Zhang ◽  
Yong-Qiang Tu ◽  
Xiao-Ming Zhang ◽  
Fu-Min Zhang ◽  
Shao-Hua Wang

A novel copper-catalyzed highly diastereoselective cross-dehydrogenative coupling reaction for the access of tricyclic chromanes from 8-hydroxyisochromanes and 1,3-dicarbonyl compounds.


ChemInform ◽  
2014 ◽  
Vol 45 (51) ◽  
pp. no-no
Author(s):  
Igor B. Krylov ◽  
Alexander O. Terent'ev ◽  
Vladimir P. Timofeev ◽  
Boris N. Shelimov ◽  
Roman A. Novikov ◽  
...  

2019 ◽  
Vol 43 (19) ◽  
pp. 7403-7408 ◽  
Author(s):  
Kishor D. Mane ◽  
Rohit B. Kamble ◽  
Gurunath Suryavanshi

The white light mediated, 3C alkylation of quinoxalin-2(1H)-ones via a cross dehydrogenative coupling (CDC) reaction with cyclic ethers using eosin Y as a photocatalyst is described. The reaction proceeds via a hydrogen abstraction and transfer process.


2013 ◽  
Vol 15 (17) ◽  
pp. 4600-4603 ◽  
Author(s):  
Zengyang Xie ◽  
Yuping Cai ◽  
Hongwen Hu ◽  
Chen Lin ◽  
Juli Jiang ◽  
...  

2014 ◽  
Vol 356 (10) ◽  
pp. 2266-2280 ◽  
Author(s):  
Igor B. Krylov ◽  
Alexander O. Terent'ev ◽  
Vladimir P. Timofeev ◽  
Boris N. Shelimov ◽  
Roman A. Novikov ◽  
...  

2017 ◽  
Vol 70 (4) ◽  
pp. 430 ◽  
Author(s):  
Ciputra Tejo ◽  
Davin Tirtorahardjo ◽  
David Philip Day ◽  
Dik-Lung Ma ◽  
Chung-Hang Leung ◽  
...  

The synthesis of α,α-diacylaziridines and α,α,β-triacylaziridines from reaction of 2-alkyl-substituted-1,3-dicarbonyl compounds and 2-acyl-substituted-1,4-dicarbonyl compounds with arylsulfonyliminoiodinanes (ArSO2N=IPh) under Brønsted base-mediated atmospheric conditions is described. The reaction mechanism is thought to involve the formal oxidation of the substrate followed by aziridination of the ensuing α,β-unsaturated intermediate by the hypervalent iodine(iii) reagent.


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