Active Functional Group-coated VO2(B) Nanorods: Facile One-pot Hydrothermal Synthesis and Conversion to V2O3

2014 ◽  
Vol 43 (3) ◽  
pp. 337-339 ◽  
Author(s):  
Yifu Zhang ◽  
Xiongzhi Zhang ◽  
Yu Huang ◽  
Mei Xiao ◽  
Fei Niu ◽  
...  
2020 ◽  
Author(s):  
José Tiago Menezes Correia ◽  
Gustavo Piva da Silva ◽  
Camila Menezes Kisukuri ◽  
Elias André ◽  
Bruno Pires ◽  
...  

A metal- and catalyst-free photoinduced radical cascade hydroalkylation of 1,7-enynes has been disclosed. The process is triggered by a SET event involving a photoexcited electron-donor-aceptor complex between NHPI ester and Hantzsch ester, which decomposes to afford a tertiary radical that is readily trapped by the enyne. <a>The method provides an operationally simple, robust and step-economical approach to the construction of diversely functionalized dihydroquinolinones bearing quaternary-centers. A sequential one-pot hydroalkylation-isomerization approach is also allowed giving access to a family of quinolinones. A wide substrate scope and high functional group tolerance was observed in both approaches</a>.


2021 ◽  
Vol 46 (27) ◽  
pp. 13946-13951
Author(s):  
P.C. Nagajyothi ◽  
R. Ramaraghavulu ◽  
K. Munirathnam ◽  
K. Yoo ◽  
Jaesool Shim

2011 ◽  
Vol 21 (21) ◽  
pp. 7795 ◽  
Author(s):  
Jianfeng Shen ◽  
Min Shi ◽  
Bo Yan ◽  
Hongwei Ma ◽  
Na Li ◽  
...  

2012 ◽  
Vol 18 (15) ◽  
pp. 4681-4686 ◽  
Author(s):  
Peng Gao ◽  
Longqiang Wang ◽  
Ying Wang ◽  
Yujin Chen ◽  
Xiaona Wang ◽  
...  

Synthesis ◽  
2021 ◽  
Author(s):  
Santanu Ghora ◽  
Chinnabattigalla Sreenivasulu ◽  
Gedu Satyanarayana

AbstractAn efficient, one-pot, domino synthesis of quinolines via the coupling of iodoanilines with allylic alcohols facilitated by palladium catalysis is described. The overall synthetic process involves an intermolecular Heck coupling between 2-iodoanilines and allylic alcohols, intramolecular condensation of in situ generated ketones with an internal amine functional group, and a dehydrogenation sequence. Notably, this protocol occurs in water as a green solvent. Significantly, the method exhibits broad substrate scope and is applied for the synthesis of deuterated quinolines through a deuterium-exchange process.


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