aliphatic nitro compounds
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2020 ◽  
Vol MA2020-01 (45) ◽  
pp. 2565-2565
Author(s):  
Nicolas Holubowitch ◽  
Zachary Budimir ◽  
Cameo Crabtree

2020 ◽  
Vol 33 (1) ◽  
pp. 49-52
Author(s):  
Nitin Srivastava ◽  
B.K. Rathore ◽  
R.K. Vishnoi ◽  
Sangeeta Bajpai

A simple way of synthesis of artemisinin dimer using nitro aliphatic compounds is reported. Herein, few artemisinin monomers and dimers have been synthesized with the help of linker nitroalkanes using iron catalyst supported on polymer (Fe/SBA-15). The synthesized artemisinin shows good anticancer and antimalarial activities


2019 ◽  
Vol 55 (6) ◽  
pp. 541-546 ◽  
Author(s):  
Nicolai A. Aksenov ◽  
Anton A. Skomorokhov ◽  
Alexander V. Aksenov ◽  
Leonid G. Voskressensky ◽  
Michael A. Rubin

2019 ◽  
Vol 58 (20) ◽  
pp. 6713-6717 ◽  
Author(s):  
Marian Rauser ◽  
Raphael Eckert ◽  
Max Gerbershagen ◽  
Meike Niggemann

2019 ◽  
Vol 131 (20) ◽  
pp. 6785-6789 ◽  
Author(s):  
Marian Rauser ◽  
Raphael Eckert ◽  
Max Gerbershagen ◽  
Meike Niggemann

Synlett ◽  
2019 ◽  
Vol 30 (05) ◽  
pp. 615-619 ◽  
Author(s):  
Ji-Yu Wang ◽  
Xu-Ling Chen ◽  
Yu Dong ◽  
Shuai He ◽  
Rui Zhang ◽  
...  

A one-pot synthesis of 2-(N-substituted amino)-1,4-naphthoquinones from 1,4-naphthoquinones and nitro compounds in water has been developed. This method features mild reaction conditions and provides aromatic nitro compounds with various functional groups such as halogens, methylthio, ester, amide, even allyl, propargyl, and heterocycles, as well as aliphatic nitro compounds that are well tolerated. This method can be scaled up and we conducted further transformation of the obtained 2-(N-substituted amino)-1,4-naphthoquinones to synthesize carbazolequinone derivatives.


2019 ◽  
Vol 17 (24) ◽  
pp. 5997-6006 ◽  
Author(s):  
Yulia A. Antonova ◽  
Yulia V. Nelyubina ◽  
Alexey Yu. Sukhorukov ◽  
Sema L. Ioffe ◽  
Andrey A. Tabolin

A novel efficient regioselective method for the carbon chain activation of aliphatic nitro compounds is described using a tandem double acylation/[3,3]-rearrangement sequence.


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