scholarly journals One-pot synthesis of polysubstituted indoles from aliphatic nitro compounds under mild conditions

2007 ◽  
Vol 48 (10) ◽  
pp. 1809-1811 ◽  
Author(s):  
Christopher A. Simoneau ◽  
Alexis M. Strohl ◽  
Bruce Ganem
ChemInform ◽  
2007 ◽  
Vol 38 (25) ◽  
Author(s):  
Christopher A. Simoneau ◽  
Alexis M. Strohl ◽  
Bruce Ganem

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.


2015 ◽  
Vol 33 (4) ◽  
pp. 401-404 ◽  
Author(s):  
Wei Zhang ◽  
Yanjing Wang ◽  
Cuibing Bai ◽  
Jialong Wen ◽  
Naixing Wang

ChemInform ◽  
2015 ◽  
Vol 46 (33) ◽  
pp. no-no
Author(s):  
Wei Zhang ◽  
Yanjing Wang ◽  
Cuibing Bai ◽  
Jialong Wen ◽  
Naixing Wang

Synthesis ◽  
2019 ◽  
Vol 51 (22) ◽  
pp. 4215-4230 ◽  
Author(s):  
Adesh Kumar Singh ◽  
Rapelly Venkatesh ◽  
Jeyakumar Kandasamy

The palladium-catalyzed one-pot synthesis of 2,3-deoxy-3-keto aryl C-glycosides is achieved from glycals and anilines in the presence of tert-butyl nitrite and aqueous HBF4 under mild conditions. This one-pot method stereospecifically provides α- and β-aryl glycosides (≥19:1 by NMR) in good yields at room temperature. The configuration at the C-3 position in the glycal determines the anomeric selectivity (i.e., α or β) of the desired products.


2020 ◽  
Vol 39 (5-6) ◽  
pp. 267-287
Author(s):  
Shuang Hao ◽  
Shuai Lin ◽  
Xin Wang ◽  
Ran An ◽  
Mengbi Guo ◽  
...  

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