Electronic effect of substituents on anilines favors 1,4-addition totrans-β-nitrostyrenes: access toN-substituted 3-arylindoles and 3-arylindoles

2018 ◽  
Vol 16 (20) ◽  
pp. 3760-3770 ◽  
Author(s):  
Radhakrishna Gattu ◽  
Suchandra Bhattacharjee ◽  
Karuna Mahato ◽  
Abu T. Khan

A simple and an efficient method for the regioselective synthesis ofN-alkyl/aryl/H 3-arylindole derivatives fromN-substituted anilines andtrans-β-nitrostyrenes has been described using 10 mol% of bismuth(iii) triflate as a catalyst in acetonitrile at 80 °C.

1979 ◽  
Vol 44 (3) ◽  
pp. 750-755 ◽  
Author(s):  
Josef Pola ◽  
Marie Jakoubková ◽  
Václav Chvalovský

Relative basicity of the oxygen in alkoxysilanes (RO)nSi(CH3)3-n having n = 1-4 and various electrondonating and electronwithdrawing groups R measured as Δν(OH) of phenol due to its interaction with these compounds in CCl4 is shown to be chiefly controlled by the electronic effect of substituents R. Linear regression analysis of the Δν(OH) vs n relatioship for individual series (RO)nSi(CH3)4-n suggests the operation of the polarizability effect of RO groups becoming more important with increasing electronwithdrawing nature of R.


ChemInform ◽  
2011 ◽  
Vol 42 (29) ◽  
pp. no-no
Author(s):  
Helio G. Bonacorso ◽  
Cleber A. Cechinel ◽  
Jussara Navarini ◽  
Rosalia Andrighetto ◽  
Marcos A. P. Martins ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 30 (24) ◽  
pp. no-no
Author(s):  
Thomas F. Woiwode ◽  
Christoph Rose ◽  
Thomas J. Wandless

2016 ◽  
Vol 86 (4) ◽  
pp. 806-809 ◽  
Author(s):  
M. V. Il’in ◽  
D. S. Bolotin ◽  
M. Ya. Demakova ◽  
M. S. Avdontseva

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