ChemInform Abstract: Catalyst Free Michael Addition of 3-Methyl-2-pyrazolin-5-one to β-Nitrostyrenes “on Water”: A Green Protocol for Facile Synthesis of 4-(1-Aryl-2-nitroethyl)-3-methyl-1H-pyrazol-5-ol.

ChemInform ◽  
2014 ◽  
Vol 45 (10) ◽  
pp. no-no
Author(s):  
H. M. Meshram ◽  
Nadigama Satish Kumar ◽  
Jagadeesh Babu Nanubolu ◽  
L. Chandrasekhara Rao ◽  
N. Nageswara Rao
2013 ◽  
Vol 54 (45) ◽  
pp. 5941-5944 ◽  
Author(s):  
H.M. Meshram ◽  
Nandigama Satish Kumar ◽  
Jagadeesh Babu Nanubolu ◽  
L. Chandrasekhara Rao ◽  
N. Nageswara Rao

2014 ◽  
Vol 12 (14) ◽  
pp. 2185-2188 ◽  
Author(s):  
Zhuzhou Shao ◽  
Lubin Xu ◽  
Liang Wang ◽  
Hongtao Wei ◽  
Jian Xiao

The tandem Michael addition/decarboxylation of (thio)-coumarin-3-carboxylic acids with indoles gives biologically important indole-3-substituted dihydrocoumarins in good to excellent yields under catalyst-free conditions.


Synlett ◽  
2018 ◽  
Vol 29 (12) ◽  
pp. 1589-1592 ◽  
Author(s):  
Abolfazl Olyaei ◽  
Mahnaz Saraei ◽  
Reyhaneh Khoeiniha

A high-yielding cyclocondensation of 4-hydroxycoumarin, phenylglyoxal monohydrate, and heteroarylamines proceeds without catalysis, which gives novel functionalized furo[3,2-c]coumarins and heteroarylamino alkylation of coumarin products in acetonitrile under reflux, is reported for the first time. This tandem process involves sequentially an aldol condensation, Michael addition, a ring closure, and dehydration reaction.


2014 ◽  
Vol 38 (11) ◽  
pp. 5536-5543 ◽  
Author(s):  
Hamid Khanmohammadi ◽  
Khatereh Rezaeian

Novel imidazo[4,5-f][1,10]phenanthroline ligand and its corresponding Ru(ii) complex are synthesized from green protocol for colorimetric detection of anions in water.


Tetrahedron ◽  
2019 ◽  
Vol 75 (51) ◽  
pp. 130761 ◽  
Author(s):  
Divya K. Nair ◽  
Sudheesh T. Sivanandan ◽  
Pravin Kendrekar ◽  
Irishi N.N. Namboothiri

Synlett ◽  
2017 ◽  
Vol 28 (15) ◽  
pp. 1994-1999
Author(s):  
Santhosh Chittimalla ◽  
Chennakesavulu Bandi ◽  
Vinod Gadi ◽  
Siva Gunturu

3-Alkylindoles on reaction with a cyclohexa-2,4-dien-1-one catalyzed by BF3·OEt2 gave the corresponding 3-alkyl-3-arylindolenines in high yields through a tandem Michael addition/aromatization sequence. In the presence of HCl, these indolenine derivatives underwent a facile Plancher-type C-3 to C-2 aryl rearrangement to deliver the corresponding 2-arylindoles.


Heterocycles ◽  
2013 ◽  
Vol 87 (10) ◽  
pp. 2023 ◽  
Author(s):  
Jason Guy Taylor ◽  
Wellington Martins Ventura ◽  
Luiz Guilherme Souza de Assis

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