scholarly journals Erratum: Aldol Condensation and Michael Addition of 4,4-Dimethylcyclohexane-1,3-dione and Aromatic Aldehydes. Unconventional Substituent Effects

2012 ◽  
Vol 30 (1) ◽  
pp. 204-204
Author(s):  
Muharrem Kaya
RSC Advances ◽  
2019 ◽  
Vol 9 (48) ◽  
pp. 27883-27887
Author(s):  
Xiao-Mu Hu ◽  
Hai Dong ◽  
Yue-Dan Li ◽  
Ping Huang ◽  
Zhuang Tian ◽  
...  

3,4,5-Trisubstituted isoxazoles were prepared, using a tandem grinding strategy, from aromatic aldehydes, 3,5-dimethyl-4-nitroisoxazole and activated methylene compounds in the presence of pyrrolidine and Et3N with high yields and efficiency.


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.


RSC Advances ◽  
2014 ◽  
Vol 4 (100) ◽  
pp. 57016-57025 ◽  
Author(s):  
Eethamukkala Ubba ◽  
Fazlur-Rahman Nawaz Khan ◽  
Euh Duck Jeong ◽  
Eun Hyuk Chung

Microwave supported, water intervened, nano crystalline TiO2 catalyzed synthesis of 3-(1,5-dioxo-1,5-diphenylpentan-3-yl)quinolin-2(1H)-ones, is described.


Author(s):  
Fengan Han ◽  
Jingyuan Xu ◽  
Guangyi Li ◽  
Jilei Xu ◽  
Aiqin Wang ◽  
...  

High-density and low freezing point dicycloalkanes were synthesized by the aldol condensation of methyl isobutyl ketone with aromatic aldehydes followed by hydrodeoxygenation under solvent-free conditions.


ChemInform ◽  
2005 ◽  
Vol 36 (3) ◽  
Author(s):  
S. Z. Vatsadze ◽  
V. N. Nuriev ◽  
I. F. Leshcheva ◽  
N. V. Zyk

1963 ◽  
Vol 41 (4) ◽  
pp. 817-820 ◽  
Author(s):  
Frances C. Brown ◽  
R. Sidney Jones ◽  
Mildred Kent

The aldol condensation between 2,3-diphenyl-4-thiazolidinone and aromatic aldehydes, which cannot be effected by the usual catalysts used in the analogous reactions of 2-thiono-, 2-oxo-, and 2-imino-4-thiazolidinones, was achieved by the use of ethoxide ion. The structure of the 2,3-diphenyl-5-arylidene-4-thiazolidinone was confirmed by ultraviolet spectral data.


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