ChemInform Abstract: A Predominately anti-Stereoselective Chiral Metal-Directed Aldol Condensation with Aromatic Aldehydes.

ChemInform ◽  
1990 ◽  
Vol 21 (20) ◽  
Author(s):  
L. N. PRIDGEN ◽  
A. MAGID ◽  
I. LANTOS
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.


2014 ◽  
Vol 44 (9) ◽  
pp. 1245-1250 ◽  
Author(s):  
Val V. Martichonok ◽  
Peter K. Chiang ◽  
Padraick J. Dornbush ◽  
Kirkwood M. Land

2011 ◽  
Vol 8 (2) ◽  
pp. 863-869 ◽  
Author(s):  
Tapas K. Mandal ◽  
Rammohan Pal ◽  
Rina Mondal ◽  
Asok K. Mallik

Different aromatic aldehydes and cinnamaldehyde undergo cross-aldol condensation with chroman-4-ones and1-thiochroman-4-ones in the presence of amberlyst-15 under microwave irradiation in solvent free condition to afford rapidly the correspondingE-3-arylidene andE-3-cinnamylidene derivatives, respectively, in high yield. This process is simple, efficient and environmentally benign.


ChemInform ◽  
2003 ◽  
Vol 34 (8) ◽  
Author(s):  
Peyman Salehi ◽  
Mohammad M. Khodaei ◽  
Mohammad A. Zolfigol ◽  
Afsaneh Keyvan

2009 ◽  
Vol 39 (2) ◽  
pp. 201-207 ◽  
Author(s):  
Dailei Song ◽  
Yongli Chen ◽  
Runxia Wang ◽  
Chunsheng Liu ◽  
Heng Jiang ◽  
...  

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