New Quinoline Derivatives on the Basis of 4-(Hydroxy-2-methylquinolin-3-yl)acetic Acid.

ChemInform ◽  
2005 ◽  
Vol 36 (8) ◽  
Author(s):  
A. A. Avetisyan ◽  
I. L. Aleksanyan ◽  
A. A. Pivazyan
Synthesis ◽  
2017 ◽  
Vol 50 (06) ◽  
pp. 1350-1358 ◽  
Author(s):  
Cunde Wang ◽  
Xushun Qing ◽  
Ting Wang ◽  
Chenlu Dai ◽  
Zhenjie Su

An efficient iron/acetic acid system-mediated reductive cyclization reaction of substituted 2-aryl-3-nitro-2H-chromenes with substituted 2-nitrobenzaldehydes for the synthesis of 6-aryl-6H-chromeno[3,4-b]quinolines was developed. This reaction involves the sequential reduction, hydrolysis, aldol condensation, intramolecular addition, and the nucleophilic addition of substituted 2-aryl-3-nitro-2H-chromenes with substituted 2-nitrobenzaldehydes to give the corresponding 6H-chromeno[3,4-b]quinolines. This transformation provides a straightforward synthetic protocol for constructing substituted 6H-chromeno[3,4-b]quinoline derivatives. The structures of three typical products were confirmed by X-ray crystallography.


2010 ◽  
Vol 51 (40) ◽  
pp. 5234-5237 ◽  
Author(s):  
Chintakunta Ramesh ◽  
Veerababurao Kavala ◽  
Chun-Wei Kuo ◽  
Ching-Fa Yao

ChemInform ◽  
2010 ◽  
Vol 42 (3) ◽  
pp. no-no
Author(s):  
Chintakunta Ramesh ◽  
Veerababurao Kavala ◽  
Chun-Wei Kuo ◽  
Ching-Fa Yao

1984 ◽  
Vol 49 (11) ◽  
pp. 2628-2634 ◽  
Author(s):  
Jan Slouka ◽  
Vojtěch Bekárek ◽  
Karel Nálepa ◽  
Antonín Lyčka

o-Nitrophenylpyruvic acid thiosemicarbazone (I) has been cyclized to 2-thio-5-(o-nitrobenzyl)-6-azauracil (II) which has been transformed in 5-(o-nitrobenzyl)-6-azauracil (III) by both oxidation, and methylation and hydrolysis of the 3-methylmercapto-6-(o-nitrobenzyl)-2,5-dihydro-1,2,4-triazin-5-one (V) formed. Reduction of derivative III with iron(II) hydroxide and cyclization of the amino derivative IV formed gives 2,3,4,10-tetrahydro-1,2,4-triazino[5,6-b]quinolin-3-one (VI). Compound VI is transformed in acid medium to 1-amino-1,2-dihydroimidazo[4,5-b]quinolin-2-one (VIII) via the tautomer VII, and in boiling acetic acid it gives the acetylamino derivative IX. The N-amino derivative VIII reacts with carbonyl compounds to give the corresponding hydrazones X - XII, and its nitrosation gives 1,2-dihydroimidazo[4,5-b]quinolin-2-one (XIII).


2004 ◽  
Vol 40 (6) ◽  
pp. 889-891 ◽  
Author(s):  
A. A. Avetisyan ◽  
I. L. Aleksanyan ◽  
A. A. Pivazyan

ChemInform ◽  
2015 ◽  
Vol 46 (11) ◽  
pp. no-no
Author(s):  
R. R. Rajawinslin ◽  
Sachin D. Gawande ◽  
Veerababurao Kavala ◽  
Yi-Hsiang Huang ◽  
Chun-Wei Kuo ◽  
...  

RSC Advances ◽  
2014 ◽  
Vol 4 (71) ◽  
pp. 37806-37811 ◽  
Author(s):  
R. R. Rajawinslin ◽  
Sachin D. Gawande ◽  
Veerababurao Kavala ◽  
Yi-Hsiang Huang ◽  
Chun-Wei Kuo ◽  
...  

An efficient iron/acetic acid mediated one pot reductive cyclization protocol was successfully developed for the synthesis of acridinone and quinoline derivatives.


Author(s):  
N.C. Lyon ◽  
W. C. Mueller

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.


2001 ◽  
Vol 120 (5) ◽  
pp. A153-A153
Author(s):  
S MIYAMOTO ◽  
K KATO ◽  
Y ISHII ◽  
S ASAI ◽  
T NAGAISHI ◽  
...  

2004 ◽  
Vol 171 (4S) ◽  
pp. 94-94
Author(s):  
Yao-Chi Chuang ◽  
Naoki Yoshimura ◽  
Chao-Cheng Huang ◽  
Po-Hui Chiang ◽  
Michael B. Chancellor

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