ChemInform Abstract: A Convenient Synthetic Route from Isatin N-Mannich Bases to Nitrogen-Containing Derivatives of Isoindigo.

ChemInform ◽  
2011 ◽  
Vol 42 (17) ◽  
pp. no-no
Author(s):  
Andrei V. Bogdanov ◽  
Vladimir F. Mironov ◽  
Lenar I. Musin ◽  
Rashid Z. Musin ◽  
Dmitry B. Krivolapov ◽  
...  
2010 ◽  
Vol 142 (1) ◽  
pp. 81-85 ◽  
Author(s):  
Andrei V. Bogdanov ◽  
Vladimir F. Mironov ◽  
Lenar I. Musin ◽  
Rashid Z. Musin ◽  
Dmitry B. Krivolapov ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 24 (9) ◽  
pp. no-no
Author(s):  
V. N. KOMISSAROV ◽  
V. A. KHARLANOV ◽  
L. YU. UKHIN ◽  
E. YU. BULGAREVICH ◽  
V. I. MINKIN
Keyword(s):  

1994 ◽  
Vol 47 (9) ◽  
pp. 1805 ◽  
Author(s):  
WM Best ◽  
RV Stick ◽  
DMG Tilbrook

The major products in the controlled benzylation (NaH/PhCH2Cl) of allyl and but-3-enyl β-D-glucopyranosides were the 2,4,6-tri-O-benzyl ethers. Subsequent glycosidations of these tribenzyl ethers gave derivatives of allyl and but-3-enyl β- laminaribioside, the latter being subsequently transformed into 3,4-epoxybutyl β- laminaribioside.


2019 ◽  
Vol 15 ◽  
pp. 2524-2533 ◽  
Author(s):  
Shital K Chattopadhyay ◽  
Subhankar Ghosh ◽  
Sarita Sarkar ◽  
Kakali Bhadra

An alternate synthetic route to the important anticancer drug suberoylanilide hydroxamic acid (SAHA) from its α,ß-didehydro derivative is described. The didehydro derivative is obtained through a cross metathesis reaction between a suitable terminal alkene and N-benzyloxyacrylamide. Some of the didehydro derivatives of SAHA were preliminarily evaluated for anticancer activity towards HeLa cells. The administration of the analogues caused a significant decrease in the proliferation of HeLa cells. Furthermore, one of the analogues showed a maximum cytotoxicity with a minimum GI50 value of 2.5 µg/mL and the generation of reactive oxygen species (ROS) as some apoptotic features.


1987 ◽  
Vol 42 (12) ◽  
pp. 1578-1584 ◽  
Author(s):  
Hans Möhrle ◽  
Hubertus Folttmann

AbstractThe aminomethylation of 5-amino-1-naphthol (1) and 5-acetamido-1-naphthol (9) is examined. While the hydrogenolysis of the phenol Mannich bases derived from 1 cannot be accomplished, the derivatives of 9 react easily. The oxidation of the 2-methylphenol compounds 5 and 18 to the corresponding quinones may performed with Fremy's salt. The following transforming of the amino to the hydroxy group by nitrosylsulfuric acid succeeds with small yield only.


2013 ◽  
Vol 9 ◽  
pp. 1517-1525 ◽  
Author(s):  
Marta K Kurpet ◽  
Aleksandra Dąbrowska ◽  
Małgorzata M Jarosz ◽  
Katarzyna Kajewska-Kania ◽  
Nikodem Kuźnik ◽  
...  

A method for the synthesis of N-aryl-C-nitroazoles is presented. A coupling reaction between variously substituted arylboronic acids and 3(5)-nitro-1H-pyrazole catalyzed by copper salt has been carried out in methanol in the presence of sodium hydroxide to afford the desired N-aryl-C-nitroazoles in good yields. This synthetic route has also been successfully applied to obtain N-phenyl derivatives of 4-nitropyrazole, 2-nitroimidazole, 4(5)-nitroimidazole and 3-nitro-1,2,4-triazole.


2018 ◽  
Vol 11 (2) ◽  
pp. 236
Author(s):  
Sushil R. Mathapati ◽  
Vikas B. Suryawanshi ◽  
Abhay S. Bondge ◽  
Jairaj K. Dawale
Keyword(s):  

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