scholarly journals A CONVENIENT METHOD FOR THE PREPARATION OF CARBOXYLIC ACID FLUORIDES

1976 ◽  
Vol 5 (4) ◽  
pp. 303-306 ◽  
Author(s):  
Teruaki Mukaiyama ◽  
Toshio Tanaka
1950 ◽  
Vol 28b (9) ◽  
pp. 556-560 ◽  
Author(s):  
F. A. Vandenheuvel ◽  
P. Yates

The Arndt–Eistert reaction offers a convenient method for the synthesis of the higher members of the aliphatic carboxylic acid series. Nonadecanoic acid, eicosanoic acid, and heneicosanoic acid have been prepared successively from stearic acid in good yields. An efficient method of purification of the synthetic products is described. The ultraviolet absorption maxima for some diazoketones derived from the higher members of the aliphatic carboxylic acid series are recorded.


Author(s):  
K. A. Andrianov ◽  
A. K. Dabagova ◽  
V. V. Shokina ◽  
I. L. Knunyants

Author(s):  
Ratnamala P. Sonawane ◽  
Rahul R. Tripathi

Isatins are synthetically versatile substrates, where they can be used for the synthesis of a large variety of heterocyclic compounds. In this, a convenient method has been developed for the conversion of Indoles into Isatins and some heterocyclic derivative were synthesised such as 5- nitro-1H-indole-2,3-dione, 2-methylquinoline-4-carboxylic acid which may be used as raw material for drug synthesis. The general process utilizes the effective method for synthesis of Isatin from Indole is bromination and oxidation with an N-bromosuccinimide-dimethyl sulfoxide reagent. The nitration of Isatin at C-5 takes place by using KNO3, conc. H2SO4, 2-methylquinoline-4-caboxylic acid are usually obtained from pfitzinger reaction.


1976 ◽  
Vol 5 (12) ◽  
pp. 1407-1408 ◽  
Author(s):  
Nobuo Ishikawa ◽  
Shigekuni Sasaki

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