REACTIONS OF SODIUM SALICYLATE WITH MONOCHLOROACETIC ACID ESTERS

Author(s):  
Chinmurot Gulomovich Yodgorov ◽  
Tursunali Suyunovich Kholikov ◽  
Gulrukh Bakhodirovna Salieva ◽  
Shovkat Bakirovich Kholiyorov ◽  
Choriyor Eshmuminovich Usmanov
1980 ◽  
Vol 11 (40) ◽  
Author(s):  
A. E. EPSHTEIN ◽  
V. E. LIMANOV ◽  
M. YU. TELEGIN ◽  
E. K. SKVORTSOVA ◽  
T. I. MAXSIMOVA

Diabetes ◽  
2020 ◽  
Vol 69 (Supplement 1) ◽  
pp. 1832-P
Author(s):  
ANNA SANTORO ◽  
PENG ZHOU ◽  
YAN ZHU ◽  
ODILE D. PERONI ◽  
ANDREW T. NELSON ◽  
...  

2019 ◽  
Author(s):  
Jiang Wang ◽  
Brian P. Cary ◽  
Peyton Beyer ◽  
Samuel H. Gellman ◽  
Daniel Weix

A new strategy for the synthesis of ketones is presented based upon the decarboxylative coupling of N-hydroxyphthalimide (NHP) esters with S-2-pyridyl thioesters. The reactions are selective for the cross-coupled product because NHP esters act as radical donors and the thioesters act as acyl donors. The reaction conditions are general and mild, with over 40 examples presented, including larger fragments and the 20-mer peptide Exendin(9-39) on solid support.


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