m-Carborane-C-carboxylic acid esters derived from some terpene alcohols, sterols, plant phenols, and oximes of natural carbonyl compounds

2008 ◽  
Vol 44 (9) ◽  
pp. 1305-1310 ◽  
Author(s):  
E. A. Dikusar ◽  
V. I. Potkin ◽  
N. G. Kozlov ◽  
A. P. Yuvchenko ◽  
M. P. Bei ◽  
...  
Synthesis ◽  
1988 ◽  
Vol 1988 (07) ◽  
pp. 537-538 ◽  
Author(s):  
George A. Olah ◽  
An-hsiang Wu ◽  
Omar Farooq ◽  
G. K. Surya Prakash

2004 ◽  
Vol 40 (5) ◽  
pp. 472-477 ◽  
Author(s):  
E. A. Dikusar ◽  
N. G. Kozlov ◽  
T. D. Zvereva ◽  
A. P. Yuvchenko ◽  
L. A. Mel’nichuk

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.


Sign in / Sign up

Export Citation Format

Share Document