HIGHLY STEREOSELECTIVE ALKYLATION REACTION OF ESTER ENOLATES GENERATED FROM δ-HYDROXY CARBOXYLIC ACID ESTERS

1986 ◽  
Vol 15 (1) ◽  
pp. 81-84 ◽  
Author(s):  
Koichi Narasaka ◽  
Yutaka Ukaji
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.


ChemInform ◽  
2010 ◽  
Vol 27 (33) ◽  
pp. no-no
Author(s):  
L. JEANNIN ◽  
J. SAPI ◽  
E. VASSILEVA ◽  
P. RENARD ◽  
J.-Y. LARONZE
Keyword(s):  

ChemSusChem ◽  
2013 ◽  
Vol 7 (2) ◽  
pp. 644-649 ◽  
Author(s):  
Ursula Biermann ◽  
Jürgen O. Metzger
Keyword(s):  

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