Stereoselective electrocatalytic cyclization of 3-substituted 2,2-dicyanocyclopropane-1,1-dicarboxylic acid esters to form 6-substituted (1R,5R,6R)*-4,4-dialkoxy-5-cyano-2-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic acid esters

2006 ◽  
Vol 55 (1) ◽  
pp. 106-111 ◽  
Author(s):  
M. N. Elinson ◽  
S. K. Fedukovich ◽  
Z. A. Starikova ◽  
A. N. Vereshchagin ◽  
P. A. Belyakov ◽  
...  
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.


1999 ◽  
Vol 23 (3) ◽  
pp. 174-175
Author(s):  
E. Abdel-Ghani

The orientation of cyclization of the reaction of methyl aroylacrylate (1) and aroylacrylic acid (8) with ethyl acetoacetate and/or thiourea leading to the formation of 4-aroylmethylcyclopentane-1,3-dione (2) 5-aryl-3-oxocyclohexene-1,2-dicarboxylic acid (9), 2-imino-5-aroylmethylthiazolidin-4-one (11) and 6-aryl-2-sulfonylpyrimidine-4-carboxylic acid (14) depends on the medium employed; some compounds show moderate antiviral activities against tobacco necrosis virus.


2007 ◽  
Vol 77 (6) ◽  
pp. 1069-1077 ◽  
Author(s):  
V. E. Kataev ◽  
A. P. Timosheva ◽  
A. I. Nugmanov ◽  
A. T. Gubaidullin ◽  
I. Yu. Strobykina ◽  
...  

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):  

Sign in / Sign up

Export Citation Format

Share Document