A one pot, metathesis–hydrogenation sequence for the selective formation of carbon–carbon bonds

2005 ◽  
pp. 5544 ◽  
Author(s):  
Andrea J. Robinson ◽  
Jomana Elaridi ◽  
Jim Patel ◽  
W. Roy Jackson
ChemInform ◽  
2006 ◽  
Vol 37 (11) ◽  
Author(s):  
Andrea J. Robinson ◽  
Jomana Elaridi ◽  
Jim Patel ◽  
W. Roy Jackson

2016 ◽  
Vol 12 ◽  
pp. 1153-1169 ◽  
Author(s):  
Nivesh Kumar ◽  
Santanu Ghosh ◽  
Subhajit Bhunia ◽  
Alakesh Bisai

The synthesis of a variety of 2-oxindoles bearing an all-carbon quaternary center at the pseudo benzylic position has been achieved via a ‘transition-metal-free’ intramolecular dehydrogenative coupling (IDC). The construction of 2-oxindole moieties was carried out through formation of carbon–carbon bonds using KOt-Bu-catalyzed one pot C-alkylation of β-N-arylamido esters with alkyl halides followed by a dehydrogenative coupling. Experimental evidences indicated toward a radical-mediated path for this reaction.


1993 ◽  
Vol 115 (26) ◽  
pp. 12635-12636 ◽  
Author(s):  
Masaru Takayanagi ◽  
Nobuharu Umamori ◽  
Keiji Tanino ◽  
Isao Kuwajima

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