Chiral pentaisopropylcyclopentadienyl and pentakis(1-ethylpropyl)cyclopentadienyl complexes: one-pot synthesis by formation of 10 carbon-carbon bonds from pentamethylcobalticinium

1990 ◽  
Vol 112 (11) ◽  
pp. 4607-4609 ◽  
Author(s):  
Bruno Gloaguen ◽  
Didier Astruc
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.


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

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