39087-82-6Relevant articles and documents
Selective synthesis of either isoindole- or isoindoline-1-carboxylic acid esters by Pd(0)-catalyzed enolate arylation
Sole, Daniel,Serrano, Olga
supporting information; experimental part, p. 6267 - 6270 (2010/12/19)
Figure presented. Two efficient palladium-catalyzed intramolecular α-arylation reactions of α-amino acid esters have been developed that allow either 1-isoindolecarboxylic acid esters or the corresponding isoindolines to be selectively synthesized simply by a slight change of reaction conditions.
Palladium catalysed tandem cyclisation-anion capture processes. Part 8 [1]: In situ and preformed organostannanes. Carbamyl chlorides and other starter species
Anwar, Usman,Fielding, Mark R.,Grigg, Ronald,Sridharan, Visuvanathar,Urch, Christopher J.
, p. 1476 - 1487 (2007/10/03)
A sequential one-pot process is reported involving in situ, palladium catalysed, formation of a series of tributylstannyl-1,2-carbo and heterocyclic dialkylidene-5-membered rings from the corresponding 1,6-diynes and Bu 3SnH. These substrates a