39087-82-6Relevant academic research and scientific papers
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.
Synthetic method for the preparation of 2-aminomethyl-1,3-diene derivatives through indium-mediated 1,3-butadien-2-ylation of imines
Seomoon, Dong,Jaemyung A.,Lee, Phil Ho
supporting information; experimental part, p. 2401 - 2404 (2009/10/10)
An efficient method for the preparation of a variety of 2-aminomethyl-1,3-dienes was developed through the reaction of imines with organoindium reagent generated in situ from indium and 1,3-dibromo-2-butyne. Three-component reactions of aldehydes, amines,
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
Catalytic Iodination of Aromatic Compounds via ortho-Palladated Complexes
Andrienko,Goncharov,Raida
, p. 79 - 81 (2007/10/03)
Reactions of azobenzene and its substituted derivatives with iodine in DMF in the presence of the PdI2/CuCl2 pair as catalyst under oxygen atmosphere at 70-100°C proceed regioselectively to yield ortho-iodo derivatives. Large amounts
