1245604-22-1Relevant articles and documents
Efficient synthesis of isoindoles using supercritical carbon dioxide
Ito, Satoshi,Akaki, Masayuki,Shinozaki, Yasutaka,Iwabe, Yuuki,Furuya, Masaru,Tobata, Marina,Roppongi, Makoto,Sato, Takafumi,Itoh, Naotsugu,Oba, Toru
, p. 1338 - 1342 (2017)
Bicyclopyrroles were efficiently converted to the corresponding isoindoles by a retro Diels-Alder reaction in supercritical carbon dioxide. By adding ethylene gas as an oxygen scavenger, the isoindole yield was further improved.
Palladium-catalysed synthesis of 1-isoindolecarboxylic acid esters and sequential Diels-Alder reactions: Access to bridged- and fused-ring heterocycles
Sole, Daniel,Serrano, Olga
supporting information; experimental part, p. 3382 - 3384 (2010/01/06)
The Pd-catalysed intramolecular α-arylation of α-amino acid esters provides a useful methodology for the synthesis of substituted isoindole derivatives, which have been used in Diels-Alder reactions to access diverse skeletal frameworks.