1240195-10-1Relevant academic research and scientific papers
A synthesis of functionalized dihydro-1H-pyrroles from Nef-isocyanide adducts and enamines
Yavari, Issa,Hosseinpour, Reza,Pashazadeh, Ramin
, p. 1662 - 1666 (2012)
α-Ketoimidoyl chlorides, obtained from α-addition of acyl chlorides onto alkyl isocyanides, are treated with enamines to afford 5-(alkylimino)-4-hydroxy-4,5-dihydro-1H-pyrrole-2,3,4-tricarboxylates and 2-(alkylimino)-3-hydroxy-2,3-dihydro-1H-pyrrole-3,4-dicarboxylates in good to excellent yields. Georg Thieme Verlag Stuttgart · New York.
ZnO-nanoparticles as an efficient catalyst for the synthesis of tetrasubstituted cyclopentadienones using sulfonoketenimides and enaminoesters
Varasteh Moradi, Ali
, p. 45 - 49 (2018)
A convenient and efficient approach to the synthesis of substituted cyclopentadienes is reported based on the reaction of sulfonoketenimides and enaminoesters in good yield. In these reactions, sulfonoketenimides is produced from the reaction of terminal
The reaction of dialkyl acetylenedicarboxylates with 2-oxo-2- phenylacetaldehyde in the presence of primary amines: Synthesis of alkyl 2-benzoyl-4-alkylamino-5-oxo-2,5-dihydro-3-furan carboxylate derivatives
Safaei-Ghomi, Javad,Salimi, Fariba,Ramazani, Ali,Zeinali Nasrabadi, Fatemeh,Ahmadi, Yavar
experimental part, p. 485 - 492 (2012/05/31)
A 3-component domino reaction approach between a primary amine, a dialkyl acetylenedicarboxylate, and 2-oxo-2-phenylacetaldehyde that affords novel alkyl 2-benzoyl-4-alkylamino-5-oxo-2,5-dihydro-3-furan carboxylate derivatives is reported. The reaction se
Synthesis of indolequinones from bromoquinones and enamines mediated by Cu(OAc)2H2O
Inman, Martyn,Moody, Christopher J.
supporting information; experimental part, p. 6023 - 6026 (2010/11/20)
A Cu(II)-mediated synthesis of indolequinones from the corresponding bromoquinones and enamines is reported. The key oxidative cyclization proceeds in good yield for a broad range of substrates and can be performed on a multigram scale, allowing access to biologically interesting structures.
