105357-90-2Relevant academic research and scientific papers
Efficient synthesis of substituted pyrroles through iron-mediated oxidation reaction of 3-methylenehexane-2,5-dione with primary amines
Chen, Xi,Yuan, JiaCheng,Zhou, Min
, p. 32 - 38 (2018/12/11)
An efficient route has been developed for the synthesis of multiple substituted pyrrole derivatives from the readily available agents through iron-mediated oxidative aromatization process in good to excellent yields. This method is well tolerated with a diverse broad range of substrates and a complementary approach to currently available synthetic methods.
Efficient synthesis of highly substituted pyrroles through a Pd(OCOCF 3)2-catalyzed cascade reaction of 2-alkenal-1,3-dicarbonyl compounds with primary amines
Yang, Wei,Huang, Liliang,Liu, Hong,Wang, Wei,Li, Hao
, p. 4667 - 4669 (2013/06/05)
We describe an unprecedented Pd(OCOCF3)2-catalyzed cascade process for the synthesis of highly functionalized 1,2,3,5- tetrasubstituted pyrroles with high efficiency. Unlike documented methods relying on preformed enamines and active halogenated terminal alkenes, the process employs simple 2-alkenal-dicarbonyls and primary amines in 'one-pot'. The Royal Society of Chemistry 2013.
Photochromic Heterocyclic Fulgides. Part 5. Rearrangement Reactions of (E)-α-1,2,5-Trimethyl-3-pyrrylethylidene(isopropylidene)succinic Anhydride and Related Compounds
Harris, Stuart A.,Heller, Harry G.,Oliver, Stephen N.
, p. 3259 - 3262 (2007/10/02)
The pale yellow (E)-isopropylidene-succinic anhydride 3b undergoes a reversible photochemical reaction to give the deep blue 7,7a-dihydro-1,2,4,7,7,7a-hexamethylindole-5,6-dicarboxylic anhydride 4b which is thermall
