RT Journal Article
T1 An Expedient Regio- and Diastereoselective Synthesis of Hybrid Frameworks with Embedded Spiro[9,10]dihydroanthracene [9,3′]-pyrrolidine and Spiro[oxindole-3,2′-pyrrolidine] Motifs via an Ionic Liquid-Mediated Multicomponent Reaction
A1 Arumugam, Natarajan
A1 Almansour, Abdulrahman
A1 Kumar, Raju
A1 Menéndez Ramos, José Carlos
A1 Sultan, Mujeeb
A1 Karama, Usama
A1 Ghabbour, Hazem
A1 Fun, Hoong-Kun
AB A series of hitherto unreported anthracene-embedded dispirooxindoles has been synthesized via a one-pot three-component 1,3-dipolar cycloaddition reaction of an azomethine ylide, generated in situ from the reaction of isatin and sarcosine to 10-benzylideneanthracen9(10H)-one as a dipolarophile in 1-butyl-3-methylimidazolium bromide([bmim]Br), an ionic liquid. This reaction proceeded regio- and diastereoselectively, in good to excellent yields.
PB MDPI
SN 1420-3049
YR 2015
FD 2015-09-03
LK https://hdl.handle.net/20.500.14352/23898
UL https://hdl.handle.net/20.500.14352/23898
LA eng
NO Deanship of Scientific Research at King Saud University
DS Docta Complutense
RD 23 ago 2024