RT Journal Article
T1 A Sustainable Approach to the Stereoselective Synthesis of Diazaheptacyclic Cage Systems Based on a Multicomponent Strategy in an Ionic Liquid
A1 Suresh Kumar, Raju
A1 Almansour, Abdulrahman
A1 Arumugam, Natarajan
A1 Altaf, Mohammad
A1 Menéndez Ramos, José Carlos
A1 Kumar, Raju
A1 Osman, Hasnah
AB The microwave-assisted three-component reactions of 3,5-bis(E)-arylmethylidene] tetrahydro-4(1H)-pyridinones, acenaphthenequinone and cyclic α-amino acids in an ionic liquid, 1-butyl-3-methylimidazolium bromide, occurred through a domino sequence affording structurally intriguing diazaheptacyclic cage-like compounds in excellent yields.
PB MDPI
SN 1420-3049
YR 2016
FD 2016
LK https://hdl.handle.net/20.500.14352/23900
UL https://hdl.handle.net/20.500.14352/23900
LA eng
NO Deanship of Scientific Research at King Saud University
DS Docta Complutense
RD 9 abr 2025