Li-Jun Geng
Hebei University
17 Papers
44 Citations
Li-Jun Geng is an academic researcher from Hebei University. The author has contributed to research in topics: 1,3-Dipolar cycloaddition & Pyridine. The author has an hindex of 5, co-authored 17 publications. Previous affiliations of Li-Jun Geng include Tianjin University & Hebei University of Science and Technology.
Chat about Author
Papers
Multicomponent Reaction for Synthesis of 2-(Indol-3-yl)pyridine Derivatives Under Microwave Irradiation
TL;DR: In this article, a short, practical, and efficient preparation of 2-(indol-3-yl)pyridine derivatives via a one-pot procedure of 3-cyanoacetylindole, chalcones, and ammonium acetate under microwave irradiation was described.
10
Synthesis of α, α, -bis(substitutedbenzylidene) cycloalkanones by a grinding method
TL;DR: In this paper, the crossed aldol condensation of various aromatic aldehydes with cycloalkanones was studied under solvent free conditions by a grinding method at room temperature.
9
One-pot, three-component route to spiropyrrolidine derivatives via a 1,3-dipolar cycloaddition reaction
TL;DR: In this paper, a series of spiropyrrolidine derivatives were synthesized via three-component 1,3-dipolar cycloaddition reactions of 1-(1-methylpyrrole-2-yl)-3-aryl, 2-cyano-1-propenones, isatin and sarcosine in refluxing methanol.
7
Synthesis and optical properties of novel compounds containing carbazole and 1, 8-naphthalimide groups:
TL;DR: A series of novel carbazole-naphthalimide compounds with moieties capable of carrier-balance and electroluminescence were synthesised and characterised, and their luminescent properties had been s...
6
A facile synthesis of dispiro[indole-3,2'-pyrrolidine-3,5''-[1,3]thiazolane] derivatives from 2,3,5-trisubstituted-4-thiazolidinones via 1,3-dipolar cycloaddition reaction
TL;DR: A series of 2″,3″,4′-triaryl-1′-methyldispiro derivatives were successfully synthesised via a three-component 1,3-dipolar cycloaddition reaction of 2,3,5-trisubstituted-4-thiazolidinones, isatin and sarcosine in refluxing toluene to provide access to a fast one-pot synthesis of spiroheterocycle in high yields.
5