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A series of pyrene derivatives featuring nonplanar structures of N,N-didodecylanilino-substituted donor and TCNE/TCNQ adduct acceptors have been efficiently synthesized via formal [2+2] cycloaddition.

Styrenic polymers P1(G0-CZ) and P2(G2-CZ) with carbazoles and carbazole containing dendrons as side chains were efficiently synthesized via "graft-to" approach by using copper-catalyzed azide/alkyne cycloaddition (CuAAC) reaction.

Lithium-selective (Li+) di-hydroxy crown ethers (CEs 3a 3h) were efficiently synthesized via intermolecular cyclization of bulky bis-epoxide with 1,2-dihydroxybenzene. Bis-epoxides were produced by etherifying allyl bromides with bulky diols to afford diene intermediates, which were subsequently epoxidized.

Water soluble molecular brush with poly(glycidyl methacrylate) (PGMA) as the main chain and mono-allyl terminated poly ethylene glycol) (PEG) as the densely grafted side chains was efficiently synthesized via grafting-onto approach by copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction.

Additionally, only simple clusters, such as dimers and trimers, have been efficiently synthesized.

Thermoresponsive copoly(β-thioether ester)s were efficiently synthesized from 2,5-furan diacrylate (2,5-FDA) via the thiol-Michael addition reaction under mild reaction conditions.

Ring B homolog of lithocholic acid (20) was efficiently synthesized.

Conclusion: The peptides were efficiently synthesized and the tested radiolabeling strategies showed successful results.

We reported NCNTs were efficiently synthesized on a lamellar vermiculite catalyst in a fluidized-bed reactor.

Novel ω-oxygenated vitamin K2 analogues were efficiently synthesized and their biological activities were evaluated.

The PU-H58-dimers 13a 15b were efficiently synthesized and their biological properties were evaluated.