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Papers by Feng-Shou Liu
Organic Chemistry Frontiers, 2019
Rigid hindered N-heterocyclic carbene palladium complexes have been developed and exhibited high ... more Rigid hindered N-heterocyclic carbene palladium complexes have been developed and exhibited high activities for a variety of (hetero)aryl chlorides with (hetero)anilines and amines under aerobic conditions.
Applied Organometallic Chemistry, 2012
A series of salicylaldimine ligands were designed to promote palladium‐catalyzed Suzuki–Miyaura c... more A series of salicylaldimine ligands were designed to promote palladium‐catalyzed Suzuki–Miyaura cross‐coupling reaction. After a screening process, a ligand with a bulky 2,4‐di‐tert‐butyl substituent on the salicyaldehyde backbone and cyclohexylamine moiety was found to serve as a good combination for this reaction in aqueous solutions of DMF. The protocol demonstrated a significant advance in the efficiency of the cross‐coupling of aryl bromides and aryl chlorides with arylboronic acids to produce the desired biaryl products. Copyright © 2012 John Wiley & Sons, Ltd.
Organic Chemistry Frontiers, 2019
Rigid hindered N-heterocyclic carbene palladium complexes have been developed and exhibited high ... more Rigid hindered N-heterocyclic carbene palladium complexes have been developed and exhibited high activities for a variety of (hetero)aryl chlorides with (hetero)anilines and amines under aerobic conditions.
Applied Organometallic Chemistry, 2012
A series of salicylaldimine ligands were designed to promote palladium‐catalyzed Suzuki–Miyaura c... more A series of salicylaldimine ligands were designed to promote palladium‐catalyzed Suzuki–Miyaura cross‐coupling reaction. After a screening process, a ligand with a bulky 2,4‐di‐tert‐butyl substituent on the salicyaldehyde backbone and cyclohexylamine moiety was found to serve as a good combination for this reaction in aqueous solutions of DMF. The protocol demonstrated a significant advance in the efficiency of the cross‐coupling of aryl bromides and aryl chlorides with arylboronic acids to produce the desired biaryl products. Copyright © 2012 John Wiley & Sons, Ltd.