Nickel-catalyzed divergent Mizoroki–Heck reaction of 1,3-dienes
Developing efficient strategies to realize divergent arylation of dienes has been a longstanding synthetic challenge. Herein, a nickel-catalyzed divergent Mizoroki–Heck reaction of 1,3-dienes has been demonstrated through the modification of ligands and additives.
Main Authors: | Wei-Song Zhang, Ding-Wei Ji, Ying Li, Xiang-Xin Zhang, Yong-Kang Mei, Bing-Zhi Chen, Qing-An Chen |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2023-02-01
|
Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-023-36237-1 |
Similar Items
-
The nickel-catalyzed Mizoroki-Heck reaction : high regioselectivity in Olefin migratory insertion and photoredox-enabled indoline formation
by: Tasker, Sarah Z. (Sarah Zinnen)
Published: (2016) -
Linear Polystyrene-Stabilized PdO Nanoparticle-Catalyzed Mizoroki-Heck Reactions in Water
by: Takuto Teratani, et al.
Published: (2011-10-01) -
Precise electrical gating of the single-molecule Mizoroki-Heck reaction
by: Lei Zhang, et al.
Published: (2022-08-01) -
Nickel-Catalyzed Heck Reaction
by: Pragya Gahlot, et al.
Published: (2023-03-01) -
Nickel-Catalyzed Mizoroki-Heck Reaction of Aryl Sulfonates and Chlorides with Electronically Unbiased Terminal Olefins: High Selectivity for Branched Products
by: Tasker, Sarah Z., et al.
Published: (2015)