Highly Efficient Suzuki-Miyaura Coupling of Aryl Tosylates and Mesylates Catalyzed by Stable, Cost-Effective [1,3-Bis(diphenylphosphino)propane]nickel(II) Chloride [Ni(dppp)Cl2] with only 1 mol% Loading-Reference-Cited by-同舟云学术

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Highly Efficient Suzuki-Miyaura Coupling of Aryl Tosylates and Mesylates Catalyzed by Stable, Cost-Effective [1,3-Bis(diphenylphosphino)propane]nickel(II) Chloride [Ni(dppp)Cl2] with only 1 mol% Loading

Published:2011-01-19 Issue:2-3 Volume:353 Page:309-314
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Gao Han,Li You,Zhou Yi-Guo,Han Fu-She,Lin Ying-Jie

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/adsc.201000710/fullpdf

Reference59 articles.

1. Nonpeptidic Ligands for Peptide-Activated G Protein-Coupled Receptors

2. Selected Patented Cross-Coupling Reaction Technologies

3. Conjugated Polymers and Aromaticity

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1. Nickel-Catalyzed Suzuki Coupling of Phenols Enabled by SuFEx of Tosyl Fluoride;Molecules;2023-01-07

2. Air‐Stable Fe 3 O 4 @SiO 2 ‐EDTA‐Ni(0) as an Efficient Recyclable Magnetic Nanocatalyst for Effective Suzuki‐Miyaura and Heck Cross‐Coupling via Aryl Sulfamates and Carbamates;Applied Organometallic Chemistry;2020-05-18

3. Copper (II) Schiff base-graphene oxide composite as an efficient catalyst for Suzuki-Miyaura reaction;Chemical Physics;2019-01

4. Biaryls;Privileged Structures in Drug Discovery;2018-03-09

5. Oxidative Addition of Aryl Electrophiles to a Prototypical Nickel(0) Complex: Mechanism and Structure/Reactivity Relationships;Organometallics;2017-04-06

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