Novel bisimidazolium pincers as low loading ligands for in situ palladium-catalyzed Suzuki-Miyaura reaction in the ambient atmosphere

Chao Gao; Hongjun Zhou; Siping Wei; Yinsong Zhao; Jingsong You; Ge Gao

doi:10.1039/c2cc36375e

Novel bisimidazolium pincers as low loading ligands for in situ palladium-catalyzed Suzuki-Miyaura reaction in the ambient atmosphere

Chao Gao
, Hongjun Zhou
, Siping Wei
, Yinsong Zhao
, Jingsong You
, Ge Gao^*

^*Corresponding author for this work

Sichuan University

Research output: Contribution to journal › Article › peer-review

27 Scopus citations

Abstract

A series of novel triazinonide-bridged bisimidazolium pincers were easily synthesized by quaternization of functionalized N-phenylimidazoles with highly reactive cyanuric chloride under mild conditions. The pincer 3c was proven to be a very efficient ligand for in situ Pd-catalyzed Suzuki-Miyaura reaction with ppm-level catalyst loading.

Original language	English
Pages (from-to)	1127-1129
Number of pages	3
Journal	Chemical Communications
Volume	49
Issue number	11
DOIs	https://doi.org/10.1039/c2cc36375e
State	Published - 10 Jan 2013
Externally published	Yes

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10.1039/c2cc36375e

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title = "Novel bisimidazolium pincers as low loading ligands for in situ palladium-catalyzed Suzuki-Miyaura reaction in the ambient atmosphere",

abstract = "A series of novel triazinonide-bridged bisimidazolium pincers were easily synthesized by quaternization of functionalized N-phenylimidazoles with highly reactive cyanuric chloride under mild conditions. The pincer 3c was proven to be a very efficient ligand for in situ Pd-catalyzed Suzuki-Miyaura reaction with ppm-level catalyst loading.",

author = "Chao Gao and Hongjun Zhou and Siping Wei and Yinsong Zhao and Jingsong You and Ge Gao",

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T1 - Novel bisimidazolium pincers as low loading ligands for in situ palladium-catalyzed Suzuki-Miyaura reaction in the ambient atmosphere

AU - Gao, Chao

AU - Zhou, Hongjun

AU - Wei, Siping

AU - Zhao, Yinsong

AU - You, Jingsong

AU - Gao, Ge

PY - 2013/1/10

Y1 - 2013/1/10

N2 - A series of novel triazinonide-bridged bisimidazolium pincers were easily synthesized by quaternization of functionalized N-phenylimidazoles with highly reactive cyanuric chloride under mild conditions. The pincer 3c was proven to be a very efficient ligand for in situ Pd-catalyzed Suzuki-Miyaura reaction with ppm-level catalyst loading.

AB - A series of novel triazinonide-bridged bisimidazolium pincers were easily synthesized by quaternization of functionalized N-phenylimidazoles with highly reactive cyanuric chloride under mild conditions. The pincer 3c was proven to be a very efficient ligand for in situ Pd-catalyzed Suzuki-Miyaura reaction with ppm-level catalyst loading.

UR - https://www.scopus.com/pages/publications/84872178234

U2 - 10.1039/c2cc36375e

DO - 10.1039/c2cc36375e

M3 - 文章

C2 - 23283182

AN - SCOPUS:84872178234

SN - 1359-7345

VL - 49

SP - 1127

EP - 1129

JO - Chemical Communications

JF - Chemical Communications

IS - 11

ER -

Novel bisimidazolium pincers as low loading ligands for in situ palladium-catalyzed Suzuki-Miyaura reaction in the ambient atmosphere

Abstract

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