Suzuki–Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-Di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) palladium complex

Suzuki–Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-Di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) palladium complex

A 1,4-di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr)-based PEPPSI-type palladium complex was developed as an excellent precatalyst for the Suzuki–Miyaura cross-coupling reaction. The complex showed high activity under mild conditions for the cross-coupling reactions between various types...

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Main Authors: Huang, Jie, Hong, Jong-Tai, Hong, Soon Hyeok
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/101911
http://hdl.handle.net/10220/11201
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1019112020-03-07T12:34:54Z Suzuki–Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-Di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) palladium complex Huang, Jie Hong, Jong-Tai Hong, Soon Hyeok School of Physical and Mathematical Sciences A 1,4-di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr)-based PEPPSI-type palladium complex was developed as an excellent precatalyst for the Suzuki–Miyaura cross-coupling reaction. The complex showed high activity under mild conditions for the cross-coupling reactions between various types of aryl chlorides and aryl boronic acids regardless of the steric and electronic nature of the substrates. 2013-07-11T06:03:39Z 2019-12-06T20:46:33Z 2013-07-11T06:03:39Z 2019-12-06T20:46:33Z 2012 2012 Journal Article Huang, J., Hong, J.-T., & Hong, S. H. (2012). Suzuki–Miyaura Cross-Coupling Reaction Catalyzed by PEPPSI-Type 1,4-Di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) Palladium Complex. European Journal of Organic Chemistry, 2012(33), 6630-6635. https://hdl.handle.net/10356/101911 http://hdl.handle.net/10220/11201 10.1002/ejoc.201201075 en European journal of organic chemistry © 2012 Wiley-VCH Verlag GmbH 6630 & Co. KGaA, Weinheim
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
description A 1,4-di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr)-based PEPPSI-type palladium complex was developed as an excellent precatalyst for the Suzuki–Miyaura cross-coupling reaction. The complex showed high activity under mild conditions for the cross-coupling reactions between various types of aryl chlorides and aryl boronic acids regardless of the steric and electronic nature of the substrates.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Huang, Jie
Hong, Jong-Tai
Hong, Soon Hyeok
format Article
author Huang, Jie
Hong, Jong-Tai
Hong, Soon Hyeok
spellingShingle Huang, Jie
Hong, Jong-Tai
Hong, Soon Hyeok
Suzuki–Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-Di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) palladium complex
author_sort Huang, Jie
title Suzuki–Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-Di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) palladium complex
title_short Suzuki–Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-Di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) palladium complex
title_full Suzuki–Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-Di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) palladium complex
title_fullStr Suzuki–Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-Di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) palladium complex
title_full_unstemmed Suzuki–Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-Di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) palladium complex
title_sort suzuki–miyaura cross-coupling reaction catalyzed by peppsi-type 1,4-di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzipr) palladium complex
publishDate 2013
url https://hdl.handle.net/10356/101911
http://hdl.handle.net/10220/11201
_version_ 1681039234716139520

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