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...
| Main Authors: | , , |
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| Other Authors: | |
| Format: | Journal Article |
| Language: | English |
| Published: |
2013
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| Online Access: | https://hdl.handle.net/10356/101911 http://hdl.handle.net/10220/11201 |
| _version_ | 1811684548714430464 |
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| author | Huang, Jie Hong, Jong-Tai Hong, Soon Hyeok |
| author2 | School of Physical and Mathematical Sciences |
| author_facet | School of Physical and Mathematical Sciences Huang, Jie Hong, Jong-Tai Hong, Soon Hyeok |
| author_sort | Huang, Jie |
| collection | NTU |
| 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. |
| first_indexed | 2024-10-01T04:30:23Z |
| format | Journal Article |
| id | ntu-10356/101911 |
| institution | Nanyang Technological University |
| language | English |
| last_indexed | 2024-10-01T04:30:23Z |
| publishDate | 2013 |
| record_format | dspace |
| spelling | ntu-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 |
| 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 |
| 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_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_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_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 |
| url | https://hdl.handle.net/10356/101911 http://hdl.handle.net/10220/11201 |
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