Organometallic chemistry and application of palladacycles in asymmetric hydrophosphination reactions
A number of palladacycles containing chiral chelating auxiliaries have been utilized as efficient catalysts for asymmetric hydrophosphination reactions. In all cases, the chiral auxiliaries remained coordinated to the palladium centres throughout the course of the reactions. Despite the presence of...
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sg-ntu-dr.10356-1622382022-10-11T01:12:39Z Organometallic chemistry and application of palladacycles in asymmetric hydrophosphination reactions Seah, Jeffery Wee Kiong Teo, Ronald Hong Xiang Leung, Pak-Hing School of Physical and Mathematical Sciences Science::Chemistry Chiral Auxiliaries Hydrophosphination A number of palladacycles containing chiral chelating auxiliaries have been utilized as efficient catalysts for asymmetric hydrophosphination reactions. In all cases, the chiral auxiliaries remained coordinated to the palladium centres throughout the course of the reactions. Despite the presence of a large quantity of powerful tertiary phosphines, which are known to be strong metal ion sequesters, the expected catalyst poisoning was rarely observed in these palladacycle catalyzed processes. This review highlights the unique stereoelectronic features and the important organometallic chemistry of palladacycle catalysts which are essential to their synthetic operations. Ministry of Education (MOE) We wish to acknowledge the research funding provided by Singapore Ministry of Education Academic Research Fund Tier I (Grant ID 2019-T1-001-094). 2022-10-11T01:12:39Z 2022-10-11T01:12:39Z 2021 Journal Article Seah, J. W. K., Teo, R. H. X. & Leung, P. (2021). Organometallic chemistry and application of palladacycles in asymmetric hydrophosphination reactions. Dalton Transactions, 50(46), 16909-16915. https://dx.doi.org/10.1039/d1dt03134a 1477-9226 https://hdl.handle.net/10356/162238 10.1039/d1dt03134a 34734619 2-s2.0-85120674421 46 50 16909 16915 en 2019- T1-001-094 Dalton Transactions © 2021 The Royal Society of Chemistry. All rights reserved. |
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Science::Chemistry Chiral Auxiliaries Hydrophosphination Seah, Jeffery Wee Kiong Teo, Ronald Hong Xiang Leung, Pak-Hing Organometallic chemistry and application of palladacycles in asymmetric hydrophosphination reactions |
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A number of palladacycles containing chiral chelating auxiliaries have been utilized as efficient catalysts for asymmetric hydrophosphination reactions. In all cases, the chiral auxiliaries remained coordinated to the palladium centres throughout the course of the reactions. Despite the presence of a large quantity of powerful tertiary phosphines, which are known to be strong metal ion sequesters, the expected catalyst poisoning was rarely observed in these palladacycle catalyzed processes. This review highlights the unique stereoelectronic features and the important organometallic chemistry of palladacycle catalysts which are essential to their synthetic operations. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Seah, Jeffery Wee Kiong Teo, Ronald Hong Xiang Leung, Pak-Hing |
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Article |
author |
Seah, Jeffery Wee Kiong Teo, Ronald Hong Xiang Leung, Pak-Hing |
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Seah, Jeffery Wee Kiong |
title |
Organometallic chemistry and application of palladacycles in asymmetric hydrophosphination reactions |
title_short |
Organometallic chemistry and application of palladacycles in asymmetric hydrophosphination reactions |
title_full |
Organometallic chemistry and application of palladacycles in asymmetric hydrophosphination reactions |
title_fullStr |
Organometallic chemistry and application of palladacycles in asymmetric hydrophosphination reactions |
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Organometallic chemistry and application of palladacycles in asymmetric hydrophosphination reactions |
title_sort |
organometallic chemistry and application of palladacycles in asymmetric hydrophosphination reactions |
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2022 |
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https://hdl.handle.net/10356/162238 |
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