1,3-Dipolar cycloaddition of azomethine ylides and imidoyl halides for synthesis of π-extended imidazolium salts
A new synthetic approach to π-extended imidazolium salts is developed based on 1,3-dipolar cycloaddition of polycyclic aromatic azomethine ylides with imidoyl chlorides, where the key to the successful conversion is the addition of cesium fluoride as an additive. Experimental and theoretical studies...
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sg-ntu-dr.10356-1628152023-02-28T20:09:41Z 1,3-Dipolar cycloaddition of azomethine ylides and imidoyl halides for synthesis of π-extended imidazolium salts Li, Qiang-Qiang Hamamoto, Yosuke Tan, Cheryl Cai Hui Sato, Hiroyasu Ito, Shingo School of Physical and Mathematical Sciences Science::Chemistry Aromatic Compounds 3-Dipolar Cycloaddition A new synthetic approach to π-extended imidazolium salts is developed based on 1,3-dipolar cycloaddition of polycyclic aromatic azomethine ylides with imidoyl chlorides, where the key to the successful conversion is the addition of cesium fluoride as an additive. Experimental and theoretical studies revealed that this cycloaddition proceeds via a stepwise mechanism rather than a concerted mechanism. This present method provides an efficient method to synthesize a variety of imidazolium-containing polycyclic aromatic compounds. Submitted/Accepted version 2022-11-10T02:18:48Z 2022-11-10T02:18:48Z 2022 Journal Article Li, Q., Hamamoto, Y., Tan, C. C. H., Sato, H. & Ito, S. (2022). 1,3-Dipolar cycloaddition of azomethine ylides and imidoyl halides for synthesis of π-extended imidazolium salts. Organic Chemistry Frontiers, 9(15), 4128-4134. https://dx.doi.org/10.1039/d2qo00941b 2052-4129 https://hdl.handle.net/10356/162815 10.1039/d2qo00941b 2-s2.0-85133628209 15 9 4128 4134 en Organic Chemistry Frontiers © 2022 the Partner Organisations. All rights reserved. This paper was published by Royal Society of Chemistry in Organic Chemistry Frontiers and is made available with permission of the Partner Organisations. application/pdf |
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Science::Chemistry Aromatic Compounds 3-Dipolar Cycloaddition Li, Qiang-Qiang Hamamoto, Yosuke Tan, Cheryl Cai Hui Sato, Hiroyasu Ito, Shingo 1,3-Dipolar cycloaddition of azomethine ylides and imidoyl halides for synthesis of π-extended imidazolium salts |
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A new synthetic approach to π-extended imidazolium salts is developed based on 1,3-dipolar cycloaddition of polycyclic aromatic azomethine ylides with imidoyl chlorides, where the key to the successful conversion is the addition of cesium fluoride as an additive. Experimental and theoretical studies revealed that this cycloaddition proceeds via a stepwise mechanism rather than a concerted mechanism. This present method provides an efficient method to synthesize a variety of imidazolium-containing polycyclic aromatic compounds. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Li, Qiang-Qiang Hamamoto, Yosuke Tan, Cheryl Cai Hui Sato, Hiroyasu Ito, Shingo |
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Article |
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Li, Qiang-Qiang Hamamoto, Yosuke Tan, Cheryl Cai Hui Sato, Hiroyasu Ito, Shingo |
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Li, Qiang-Qiang |
title |
1,3-Dipolar cycloaddition of azomethine ylides and imidoyl halides for synthesis of π-extended imidazolium salts |
title_short |
1,3-Dipolar cycloaddition of azomethine ylides and imidoyl halides for synthesis of π-extended imidazolium salts |
title_full |
1,3-Dipolar cycloaddition of azomethine ylides and imidoyl halides for synthesis of π-extended imidazolium salts |
title_fullStr |
1,3-Dipolar cycloaddition of azomethine ylides and imidoyl halides for synthesis of π-extended imidazolium salts |
title_full_unstemmed |
1,3-Dipolar cycloaddition of azomethine ylides and imidoyl halides for synthesis of π-extended imidazolium salts |
title_sort |
1,3-dipolar cycloaddition of azomethine ylides and imidoyl halides for synthesis of π-extended imidazolium salts |
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2022 |
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https://hdl.handle.net/10356/162815 |
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