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Synthesis and spectroscopic properties of rotamers in the series of 2-(fluoroaryl)-4-substituted pyrroles
•A mild, simple and efficient method for the synthesis of fluroaryl substituted pyrroles was elabotated.•All ortho-fluroaryl substituted pyrroles contains double sets signals in 13C NMR spectra.•Based on the combination of 2D HMBC and HSQC NMR spectroscopy, as well as temperature dependent NMR exper...
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Published in: | Journal of fluorine chemistry 2021-09, Vol.249, p.109863, Article 109863 |
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creator | Miftyakhova, Almira R. Matveeva, Maria D. Zhilyaev, Dmitry I. Eltsov, Oleg S. Talarico, Giovanni Smol'yakov, Alexander F. Voskressensky, Leonid G. Efimov, Ilya V. |
description | •A mild, simple and efficient method for the synthesis of fluroaryl substituted pyrroles was elabotated.•All ortho-fluroaryl substituted pyrroles contains double sets signals in 13C NMR spectra.•Based on the combination of 2D HMBC and HSQC NMR spectroscopy, as well as temperature dependent NMR experiments in DMSO and CDCl3 we conclude that the ratio of obtained rotamers does not depends on the nature of the solvent and temperature.
A mild, simple and efficient method for the synthesis of ortho, meta and para-fluoroaryl substituted pyrroles was discovered. It was found by NMR spectroscopy, that ortho-fluoroaryl substituted pyrroles exist in the form of inhibited conformational isomers (rotamers). Intramolecular interaction of the hydrogen atom of the pyrrole ring and the fluorine atom in the ortho-position of the aryl substituent leads to the appearance of two sets of signals in the 1H and 13C NMR spectra. Based on the combination of 2D HMBC and HSQC NMR spectroscopy, as well as temperature dependent NMR experiments in DMSO and CDCl3 we conclude that the ratio of obtained rotamers is permanent and does not depend from the temperature.
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A mild, simple and efficient method for the synthesis of ortho, meta and para-fluoroaryl substituted pyrroles was discovered. It was found by NMR spectroscopy, that ortho-fluoroaryl substituted pyrroles exist in the form of inhibited conformational isomers (rotamers). Intramolecular interaction of the hydrogen atom of the pyrrole ring and the fluorine atom in the ortho-position of the aryl substituent leads to the appearance of two sets of signals in the 1H and 13C NMR spectra. Based on the combination of 2D HMBC and HSQC NMR spectroscopy, as well as temperature dependent NMR experiments in DMSO and CDCl3 we conclude that the ratio of obtained rotamers is permanent and does not depend from the temperature.
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Fonts or abstract dimensions should not be changed or altered. [Display omitted]</description><identifier>ISSN: 0022-1139</identifier><identifier>EISSN: 1873-3328</identifier><identifier>DOI: 10.1016/j.jfluchem.2021.109863</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Cycloaddition ; Enamine ; Enaminone ; Fluorine ; Isocyanide ; Isomers ; Magnetic resonance spectroscopy ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; Pyrrole ; Pyrroles ; Rotamers ; Spectroscopy ; Spectrum analysis ; Substitutes ; Synthesis ; Temperature dependence</subject><ispartof>Journal of fluorine chemistry, 2021-09, Vol.249, p.109863, Article 109863</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright Elsevier BV Sep 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-4551a90eaf417c83a95f4ecd1800e4007b06799e0a96b95f7aadb072152e69ea3</citedby><cites>FETCH-LOGICAL-c340t-4551a90eaf417c83a95f4ecd1800e4007b06799e0a96b95f7aadb072152e69ea3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Miftyakhova, Almira R.</creatorcontrib><creatorcontrib>Matveeva, Maria D.</creatorcontrib><creatorcontrib>Zhilyaev, Dmitry I.</creatorcontrib><creatorcontrib>Eltsov, Oleg S.</creatorcontrib><creatorcontrib>Talarico, Giovanni</creatorcontrib><creatorcontrib>Smol'yakov, Alexander F.</creatorcontrib><creatorcontrib>Voskressensky, Leonid G.</creatorcontrib><creatorcontrib>Efimov, Ilya V.</creatorcontrib><title>Synthesis and spectroscopic properties of rotamers in the series of 2-(fluoroaryl)-4-substituted pyrroles</title><title>Journal of fluorine chemistry</title><description>•A mild, simple and efficient method for the synthesis of fluroaryl substituted pyrroles was elabotated.•All ortho-fluroaryl substituted pyrroles contains double sets signals in 13C NMR spectra.•Based on the combination of 2D HMBC and HSQC NMR spectroscopy, as well as temperature dependent NMR experiments in DMSO and CDCl3 we conclude that the ratio of obtained rotamers does not depends on the nature of the solvent and temperature.
A mild, simple and efficient method for the synthesis of ortho, meta and para-fluoroaryl substituted pyrroles was discovered. It was found by NMR spectroscopy, that ortho-fluoroaryl substituted pyrroles exist in the form of inhibited conformational isomers (rotamers). Intramolecular interaction of the hydrogen atom of the pyrrole ring and the fluorine atom in the ortho-position of the aryl substituent leads to the appearance of two sets of signals in the 1H and 13C NMR spectra. Based on the combination of 2D HMBC and HSQC NMR spectroscopy, as well as temperature dependent NMR experiments in DMSO and CDCl3 we conclude that the ratio of obtained rotamers is permanent and does not depend from the temperature.
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[Display omitted]</description><subject>Cycloaddition</subject><subject>Enamine</subject><subject>Enaminone</subject><subject>Fluorine</subject><subject>Isocyanide</subject><subject>Isomers</subject><subject>Magnetic resonance spectroscopy</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>Pyrrole</subject><subject>Pyrroles</subject><subject>Rotamers</subject><subject>Spectroscopy</subject><subject>Spectrum analysis</subject><subject>Substitutes</subject><subject>Synthesis</subject><subject>Temperature dependence</subject><issn>0022-1139</issn><issn>1873-3328</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkE9LxDAQxYMouK5-BQl40UPXSdKm7U1Z_AcLHtRzSNMpm7Lb1CQV9tubZdezp4GZeTPv_Qi5ZrBgwOR9v-i7zWTWuF1w4Cw160qKEzJjVSkyIXh1SmYAnGeMifqcXITQA0AJZTUj9mM3xDUGG6geWhpGNNG7YNxoDR29G9FHi4G6jnoX9RZ9oHagSUID-uOEZ7fJgfNO-93mLsuzMDUh2jhFbOm4895tMFySs05vAl4d65x8PT99Ll-z1fvL2_JxlRmRQ8zyomC6BtRdzkpTCV0XXY6mZRUA5sl2A7KsawRdyybNSq3bBkrOCo6yRi3m5OZwN7n_njBE1bvJD-ml4kUphZRFLtKWPGyZlDZ47NTo7Tb5VwzUHqvq1R9WtceqDliT8OEgxJThx6JXwVgcDLbWJ3aqdfa_E79rC4V3</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Miftyakhova, Almira R.</creator><creator>Matveeva, Maria D.</creator><creator>Zhilyaev, Dmitry I.</creator><creator>Eltsov, Oleg S.</creator><creator>Talarico, Giovanni</creator><creator>Smol'yakov, Alexander F.</creator><creator>Voskressensky, Leonid G.</creator><creator>Efimov, Ilya V.</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>7U7</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope></search><sort><creationdate>202109</creationdate><title>Synthesis and spectroscopic properties of rotamers in the series of 2-(fluoroaryl)-4-substituted pyrroles</title><author>Miftyakhova, Almira R. ; 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A mild, simple and efficient method for the synthesis of ortho, meta and para-fluoroaryl substituted pyrroles was discovered. It was found by NMR spectroscopy, that ortho-fluoroaryl substituted pyrroles exist in the form of inhibited conformational isomers (rotamers). Intramolecular interaction of the hydrogen atom of the pyrrole ring and the fluorine atom in the ortho-position of the aryl substituent leads to the appearance of two sets of signals in the 1H and 13C NMR spectra. Based on the combination of 2D HMBC and HSQC NMR spectroscopy, as well as temperature dependent NMR experiments in DMSO and CDCl3 we conclude that the ratio of obtained rotamers is permanent and does not depend from the temperature.
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subjects | Cycloaddition Enamine Enaminone Fluorine Isocyanide Isomers Magnetic resonance spectroscopy NMR NMR spectroscopy Nuclear magnetic resonance Pyrrole Pyrroles Rotamers Spectroscopy Spectrum analysis Substitutes Synthesis Temperature dependence |
title | Synthesis and spectroscopic properties of rotamers in the series of 2-(fluoroaryl)-4-substituted pyrroles |
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