Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Journal of fluorine chemistry 2021-09, Vol.249, p.109863, Article 109863
Main Authors: Miftyakhova, Almira R., Matveeva, Maria D., Zhilyaev, Dmitry I., Eltsov, Oleg S., Talarico, Giovanni, Smol'yakov, Alexander F., Voskressensky, Leonid G., Efimov, Ilya V.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c340t-4551a90eaf417c83a95f4ecd1800e4007b06799e0a96b95f7aadb072152e69ea3
cites cdi_FETCH-LOGICAL-c340t-4551a90eaf417c83a95f4ecd1800e4007b06799e0a96b95f7aadb072152e69ea3
container_end_page
container_issue
container_start_page 109863
container_title Journal of fluorine chemistry
container_volume 249
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. To create your abstract, type over the instructions in the template box below. Fonts or abstract dimensions should not be changed or altered. [Display omitted]
doi_str_mv 10.1016/j.jfluchem.2021.109863
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2576366543</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S002211392100141X</els_id><sourcerecordid>2576366543</sourcerecordid><originalsourceid>FETCH-LOGICAL-c340t-4551a90eaf417c83a95f4ecd1800e4007b06799e0a96b95f7aadb072152e69ea3</originalsourceid><addsrcrecordid>eNqFkE9LxDAQxYMouK5-BQl40UPXSdKm7U1Z_AcLHtRzSNMpm7Lb1CQV9tubZdezp4GZeTPv_Qi5ZrBgwOR9v-i7zWTWuF1w4Cw160qKEzJjVSkyIXh1SmYAnGeMifqcXITQA0AJZTUj9mM3xDUGG6geWhpGNNG7YNxoDR29G9FHi4G6jnoX9RZ9oHagSUID-uOEZ7fJgfNO-93mLsuzMDUh2jhFbOm4895tMFySs05vAl4d65x8PT99Ll-z1fvL2_JxlRmRQ8zyomC6BtRdzkpTCV0XXY6mZRUA5sl2A7KsawRdyybNSq3bBkrOCo6yRi3m5OZwN7n_njBE1bvJD-ml4kUphZRFLtKWPGyZlDZ47NTo7Tb5VwzUHqvq1R9WtceqDliT8OEgxJThx6JXwVgcDLbWJ3aqdfa_E79rC4V3</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2576366543</pqid></control><display><type>article</type><title>Synthesis and spectroscopic properties of rotamers in the series of 2-(fluoroaryl)-4-substituted pyrroles</title><source>ScienceDirect Journals</source><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.</creator><creatorcontrib>Miftyakhova, Almira R. ; Matveeva, Maria D. ; Zhilyaev, Dmitry I. ; Eltsov, Oleg S. ; Talarico, Giovanni ; Smol'yakov, Alexander F. ; Voskressensky, Leonid G. ; Efimov, Ilya V.</creatorcontrib><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. To create your abstract, type over the instructions in the template box below. 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. To create your abstract, type over the instructions in the template box below. Fonts or abstract dimensions should not be changed or altered. [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. ; Matveeva, Maria D. ; Zhilyaev, Dmitry I. ; Eltsov, Oleg S. ; Talarico, Giovanni ; Smol'yakov, Alexander F. ; Voskressensky, Leonid G. ; Efimov, Ilya V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-4551a90eaf417c83a95f4ecd1800e4007b06799e0a96b95f7aadb072152e69ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Cycloaddition</topic><topic>Enamine</topic><topic>Enaminone</topic><topic>Fluorine</topic><topic>Isocyanide</topic><topic>Isomers</topic><topic>Magnetic resonance spectroscopy</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>Pyrrole</topic><topic>Pyrroles</topic><topic>Rotamers</topic><topic>Spectroscopy</topic><topic>Spectrum analysis</topic><topic>Substitutes</topic><topic>Synthesis</topic><topic>Temperature dependence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts – Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of fluorine chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miftyakhova, Almira R.</au><au>Matveeva, Maria D.</au><au>Zhilyaev, Dmitry I.</au><au>Eltsov, Oleg S.</au><au>Talarico, Giovanni</au><au>Smol'yakov, Alexander F.</au><au>Voskressensky, Leonid G.</au><au>Efimov, Ilya V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and spectroscopic properties of rotamers in the series of 2-(fluoroaryl)-4-substituted pyrroles</atitle><jtitle>Journal of fluorine chemistry</jtitle><date>2021-09</date><risdate>2021</risdate><volume>249</volume><spage>109863</spage><pages>109863-</pages><artnum>109863</artnum><issn>0022-1139</issn><eissn>1873-3328</eissn><abstract>•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. To create your abstract, type over the instructions in the template box below. Fonts or abstract dimensions should not be changed or altered. [Display omitted]</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><doi>10.1016/j.jfluchem.2021.109863</doi></addata></record>
fulltext fulltext
identifier ISSN: 0022-1139
ispartof Journal of fluorine chemistry, 2021-09, Vol.249, p.109863, Article 109863
issn 0022-1139
1873-3328
language eng
recordid cdi_proquest_journals_2576366543
source ScienceDirect Journals
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T22%3A30%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20spectroscopic%20properties%20of%20rotamers%20in%20the%20series%20of%202-(fluoroaryl)-4-substituted%20pyrroles&rft.jtitle=Journal%20of%20fluorine%20chemistry&rft.au=Miftyakhova,%20Almira%20R.&rft.date=2021-09&rft.volume=249&rft.spage=109863&rft.pages=109863-&rft.artnum=109863&rft.issn=0022-1139&rft.eissn=1873-3328&rft_id=info:doi/10.1016/j.jfluchem.2021.109863&rft_dat=%3Cproquest_cross%3E2576366543%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c340t-4551a90eaf417c83a95f4ecd1800e4007b06799e0a96b95f7aadb072152e69ea3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2576366543&rft_id=info:pmid/&rfr_iscdi=true