Loading…

Vicinal halo-trifluoromethylation of alkenes

Both trifluoromethyl and halide groups are widely found in medicinally and pharmaceutically important compounds and, moreover, organohalides are commonly used as versatile intermediates in synthetic organic chemistry. Due to their prevalence and easy accessibility, alkene halo-trifluoromethylation p...

Full description

Saved in:
Bibliographic Details
Published in:RSC advances 2021-04, Vol.11 (25), p.14941-14955
Main Authors: Kareem, Rzgar Tawfeeq, Azizi, Bayan, Asnaashariisfahani, Manzarbanou, Ebadi, Abdolghaffar, Vessally, Esmail
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-c494t-bb69c1eb8729a0376701dee05f1e8cb3550105bc507783a96c77ef9529e6d1513
cites cdi_FETCH-LOGICAL-c494t-bb69c1eb8729a0376701dee05f1e8cb3550105bc507783a96c77ef9529e6d1513
container_end_page 14955
container_issue 25
container_start_page 14941
container_title RSC advances
container_volume 11
creator Kareem, Rzgar Tawfeeq
Azizi, Bayan
Asnaashariisfahani, Manzarbanou
Ebadi, Abdolghaffar
Vessally, Esmail
description Both trifluoromethyl and halide groups are widely found in medicinally and pharmaceutically important compounds and, moreover, organohalides are commonly used as versatile intermediates in synthetic organic chemistry. Due to their prevalence and easy accessibility, alkene halo-trifluoromethylation provides a convenient way to install these valuable functionalities in complex targets. In this review, we summarize recent advances and achievements in this fast-growing research field. For clarity, the reactions were classified according to the type of halogen atom. Both trifluoromethyl and halide groups are widely found in medicinally and pharmaceutically important compounds and, moreover, organohalides are commonly used as versatile intermediates in synthetic organic chemistry.
doi_str_mv 10.1039/d0ra06872a
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8698610</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2524205034</sourcerecordid><originalsourceid>FETCH-LOGICAL-c494t-bb69c1eb8729a0376701dee05f1e8cb3550105bc507783a96c77ef9529e6d1513</originalsourceid><addsrcrecordid>eNpdkc1LAzEQxYMottRevCsFLyKuTrJJdnMRSv0EQRD1GrJp1m5NNzXZFfrfG22t1bnMwPsxPN5DaB_DGYZUnI_BK-B5RtQW6hKgPCHAxfbG3UH9EKYQhzNMON5FnZRRQoGyLjp9qXRVKzuYKOuSxlelbZ13M9NMFlY1lasHrhwo-2ZqE_bQTqlsMP3V7qHn66un0W1y_3BzNxreJ5oK2iRFwYXGpoimhII04xngsTHASmxyXaSMAQZWaAZZlqdKcJ1lphSMCMPHmOG0hy6Wf-dtMTNjberGKyvnvpopv5BOVfKvUlcT-eo-ZM5FzmMsPXS8euDde2tCI2dV0MZaVRvXBkliEjzPKWURPfqHTl3rYyKRYoQSYJDSSJ0sKe1dCN6UazMY5FcP8hIeh989DCN8uGl_jf6kHoGDJeCDXqu_RaafJwWLeg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2524205034</pqid></control><display><type>article</type><title>Vicinal halo-trifluoromethylation of alkenes</title><source>PubMed Central</source><creator>Kareem, Rzgar Tawfeeq ; Azizi, Bayan ; Asnaashariisfahani, Manzarbanou ; Ebadi, Abdolghaffar ; Vessally, Esmail</creator><creatorcontrib>Kareem, Rzgar Tawfeeq ; Azizi, Bayan ; Asnaashariisfahani, Manzarbanou ; Ebadi, Abdolghaffar ; Vessally, Esmail</creatorcontrib><description>Both trifluoromethyl and halide groups are widely found in medicinally and pharmaceutically important compounds and, moreover, organohalides are commonly used as versatile intermediates in synthetic organic chemistry. Due to their prevalence and easy accessibility, alkene halo-trifluoromethylation provides a convenient way to install these valuable functionalities in complex targets. In this review, we summarize recent advances and achievements in this fast-growing research field. For clarity, the reactions were classified according to the type of halogen atom. Both trifluoromethyl and halide groups are widely found in medicinally and pharmaceutically important compounds and, moreover, organohalides are commonly used as versatile intermediates in synthetic organic chemistry.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/d0ra06872a</identifier><identifier>PMID: 35424045</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Alkenes ; Chemistry ; Organic chemistry</subject><ispartof>RSC advances, 2021-04, Vol.11 (25), p.14941-14955</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2021</rights><rights>This journal is © The Royal Society of Chemistry 2021 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c494t-bb69c1eb8729a0376701dee05f1e8cb3550105bc507783a96c77ef9529e6d1513</citedby><cites>FETCH-LOGICAL-c494t-bb69c1eb8729a0376701dee05f1e8cb3550105bc507783a96c77ef9529e6d1513</cites><orcidid>0000-0002-6465-7605</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698610/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698610/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35424045$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kareem, Rzgar Tawfeeq</creatorcontrib><creatorcontrib>Azizi, Bayan</creatorcontrib><creatorcontrib>Asnaashariisfahani, Manzarbanou</creatorcontrib><creatorcontrib>Ebadi, Abdolghaffar</creatorcontrib><creatorcontrib>Vessally, Esmail</creatorcontrib><title>Vicinal halo-trifluoromethylation of alkenes</title><title>RSC advances</title><addtitle>RSC Adv</addtitle><description>Both trifluoromethyl and halide groups are widely found in medicinally and pharmaceutically important compounds and, moreover, organohalides are commonly used as versatile intermediates in synthetic organic chemistry. Due to their prevalence and easy accessibility, alkene halo-trifluoromethylation provides a convenient way to install these valuable functionalities in complex targets. In this review, we summarize recent advances and achievements in this fast-growing research field. For clarity, the reactions were classified according to the type of halogen atom. Both trifluoromethyl and halide groups are widely found in medicinally and pharmaceutically important compounds and, moreover, organohalides are commonly used as versatile intermediates in synthetic organic chemistry.</description><subject>Alkenes</subject><subject>Chemistry</subject><subject>Organic chemistry</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdkc1LAzEQxYMottRevCsFLyKuTrJJdnMRSv0EQRD1GrJp1m5NNzXZFfrfG22t1bnMwPsxPN5DaB_DGYZUnI_BK-B5RtQW6hKgPCHAxfbG3UH9EKYQhzNMON5FnZRRQoGyLjp9qXRVKzuYKOuSxlelbZ13M9NMFlY1lasHrhwo-2ZqE_bQTqlsMP3V7qHn66un0W1y_3BzNxreJ5oK2iRFwYXGpoimhII04xngsTHASmxyXaSMAQZWaAZZlqdKcJ1lphSMCMPHmOG0hy6Wf-dtMTNjberGKyvnvpopv5BOVfKvUlcT-eo-ZM5FzmMsPXS8euDde2tCI2dV0MZaVRvXBkliEjzPKWURPfqHTl3rYyKRYoQSYJDSSJ0sKe1dCN6UazMY5FcP8hIeh989DCN8uGl_jf6kHoGDJeCDXqu_RaafJwWLeg</recordid><startdate>20210421</startdate><enddate>20210421</enddate><creator>Kareem, Rzgar Tawfeeq</creator><creator>Azizi, Bayan</creator><creator>Asnaashariisfahani, Manzarbanou</creator><creator>Ebadi, Abdolghaffar</creator><creator>Vessally, Esmail</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6465-7605</orcidid></search><sort><creationdate>20210421</creationdate><title>Vicinal halo-trifluoromethylation of alkenes</title><author>Kareem, Rzgar Tawfeeq ; Azizi, Bayan ; Asnaashariisfahani, Manzarbanou ; Ebadi, Abdolghaffar ; Vessally, Esmail</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-bb69c1eb8729a0376701dee05f1e8cb3550105bc507783a96c77ef9529e6d1513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alkenes</topic><topic>Chemistry</topic><topic>Organic chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kareem, Rzgar Tawfeeq</creatorcontrib><creatorcontrib>Azizi, Bayan</creatorcontrib><creatorcontrib>Asnaashariisfahani, Manzarbanou</creatorcontrib><creatorcontrib>Ebadi, Abdolghaffar</creatorcontrib><creatorcontrib>Vessally, Esmail</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kareem, Rzgar Tawfeeq</au><au>Azizi, Bayan</au><au>Asnaashariisfahani, Manzarbanou</au><au>Ebadi, Abdolghaffar</au><au>Vessally, Esmail</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vicinal halo-trifluoromethylation of alkenes</atitle><jtitle>RSC advances</jtitle><addtitle>RSC Adv</addtitle><date>2021-04-21</date><risdate>2021</risdate><volume>11</volume><issue>25</issue><spage>14941</spage><epage>14955</epage><pages>14941-14955</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>Both trifluoromethyl and halide groups are widely found in medicinally and pharmaceutically important compounds and, moreover, organohalides are commonly used as versatile intermediates in synthetic organic chemistry. Due to their prevalence and easy accessibility, alkene halo-trifluoromethylation provides a convenient way to install these valuable functionalities in complex targets. In this review, we summarize recent advances and achievements in this fast-growing research field. For clarity, the reactions were classified according to the type of halogen atom. Both trifluoromethyl and halide groups are widely found in medicinally and pharmaceutically important compounds and, moreover, organohalides are commonly used as versatile intermediates in synthetic organic chemistry.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>35424045</pmid><doi>10.1039/d0ra06872a</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-6465-7605</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2046-2069
ispartof RSC advances, 2021-04, Vol.11 (25), p.14941-14955
issn 2046-2069
2046-2069
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8698610
source PubMed Central
subjects Alkenes
Chemistry
Organic chemistry
title Vicinal halo-trifluoromethylation of alkenes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T11%3A39%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Vicinal%20halo-trifluoromethylation%20of%20alkenes&rft.jtitle=RSC%20advances&rft.au=Kareem,%20Rzgar%20Tawfeeq&rft.date=2021-04-21&rft.volume=11&rft.issue=25&rft.spage=14941&rft.epage=14955&rft.pages=14941-14955&rft.issn=2046-2069&rft.eissn=2046-2069&rft_id=info:doi/10.1039/d0ra06872a&rft_dat=%3Cproquest_pubme%3E2524205034%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c494t-bb69c1eb8729a0376701dee05f1e8cb3550105bc507783a96c77ef9529e6d1513%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2524205034&rft_id=info:pmid/35424045&rfr_iscdi=true