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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...
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Published in: | RSC advances 2021-04, Vol.11 (25), p.14941-14955 |
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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 |
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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.
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language | eng |
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source | PubMed Central |
subjects | Alkenes Chemistry Organic chemistry |
title | Vicinal halo-trifluoromethylation of alkenes |
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