Diaryl hypervalent bromines and chlorines: synthesis, structures and reactivities
In the field of modern organic chemistry, hypervalent compounds have become indispensable tools for synthetic chemists, finding widespread applications in both academic research and industrial settings. While iodine-based reagents have historically dominated this research field, recent focus has shi...
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Veröffentlicht in: | Chemical science (Cambridge) 2024-01, Vol.15 (5), p.1557-1569 |
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description | In the field of modern organic chemistry, hypervalent compounds have become indispensable tools for synthetic chemists, finding widespread applications in both academic research and industrial settings. While iodine-based reagents have historically dominated this research field, recent focus has shifted to the potent yet relatively unexplored chemistry of diaryl λ
3
-bromanes and -chloranes. Despite their unique reactivities, the progress in their development and application within organic synthesis has been hampered by the absence of straightforward, reliable, and widely applicable preparative methods. However, recent investigations have uncovered innovative approaches and novel reactivity patterns associated with these specialized compounds. These discoveries suggest that we have only begun to tap into their potential, implying that there is much more to be explored in this captivating area of chemistry.
Diaryl hypervalent bromines and chlorines emerge as a novel foundation for advancing organic chemistry. This article provides an overview of the synthetic methodology, structural variations, and the latest transformations unearthed in this context. |
doi_str_mv | 10.1039/d3sc05382b |
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3
-bromanes and -chloranes. Despite their unique reactivities, the progress in their development and application within organic synthesis has been hampered by the absence of straightforward, reliable, and widely applicable preparative methods. However, recent investigations have uncovered innovative approaches and novel reactivity patterns associated with these specialized compounds. These discoveries suggest that we have only begun to tap into their potential, implying that there is much more to be explored in this captivating area of chemistry.
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3
-bromanes and -chloranes. Despite their unique reactivities, the progress in their development and application within organic synthesis has been hampered by the absence of straightforward, reliable, and widely applicable preparative methods. However, recent investigations have uncovered innovative approaches and novel reactivity patterns associated with these specialized compounds. These discoveries suggest that we have only begun to tap into their potential, implying that there is much more to be explored in this captivating area of chemistry.
Diaryl hypervalent bromines and chlorines emerge as a novel foundation for advancing organic chemistry. This article provides an overview of the synthetic methodology, structural variations, and the latest transformations unearthed in this context.</description><subject>Bromine</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Iodine</subject><subject>Organic chemistry</subject><subject>Reactivity</subject><subject>Reagents</subject><issn>2041-6520</issn><issn>2041-6539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdkctLHEEQxhtJUDFevBsGcpHgmOrXPLyIWU0iCEHUc9NT051pmcfaPbOw_316s5vJoy_VRf3q4ys-Qk4oXFDg5aeaBwTJC1btkUMGgqaZ5OWb-c_ggByH8ALxcU4ly_fJAS943OXZIXm4cdqv26RZL41f6db0Y1L5oXO9CYnu6wSbdvCb7jIJ635sTHDhPAmjn3Cc_A7yRuPoVm50Jrwjb61ugzne1SPy_OX2afEtvf_-9W5xfZ-iYOWYypwhBYsWJZRYoK2tEKUVlTAFt1gZybAuaJVJC6IomJZSI8skcCOyitf8iFxtdZdT1Zkao3OvW7X0rosXqUE79e-kd436MawUhYKVwCAqnO0U_PA6mTCqzgU0bat7M0xBsZKVlOVZLiL64T_0ZZh8H-_bUAAyz4BF6uOWQj-E4I2d3VBQm7TUDX9c_Errc4Tf_-1_Rn9nE4HTLeADztM_cfOfbmebDA</recordid><startdate>20240131</startdate><enddate>20240131</enddate><creator>Lanzi, Matteo</creator><creator>Wencel-Delord, Joanna</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/0000-0002-7094-5443</orcidid></search><sort><creationdate>20240131</creationdate><title>Diaryl hypervalent bromines and chlorines: synthesis, structures and reactivities</title><author>Lanzi, Matteo ; Wencel-Delord, Joanna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c429t-572c10fcfc509c8cfdf449f4b4e83fcbe52cd81b65f04882a55ac26503e46b3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Bromine</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Iodine</topic><topic>Organic chemistry</topic><topic>Reactivity</topic><topic>Reagents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lanzi, Matteo</creatorcontrib><creatorcontrib>Wencel-Delord, Joanna</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>Chemical science (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lanzi, Matteo</au><au>Wencel-Delord, Joanna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diaryl hypervalent bromines and chlorines: synthesis, structures and reactivities</atitle><jtitle>Chemical science (Cambridge)</jtitle><addtitle>Chem Sci</addtitle><date>2024-01-31</date><risdate>2024</risdate><volume>15</volume><issue>5</issue><spage>1557</spage><epage>1569</epage><pages>1557-1569</pages><issn>2041-6520</issn><eissn>2041-6539</eissn><abstract>In the field of modern organic chemistry, hypervalent compounds have become indispensable tools for synthetic chemists, finding widespread applications in both academic research and industrial settings. While iodine-based reagents have historically dominated this research field, recent focus has shifted to the potent yet relatively unexplored chemistry of diaryl λ
3
-bromanes and -chloranes. Despite their unique reactivities, the progress in their development and application within organic synthesis has been hampered by the absence of straightforward, reliable, and widely applicable preparative methods. However, recent investigations have uncovered innovative approaches and novel reactivity patterns associated with these specialized compounds. These discoveries suggest that we have only begun to tap into their potential, implying that there is much more to be explored in this captivating area of chemistry.
Diaryl hypervalent bromines and chlorines emerge as a novel foundation for advancing organic chemistry. This article provides an overview of the synthetic methodology, structural variations, and the latest transformations unearthed in this context.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>38303936</pmid><doi>10.1039/d3sc05382b</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-7094-5443</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bromine Chemical synthesis Chemistry Iodine Organic chemistry Reactivity Reagents |
title | Diaryl hypervalent bromines and chlorines: synthesis, structures and reactivities |
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