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Copper(I)-catalyzed asymmetric 1,6-conjugate allylation
Catalytic asymmetric conjugate allylation of unsaturated carbonyl compounds is usually difficult to achieve, as 1,2-addition proceeds dominantly and high asymmetric induction is a challenging task. Herein, we disclose a copper(I)-NHC complex catalyzed asymmetric 1,6-conjugate allylation of 2,2-dimet...
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Published in: | Nature communications 2020-10, Vol.11 (1), p.5480-5480, Article 5480 |
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description | Catalytic asymmetric conjugate allylation of unsaturated carbonyl compounds is usually difficult to achieve, as 1,2-addition proceeds dominantly and high asymmetric induction is a challenging task. Herein, we disclose a copper(I)-NHC complex catalyzed asymmetric 1,6-conjugate allylation of 2,2-dimethyl-6-alkenyl-4
H
-1,3-dioxin-4-ones. The phenolic hydroxyl group in NHC ligands is found to be pivotal to obtain the desired products. Both aryl group and alkyl group at δ-position are well tolerated with the corresponding products generated in moderate to high yields and high enantioselectivity. Moreover, both 2-substituted and 3-substituted allylboronates serve as acceptable allylation reagents. At last, the synthetic utility of the products is demonstrated in several transformations by means of the versatile terminal olefin and dioxinone groups.
Catalytic asymmetric conjugate allylation of unsaturated carbonyl compounds is usually difficult to achieve due to competing 1,2-addition. Here, the authors report a copper(I)-catalyzed asymmetric 1,6-conjugate allylation of 2,2-dimethyl-6-alkenyl-4H-1,3-dioxin-4-ones with good scope and high enantioselectivity. |
doi_str_mv | 10.1038/s41467-020-19293-9 |
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H
-1,3-dioxin-4-ones. The phenolic hydroxyl group in NHC ligands is found to be pivotal to obtain the desired products. Both aryl group and alkyl group at δ-position are well tolerated with the corresponding products generated in moderate to high yields and high enantioselectivity. Moreover, both 2-substituted and 3-substituted allylboronates serve as acceptable allylation reagents. At last, the synthetic utility of the products is demonstrated in several transformations by means of the versatile terminal olefin and dioxinone groups.
Catalytic asymmetric conjugate allylation of unsaturated carbonyl compounds is usually difficult to achieve due to competing 1,2-addition. Here, the authors report a copper(I)-catalyzed asymmetric 1,6-conjugate allylation of 2,2-dimethyl-6-alkenyl-4H-1,3-dioxin-4-ones with good scope and high enantioselectivity.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/s41467-020-19293-9</identifier><identifier>PMID: 33127903</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>140/131 ; 140/58 ; 639/638/403/933 ; 639/638/77/883 ; 639/638/77/888 ; Allyl compounds ; Aromatic compounds ; Asymmetry ; Carbonyl compounds ; Carbonyls ; Chemical reactions ; Conjugates ; Coordination compounds ; Copper ; Dioxins ; Enantiomers ; Humanities and Social Sciences ; Hydroxyl groups ; multidisciplinary ; Phenolic compounds ; Phenols ; Reagents ; Science ; Science (multidisciplinary) ; Substitutes</subject><ispartof>Nature communications, 2020-10, Vol.11 (1), p.5480-5480, Article 5480</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c517t-884d2c775138bd1d84eff3f497f9cf45d3455eff61b699b1bfa7e3569a6a8ccd3</citedby><cites>FETCH-LOGICAL-c517t-884d2c775138bd1d84eff3f497f9cf45d3455eff61b699b1bfa7e3569a6a8ccd3</cites><orcidid>0000-0001-9604-5198 ; 0000-0002-5612-0664</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2471528439/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2471528439?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids></links><search><creatorcontrib>Shi, Chang-Yun</creatorcontrib><creatorcontrib>Pan, Zhi-Zhou</creatorcontrib><creatorcontrib>Tian, Ping</creatorcontrib><creatorcontrib>Yin, Liang</creatorcontrib><title>Copper(I)-catalyzed asymmetric 1,6-conjugate allylation</title><title>Nature communications</title><addtitle>Nat Commun</addtitle><description>Catalytic asymmetric conjugate allylation of unsaturated carbonyl compounds is usually difficult to achieve, as 1,2-addition proceeds dominantly and high asymmetric induction is a challenging task. Herein, we disclose a copper(I)-NHC complex catalyzed asymmetric 1,6-conjugate allylation of 2,2-dimethyl-6-alkenyl-4
H
-1,3-dioxin-4-ones. The phenolic hydroxyl group in NHC ligands is found to be pivotal to obtain the desired products. Both aryl group and alkyl group at δ-position are well tolerated with the corresponding products generated in moderate to high yields and high enantioselectivity. Moreover, both 2-substituted and 3-substituted allylboronates serve as acceptable allylation reagents. At last, the synthetic utility of the products is demonstrated in several transformations by means of the versatile terminal olefin and dioxinone groups.
Catalytic asymmetric conjugate allylation of unsaturated carbonyl compounds is usually difficult to achieve due to competing 1,2-addition. 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Zhi-Zhou</au><au>Tian, Ping</au><au>Yin, Liang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Copper(I)-catalyzed asymmetric 1,6-conjugate allylation</atitle><jtitle>Nature communications</jtitle><stitle>Nat Commun</stitle><date>2020-10-30</date><risdate>2020</risdate><volume>11</volume><issue>1</issue><spage>5480</spage><epage>5480</epage><pages>5480-5480</pages><artnum>5480</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>Catalytic asymmetric conjugate allylation of unsaturated carbonyl compounds is usually difficult to achieve, as 1,2-addition proceeds dominantly and high asymmetric induction is a challenging task. Herein, we disclose a copper(I)-NHC complex catalyzed asymmetric 1,6-conjugate allylation of 2,2-dimethyl-6-alkenyl-4
H
-1,3-dioxin-4-ones. The phenolic hydroxyl group in NHC ligands is found to be pivotal to obtain the desired products. Both aryl group and alkyl group at δ-position are well tolerated with the corresponding products generated in moderate to high yields and high enantioselectivity. Moreover, both 2-substituted and 3-substituted allylboronates serve as acceptable allylation reagents. At last, the synthetic utility of the products is demonstrated in several transformations by means of the versatile terminal olefin and dioxinone groups.
Catalytic asymmetric conjugate allylation of unsaturated carbonyl compounds is usually difficult to achieve due to competing 1,2-addition. Here, the authors report a copper(I)-catalyzed asymmetric 1,6-conjugate allylation of 2,2-dimethyl-6-alkenyl-4H-1,3-dioxin-4-ones with good scope and high enantioselectivity.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33127903</pmid><doi>10.1038/s41467-020-19293-9</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-9604-5198</orcidid><orcidid>https://orcid.org/0000-0002-5612-0664</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 140/131 140/58 639/638/403/933 639/638/77/883 639/638/77/888 Allyl compounds Aromatic compounds Asymmetry Carbonyl compounds Carbonyls Chemical reactions Conjugates Coordination compounds Copper Dioxins Enantiomers Humanities and Social Sciences Hydroxyl groups multidisciplinary Phenolic compounds Phenols Reagents Science Science (multidisciplinary) Substitutes |
title | Copper(I)-catalyzed asymmetric 1,6-conjugate allylation |
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