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Design, Synthesis, and Organocatalytic Activity of N-Heterocyclic Carbenes Functionalized with Hydrogen-Bond Donors in Enantioselective Reactions of Homoenolates
A focused library of chiral imidazolinium salts functionalized with urea‐type hydrogen‐bond donor moieties has been prepared from the chiral pool. The corresponding N‐heterocyclic carbenes were evaluated as organocatalysts in three enantioselective reactions involving homoenolate intermediates gener...
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Published in: | European journal of organic chemistry 2013-12, Vol.2013 (36), p.8253-8264 |
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container_end_page | 8264 |
container_issue | 36 |
container_start_page | 8253 |
container_title | European journal of organic chemistry |
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creator | Nawaz, Faisal Zaghouani, Mehdi Bonne, Damien Chuzel, Olivier Rodriguez, Jean Coquerel, Yoann |
description | A focused library of chiral imidazolinium salts functionalized with urea‐type hydrogen‐bond donor moieties has been prepared from the chiral pool. The corresponding N‐heterocyclic carbenes were evaluated as organocatalysts in three enantioselective reactions involving homoenolate intermediates generated from enals. The catalysts proved competent in enantioselective cyclopentannulation and γ‐lactonization reactions, a premiere for imidazoline‐based NHCs. This work conveys some new ideas and knowledge on the concepts of bifunctional enantioselective organocatalysis applied to NHCs.
Chiral 1,3‐imidazolin‐2‐ylidene NHCs functionalized with urea‐type hydrogen‐bond donors have been evaluated as organocatalysts in enantioselective reactions of homoenolates. Some unprecedented levels of enantioselectivity have been obtained. |
doi_str_mv | 10.1002/ejoc.201301366 |
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Chiral 1,3‐imidazolin‐2‐ylidene NHCs functionalized with urea‐type hydrogen‐bond donors have been evaluated as organocatalysts in enantioselective reactions of homoenolates. Some unprecedented levels of enantioselectivity have been obtained.</description><identifier>ISSN: 1434-193X</identifier><identifier>EISSN: 1099-0690</identifier><identifier>DOI: 10.1002/ejoc.201301366</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Carbenes ; Chemical Sciences ; Enantioselectivity ; Hydrogen bonds ; Organic chemistry ; Organocatalysis ; Umpolung</subject><ispartof>European journal of organic chemistry, 2013-12, Vol.2013 (36), p.8253-8264</ispartof><rights>Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3896-e47d11149ed76f90900b2f521fedaa3bb58535287bcb23163f96f2ff5a5aa74e3</citedby><cites>FETCH-LOGICAL-c3896-e47d11149ed76f90900b2f521fedaa3bb58535287bcb23163f96f2ff5a5aa74e3</cites><orcidid>0000-0003-0646-006X ; 0000-0003-4479-4626 ; 0000-0002-5825-9790</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://hal.science/hal-00979187$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Nawaz, Faisal</creatorcontrib><creatorcontrib>Zaghouani, Mehdi</creatorcontrib><creatorcontrib>Bonne, Damien</creatorcontrib><creatorcontrib>Chuzel, Olivier</creatorcontrib><creatorcontrib>Rodriguez, Jean</creatorcontrib><creatorcontrib>Coquerel, Yoann</creatorcontrib><title>Design, Synthesis, and Organocatalytic Activity of N-Heterocyclic Carbenes Functionalized with Hydrogen-Bond Donors in Enantioselective Reactions of Homoenolates</title><title>European journal of organic chemistry</title><addtitle>Eur. J. Org. Chem</addtitle><description>A focused library of chiral imidazolinium salts functionalized with urea‐type hydrogen‐bond donor moieties has been prepared from the chiral pool. The corresponding N‐heterocyclic carbenes were evaluated as organocatalysts in three enantioselective reactions involving homoenolate intermediates generated from enals. The catalysts proved competent in enantioselective cyclopentannulation and γ‐lactonization reactions, a premiere for imidazoline‐based NHCs. This work conveys some new ideas and knowledge on the concepts of bifunctional enantioselective organocatalysis applied to NHCs.
Chiral 1,3‐imidazolin‐2‐ylidene NHCs functionalized with urea‐type hydrogen‐bond donors have been evaluated as organocatalysts in enantioselective reactions of homoenolates. Some unprecedented levels of enantioselectivity have been obtained.</description><subject>Carbenes</subject><subject>Chemical Sciences</subject><subject>Enantioselectivity</subject><subject>Hydrogen bonds</subject><subject>Organic chemistry</subject><subject>Organocatalysis</subject><subject>Umpolung</subject><issn>1434-193X</issn><issn>1099-0690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkUFv0zAUxyMEEmPjytkSJ6Sl2HHi1MeSdQ2oWiU2BDfLSZ5bl8wetrsRvs2-KQ5B1W6TLPnJ_v3-T_ZLkncEzwjG2UfY23aWYULjYuxFckIw5ylmHL-MdU7zlHD643Xyxvs9xpgzRk6SxwvwemvO0fVgwi7W_hxJ06GN20pjWxlkPwTdokUb9L0OA7IKXaU1BHC2Hdo-XlXSNWDAo8uDiZQ1std_oEMPOuxQPXTObsGkn2xMvbDGOo-0QUsjTWQ99DAmA_oK8p_sxw61vbVgbC8D-LPklZK9h7f_99Pk2-XypqrT9Wb1uVqs05bOOUshLztCSM6hK5nimGPcZKrIiIJOSto0xbygRTYvm7bJKGFUcaYypQpZSFnmQE-TD1PuTvbizulb6QZhpRb1Yi3Gs_hlJSfz8p5E9v3E3jn76wA-iL09uPhwL0heZjgjeU4jNZuo1lnvHahjLMFiHJkYRyaOI4sCn4QH3cPwDC2WXzbVUzedXO0D_D660v0UrKRlIb5frUR1Xd-sixyLFf0L_UusRg</recordid><startdate>201312</startdate><enddate>201312</enddate><creator>Nawaz, Faisal</creator><creator>Zaghouani, Mehdi</creator><creator>Bonne, Damien</creator><creator>Chuzel, Olivier</creator><creator>Rodriguez, Jean</creator><creator>Coquerel, Yoann</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><general>Wiley-VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-0646-006X</orcidid><orcidid>https://orcid.org/0000-0003-4479-4626</orcidid><orcidid>https://orcid.org/0000-0002-5825-9790</orcidid></search><sort><creationdate>201312</creationdate><title>Design, Synthesis, and Organocatalytic Activity of N-Heterocyclic Carbenes Functionalized with Hydrogen-Bond Donors in Enantioselective Reactions of Homoenolates</title><author>Nawaz, Faisal ; Zaghouani, Mehdi ; Bonne, Damien ; Chuzel, Olivier ; Rodriguez, Jean ; Coquerel, Yoann</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3896-e47d11149ed76f90900b2f521fedaa3bb58535287bcb23163f96f2ff5a5aa74e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Carbenes</topic><topic>Chemical Sciences</topic><topic>Enantioselectivity</topic><topic>Hydrogen bonds</topic><topic>Organic chemistry</topic><topic>Organocatalysis</topic><topic>Umpolung</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nawaz, Faisal</creatorcontrib><creatorcontrib>Zaghouani, Mehdi</creatorcontrib><creatorcontrib>Bonne, Damien</creatorcontrib><creatorcontrib>Chuzel, Olivier</creatorcontrib><creatorcontrib>Rodriguez, Jean</creatorcontrib><creatorcontrib>Coquerel, Yoann</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>European journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nawaz, Faisal</au><au>Zaghouani, Mehdi</au><au>Bonne, Damien</au><au>Chuzel, Olivier</au><au>Rodriguez, Jean</au><au>Coquerel, Yoann</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design, Synthesis, and Organocatalytic Activity of N-Heterocyclic Carbenes Functionalized with Hydrogen-Bond Donors in Enantioselective Reactions of Homoenolates</atitle><jtitle>European journal of organic chemistry</jtitle><addtitle>Eur. J. Org. Chem</addtitle><date>2013-12</date><risdate>2013</risdate><volume>2013</volume><issue>36</issue><spage>8253</spage><epage>8264</epage><pages>8253-8264</pages><issn>1434-193X</issn><eissn>1099-0690</eissn><abstract>A focused library of chiral imidazolinium salts functionalized with urea‐type hydrogen‐bond donor moieties has been prepared from the chiral pool. The corresponding N‐heterocyclic carbenes were evaluated as organocatalysts in three enantioselective reactions involving homoenolate intermediates generated from enals. The catalysts proved competent in enantioselective cyclopentannulation and γ‐lactonization reactions, a premiere for imidazoline‐based NHCs. This work conveys some new ideas and knowledge on the concepts of bifunctional enantioselective organocatalysis applied to NHCs.
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subjects | Carbenes Chemical Sciences Enantioselectivity Hydrogen bonds Organic chemistry Organocatalysis Umpolung |
title | Design, Synthesis, and Organocatalytic Activity of N-Heterocyclic Carbenes Functionalized with Hydrogen-Bond Donors in Enantioselective Reactions of Homoenolates |
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