ChemInform Abstract: Construction of an All-Carbon Quaternary Stereocenter by Organocatalytic Enantioselective [alpha]-Functionalization of [alpha]-Substituted [beta]-Ketocarbonyls with Electron Deficient Vinylarenes

The enantioselective reaction of ketones (II) and (VI) with vinylarenes (I) gives rise to desired dicarbonyl compounds (III) and (VII), which are readily converted into chiral pyrazolones (V) and (VIII), respectively.

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ChemInform 2015-12, Vol.46 (48)
Hauptverfasser: Liu, Shizhou, Tong, Mengchao, Yu, Yang, Xie, Hexin, Li, Hao, Wang, Wei
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 48
container_start_page
container_title ChemInform
container_volume 46
creator Liu, Shizhou
Tong, Mengchao
Yu, Yang
Xie, Hexin
Li, Hao
Wang, Wei
description The enantioselective reaction of ketones (II) and (VI) with vinylarenes (I) gives rise to desired dicarbonyl compounds (III) and (VII), which are readily converted into chiral pyrazolones (V) and (VIII), respectively.
doi_str_mv 10.1002/chin.201548140
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_1732536747</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3863253821</sourcerecordid><originalsourceid>FETCH-proquest_journals_17325367473</originalsourceid><addsrcrecordid>eNqNj01LAzEQhoMoWD-ungOet26yu03rrawtigeRipciZTbOuilpUvOhrL_Un2Mq9u5pXuZ955kZQi5YPmR5zq9kp8yQ56wqx6zMD8iAVZxnfDQSh2SQTwqWiWoijsmJ9-uUL8SYD8h33eHmzrTWbei08cGBDNe0tibJKIOyhtqWgqFTrbMaXJMajxECOgOup4sk0Eo0qdKmpw_uDYyVEED3QUk6M2ASxKPGBPtAugS97eAlm0fzSwetvmC_Zm8uYrpEhRjwlS4bDKl1jyFhd-t77emnCh2d7ZguTd5gq6RKN9BnlWxwaNCfkaMWtMfzv3pKLuezp_o22zr7HtGH1drG9IT2KyYKXhUjUYrif6kfb8F6FQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1732536747</pqid></control><display><type>article</type><title>ChemInform Abstract: Construction of an All-Carbon Quaternary Stereocenter by Organocatalytic Enantioselective [alpha]-Functionalization of [alpha]-Substituted [beta]-Ketocarbonyls with Electron Deficient Vinylarenes</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Liu, Shizhou ; Tong, Mengchao ; Yu, Yang ; Xie, Hexin ; Li, Hao ; Wang, Wei</creator><creatorcontrib>Liu, Shizhou ; Tong, Mengchao ; Yu, Yang ; Xie, Hexin ; Li, Hao ; Wang, Wei</creatorcontrib><description>The enantioselective reaction of ketones (II) and (VI) with vinylarenes (I) gives rise to desired dicarbonyl compounds (III) and (VII), which are readily converted into chiral pyrazolones (V) and (VIII), respectively.</description><identifier>ISSN: 0931-7597</identifier><identifier>EISSN: 1522-2667</identifier><identifier>DOI: 10.1002/chin.201548140</identifier><language>eng</language><publisher>Frankfurt: Wiley Subscription Services, Inc</publisher><ispartof>ChemInform, 2015-12, Vol.46 (48)</ispartof><rights>2015 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Liu, Shizhou</creatorcontrib><creatorcontrib>Tong, Mengchao</creatorcontrib><creatorcontrib>Yu, Yang</creatorcontrib><creatorcontrib>Xie, Hexin</creatorcontrib><creatorcontrib>Li, Hao</creatorcontrib><creatorcontrib>Wang, Wei</creatorcontrib><title>ChemInform Abstract: Construction of an All-Carbon Quaternary Stereocenter by Organocatalytic Enantioselective [alpha]-Functionalization of [alpha]-Substituted [beta]-Ketocarbonyls with Electron Deficient Vinylarenes</title><title>ChemInform</title><description>The enantioselective reaction of ketones (II) and (VI) with vinylarenes (I) gives rise to desired dicarbonyl compounds (III) and (VII), which are readily converted into chiral pyrazolones (V) and (VIII), respectively.</description><issn>0931-7597</issn><issn>1522-2667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqNj01LAzEQhoMoWD-ungOet26yu03rrawtigeRipciZTbOuilpUvOhrL_Un2Mq9u5pXuZ955kZQi5YPmR5zq9kp8yQ56wqx6zMD8iAVZxnfDQSh2SQTwqWiWoijsmJ9-uUL8SYD8h33eHmzrTWbei08cGBDNe0tibJKIOyhtqWgqFTrbMaXJMajxECOgOup4sk0Eo0qdKmpw_uDYyVEED3QUk6M2ASxKPGBPtAugS97eAlm0fzSwetvmC_Zm8uYrpEhRjwlS4bDKl1jyFhd-t77emnCh2d7ZguTd5gq6RKN9BnlWxwaNCfkaMWtMfzv3pKLuezp_o22zr7HtGH1drG9IT2KyYKXhUjUYrif6kfb8F6FQ</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Liu, Shizhou</creator><creator>Tong, Mengchao</creator><creator>Yu, Yang</creator><creator>Xie, Hexin</creator><creator>Li, Hao</creator><creator>Wang, Wei</creator><general>Wiley Subscription Services, Inc</general><scope/></search><sort><creationdate>20151201</creationdate><title>ChemInform Abstract: Construction of an All-Carbon Quaternary Stereocenter by Organocatalytic Enantioselective [alpha]-Functionalization of [alpha]-Substituted [beta]-Ketocarbonyls with Electron Deficient Vinylarenes</title><author>Liu, Shizhou ; Tong, Mengchao ; Yu, Yang ; Xie, Hexin ; Li, Hao ; Wang, Wei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_17325367473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Liu, Shizhou</creatorcontrib><creatorcontrib>Tong, Mengchao</creatorcontrib><creatorcontrib>Yu, Yang</creatorcontrib><creatorcontrib>Xie, Hexin</creatorcontrib><creatorcontrib>Li, Hao</creatorcontrib><creatorcontrib>Wang, Wei</creatorcontrib><jtitle>ChemInform</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Shizhou</au><au>Tong, Mengchao</au><au>Yu, Yang</au><au>Xie, Hexin</au><au>Li, Hao</au><au>Wang, Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ChemInform Abstract: Construction of an All-Carbon Quaternary Stereocenter by Organocatalytic Enantioselective [alpha]-Functionalization of [alpha]-Substituted [beta]-Ketocarbonyls with Electron Deficient Vinylarenes</atitle><jtitle>ChemInform</jtitle><date>2015-12-01</date><risdate>2015</risdate><volume>46</volume><issue>48</issue><issn>0931-7597</issn><eissn>1522-2667</eissn><abstract>The enantioselective reaction of ketones (II) and (VI) with vinylarenes (I) gives rise to desired dicarbonyl compounds (III) and (VII), which are readily converted into chiral pyrazolones (V) and (VIII), respectively.</abstract><cop>Frankfurt</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/chin.201548140</doi></addata></record>
fulltext fulltext
identifier ISSN: 0931-7597
ispartof ChemInform, 2015-12, Vol.46 (48)
issn 0931-7597
1522-2667
language eng
recordid cdi_proquest_journals_1732536747
source Wiley Online Library Journals Frontfile Complete
title ChemInform Abstract: Construction of an All-Carbon Quaternary Stereocenter by Organocatalytic Enantioselective [alpha]-Functionalization of [alpha]-Substituted [beta]-Ketocarbonyls with Electron Deficient Vinylarenes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T11%3A02%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=ChemInform%20Abstract:%20Construction%20of%20an%20All-Carbon%20Quaternary%20Stereocenter%20by%20Organocatalytic%20Enantioselective%20%5Balpha%5D-Functionalization%20of%20%5Balpha%5D-Substituted%20%5Bbeta%5D-Ketocarbonyls%20with%20Electron%20Deficient%20Vinylarenes&rft.jtitle=ChemInform&rft.au=Liu,%20Shizhou&rft.date=2015-12-01&rft.volume=46&rft.issue=48&rft.issn=0931-7597&rft.eissn=1522-2667&rft_id=info:doi/10.1002/chin.201548140&rft_dat=%3Cproquest%3E3863253821%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1732536747&rft_id=info:pmid/&rfr_iscdi=true