Direct use of allylic alcohols in the allylation of sulfonylimidates
We have developed catalytic allylation reactions of sulfonylimidates using allylic alcohols as allylating reagents. Stoichiometric amounts of neither activators nor bases are required in this reaction.
Gespeichert in:
Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2010-12, Vol.46 (45), p.8662-8664 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 8664 |
---|---|
container_issue | 45 |
container_start_page | 8662 |
container_title | Chemical communications (Cambridge, England) |
container_volume | 46 |
creator | Matsubara, Ryosuke Masuda, Koichiro Nakano, Jyunya Kobayashi, Shū |
description | We have developed catalytic allylation reactions of sulfonylimidates using allylic alcohols as allylating reagents. Stoichiometric amounts of neither activators nor bases are required in this reaction. |
doi_str_mv | 10.1039/c0cc03067h |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_763473818</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>763473818</sourcerecordid><originalsourceid>FETCH-LOGICAL-c352t-ae1ab0456ebde77f2436aa70ad7223ed7d1580bbbbbe1f4c0a6311c214d20c083</originalsourceid><addsrcrecordid>eNpFkEtLw0AUhQdRbK1u_AGSnSBE77zTpVhfUHCj4C5MZm7oyCRTM8mi_96EVj2bczl8HC6HkEsKtxT48s6CtcBB6c0RmVOuRC5F8Xk83XKZay7kjJyl9AWjqCxOyYzBUnJRqDlZrXyHts-GhFmsMxPCLng7uo2bGFLm26zf4D43vY_tRKUh1LEdwcY702M6Jye1CQkvDr4gH0-P7w8v-frt-fXhfp1bLlmfG6SmAiEVVg61rpngyhgNxmnGODrtxu-gmoS0FhaM4pRaRoVjYKHgC3K979128XvA1JeNTxZDMC3GIZVacaF5QSfyZk_aLqbUYV1uO9-YbldSKKfRyv_RRvjqUDtUDbo_9Hcl_gOPbWg_</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>763473818</pqid></control><display><type>article</type><title>Direct use of allylic alcohols in the allylation of sulfonylimidates</title><source>MEDLINE</source><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Matsubara, Ryosuke ; Masuda, Koichiro ; Nakano, Jyunya ; Kobayashi, Shū</creator><creatorcontrib>Matsubara, Ryosuke ; Masuda, Koichiro ; Nakano, Jyunya ; Kobayashi, Shū</creatorcontrib><description>We have developed catalytic allylation reactions of sulfonylimidates using allylic alcohols as allylating reagents. Stoichiometric amounts of neither activators nor bases are required in this reaction.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c0cc03067h</identifier><identifier>PMID: 20953486</identifier><language>eng</language><publisher>England</publisher><subject>Catalysis ; Esters ; Imidoesters - chemistry ; Propanols - chemistry</subject><ispartof>Chemical communications (Cambridge, England), 2010-12, Vol.46 (45), p.8662-8664</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-ae1ab0456ebde77f2436aa70ad7223ed7d1580bbbbbe1f4c0a6311c214d20c083</citedby><cites>FETCH-LOGICAL-c352t-ae1ab0456ebde77f2436aa70ad7223ed7d1580bbbbbe1f4c0a6311c214d20c083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27926,27927</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20953486$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsubara, Ryosuke</creatorcontrib><creatorcontrib>Masuda, Koichiro</creatorcontrib><creatorcontrib>Nakano, Jyunya</creatorcontrib><creatorcontrib>Kobayashi, Shū</creatorcontrib><title>Direct use of allylic alcohols in the allylation of sulfonylimidates</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>We have developed catalytic allylation reactions of sulfonylimidates using allylic alcohols as allylating reagents. Stoichiometric amounts of neither activators nor bases are required in this reaction.</description><subject>Catalysis</subject><subject>Esters</subject><subject>Imidoesters - chemistry</subject><subject>Propanols - chemistry</subject><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLw0AUhQdRbK1u_AGSnSBE77zTpVhfUHCj4C5MZm7oyCRTM8mi_96EVj2bczl8HC6HkEsKtxT48s6CtcBB6c0RmVOuRC5F8Xk83XKZay7kjJyl9AWjqCxOyYzBUnJRqDlZrXyHts-GhFmsMxPCLng7uo2bGFLm26zf4D43vY_tRKUh1LEdwcY702M6Jye1CQkvDr4gH0-P7w8v-frt-fXhfp1bLlmfG6SmAiEVVg61rpngyhgNxmnGODrtxu-gmoS0FhaM4pRaRoVjYKHgC3K979128XvA1JeNTxZDMC3GIZVacaF5QSfyZk_aLqbUYV1uO9-YbldSKKfRyv_RRvjqUDtUDbo_9Hcl_gOPbWg_</recordid><startdate>20101207</startdate><enddate>20101207</enddate><creator>Matsubara, Ryosuke</creator><creator>Masuda, Koichiro</creator><creator>Nakano, Jyunya</creator><creator>Kobayashi, Shū</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20101207</creationdate><title>Direct use of allylic alcohols in the allylation of sulfonylimidates</title><author>Matsubara, Ryosuke ; Masuda, Koichiro ; Nakano, Jyunya ; Kobayashi, Shū</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-ae1ab0456ebde77f2436aa70ad7223ed7d1580bbbbbe1f4c0a6311c214d20c083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Catalysis</topic><topic>Esters</topic><topic>Imidoesters - chemistry</topic><topic>Propanols - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsubara, Ryosuke</creatorcontrib><creatorcontrib>Masuda, Koichiro</creatorcontrib><creatorcontrib>Nakano, Jyunya</creatorcontrib><creatorcontrib>Kobayashi, Shū</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsubara, Ryosuke</au><au>Masuda, Koichiro</au><au>Nakano, Jyunya</au><au>Kobayashi, Shū</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct use of allylic alcohols in the allylation of sulfonylimidates</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2010-12-07</date><risdate>2010</risdate><volume>46</volume><issue>45</issue><spage>8662</spage><epage>8664</epage><pages>8662-8664</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>We have developed catalytic allylation reactions of sulfonylimidates using allylic alcohols as allylating reagents. Stoichiometric amounts of neither activators nor bases are required in this reaction.</abstract><cop>England</cop><pmid>20953486</pmid><doi>10.1039/c0cc03067h</doi><tpages>3</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1359-7345 |
ispartof | Chemical communications (Cambridge, England), 2010-12, Vol.46 (45), p.8662-8664 |
issn | 1359-7345 1364-548X |
language | eng |
recordid | cdi_proquest_miscellaneous_763473818 |
source | MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Catalysis Esters Imidoesters - chemistry Propanols - chemistry |
title | Direct use of allylic alcohols in the allylation of sulfonylimidates |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T06%3A14%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Direct%20use%20of%20allylic%20alcohols%20in%20the%20allylation%20of%20sulfonylimidates&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=Matsubara,%20Ryosuke&rft.date=2010-12-07&rft.volume=46&rft.issue=45&rft.spage=8662&rft.epage=8664&rft.pages=8662-8664&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/c0cc03067h&rft_dat=%3Cproquest_cross%3E763473818%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=763473818&rft_id=info:pmid/20953486&rfr_iscdi=true |