Loading…
A Ring-Closing Yne-Carbonyl Metathesis of Ynamides
An acid-catalyzed ring-closing ynamide-carbonyl metathesis is described here. This hetero RCM methodology is applicable to the construction of carbocycles as well as heterocycles such as chromenes, quinolizidines, indolizidines, and pyrrolizidines.
Saved in:
Published in: | Organic letters 2006-01, Vol.8 (2), p.231-234 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a282t-fbe331b2ab56a05bb50de182ec1bf8408a54bdb3dde380e1fd55cf77080bf3703 |
---|---|
cites | cdi_FETCH-LOGICAL-a282t-fbe331b2ab56a05bb50de182ec1bf8408a54bdb3dde380e1fd55cf77080bf3703 |
container_end_page | 234 |
container_issue | 2 |
container_start_page | 231 |
container_title | Organic letters |
container_volume | 8 |
creator | Kurtz, Kimberly C. M Hsung, Richard P Zhang, Yanshi |
description | An acid-catalyzed ring-closing ynamide-carbonyl metathesis is described here. This hetero RCM methodology is applicable to the construction of carbocycles as well as heterocycles such as chromenes, quinolizidines, indolizidines, and pyrrolizidines. |
doi_str_mv | 10.1021/ol052487s |
format | article |
fullrecord | <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_ol052487s</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>d20627310</sourcerecordid><originalsourceid>FETCH-LOGICAL-a282t-fbe331b2ab56a05bb50de182ec1bf8408a54bdb3dde380e1fd55cf77080bf3703</originalsourceid><addsrcrecordid>eNptjztPwzAUhS0EoqUw8AdQFgYGw7UdJ2asovKQipAQDEyRHV9DqjSu7HTov8coVVmYzn18OvceQi4Z3DLg7M53IHmuynhEpkxyQcvUHx_qAibkLMYVAEuT-1MyYUUOSik-JXyevbX9F606H5Nmnz3SSgfj-12XveCgh2-Mbcy8Syu9bi3Gc3LidBfxYq8z8vGweK-e6PL18bmaL6nmig_UGRSCGa6NLDRIYyRYZIpjw4xT6b6WubFGWItCATJnpWxcWYIC40QJYkZuRt8m-BgDunoT2rUOu5pB_Zu7PuRO7NXIbrZmjfaP3AdNwPUI6CbWK78NfXr9H6MfTf9eSA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A Ring-Closing Yne-Carbonyl Metathesis of Ynamides</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Kurtz, Kimberly C. M ; Hsung, Richard P ; Zhang, Yanshi</creator><creatorcontrib>Kurtz, Kimberly C. M ; Hsung, Richard P ; Zhang, Yanshi</creatorcontrib><description>An acid-catalyzed ring-closing ynamide-carbonyl metathesis is described here. This hetero RCM methodology is applicable to the construction of carbocycles as well as heterocycles such as chromenes, quinolizidines, indolizidines, and pyrrolizidines.</description><identifier>ISSN: 1523-7060</identifier><identifier>EISSN: 1523-7052</identifier><identifier>DOI: 10.1021/ol052487s</identifier><identifier>PMID: 16408882</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Amides - chemical synthesis ; Amides - chemistry ; Catalysis ; Cyclization ; Heterocyclic Compounds, 2-Ring - chemical synthesis ; Heterocyclic Compounds, 2-Ring - chemistry ; Molecular Structure ; Oxidation-Reduction ; Pyrrolizidine Alkaloids - chemical synthesis ; Pyrrolizidine Alkaloids - chemistry</subject><ispartof>Organic letters, 2006-01, Vol.8 (2), p.231-234</ispartof><rights>Copyright © 2006 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a282t-fbe331b2ab56a05bb50de182ec1bf8408a54bdb3dde380e1fd55cf77080bf3703</citedby><cites>FETCH-LOGICAL-a282t-fbe331b2ab56a05bb50de182ec1bf8408a54bdb3dde380e1fd55cf77080bf3703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16408882$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kurtz, Kimberly C. M</creatorcontrib><creatorcontrib>Hsung, Richard P</creatorcontrib><creatorcontrib>Zhang, Yanshi</creatorcontrib><title>A Ring-Closing Yne-Carbonyl Metathesis of Ynamides</title><title>Organic letters</title><addtitle>Org. Lett</addtitle><description>An acid-catalyzed ring-closing ynamide-carbonyl metathesis is described here. This hetero RCM methodology is applicable to the construction of carbocycles as well as heterocycles such as chromenes, quinolizidines, indolizidines, and pyrrolizidines.</description><subject>Amides - chemical synthesis</subject><subject>Amides - chemistry</subject><subject>Catalysis</subject><subject>Cyclization</subject><subject>Heterocyclic Compounds, 2-Ring - chemical synthesis</subject><subject>Heterocyclic Compounds, 2-Ring - chemistry</subject><subject>Molecular Structure</subject><subject>Oxidation-Reduction</subject><subject>Pyrrolizidine Alkaloids - chemical synthesis</subject><subject>Pyrrolizidine Alkaloids - chemistry</subject><issn>1523-7060</issn><issn>1523-7052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNptjztPwzAUhS0EoqUw8AdQFgYGw7UdJ2asovKQipAQDEyRHV9DqjSu7HTov8coVVmYzn18OvceQi4Z3DLg7M53IHmuynhEpkxyQcvUHx_qAibkLMYVAEuT-1MyYUUOSik-JXyevbX9F606H5Nmnz3SSgfj-12XveCgh2-Mbcy8Syu9bi3Gc3LidBfxYq8z8vGweK-e6PL18bmaL6nmig_UGRSCGa6NLDRIYyRYZIpjw4xT6b6WubFGWItCATJnpWxcWYIC40QJYkZuRt8m-BgDunoT2rUOu5pB_Zu7PuRO7NXIbrZmjfaP3AdNwPUI6CbWK78NfXr9H6MfTf9eSA</recordid><startdate>20060119</startdate><enddate>20060119</enddate><creator>Kurtz, Kimberly C. M</creator><creator>Hsung, Richard P</creator><creator>Zhang, Yanshi</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20060119</creationdate><title>A Ring-Closing Yne-Carbonyl Metathesis of Ynamides</title><author>Kurtz, Kimberly C. M ; Hsung, Richard P ; Zhang, Yanshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a282t-fbe331b2ab56a05bb50de182ec1bf8408a54bdb3dde380e1fd55cf77080bf3703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Amides - chemical synthesis</topic><topic>Amides - chemistry</topic><topic>Catalysis</topic><topic>Cyclization</topic><topic>Heterocyclic Compounds, 2-Ring - chemical synthesis</topic><topic>Heterocyclic Compounds, 2-Ring - chemistry</topic><topic>Molecular Structure</topic><topic>Oxidation-Reduction</topic><topic>Pyrrolizidine Alkaloids - chemical synthesis</topic><topic>Pyrrolizidine Alkaloids - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kurtz, Kimberly C. M</creatorcontrib><creatorcontrib>Hsung, Richard P</creatorcontrib><creatorcontrib>Zhang, Yanshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Organic letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kurtz, Kimberly C. M</au><au>Hsung, Richard P</au><au>Zhang, Yanshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Ring-Closing Yne-Carbonyl Metathesis of Ynamides</atitle><jtitle>Organic letters</jtitle><addtitle>Org. Lett</addtitle><date>2006-01-19</date><risdate>2006</risdate><volume>8</volume><issue>2</issue><spage>231</spage><epage>234</epage><pages>231-234</pages><issn>1523-7060</issn><eissn>1523-7052</eissn><abstract>An acid-catalyzed ring-closing ynamide-carbonyl metathesis is described here. This hetero RCM methodology is applicable to the construction of carbocycles as well as heterocycles such as chromenes, quinolizidines, indolizidines, and pyrrolizidines.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>16408882</pmid><doi>10.1021/ol052487s</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1523-7060 |
ispartof | Organic letters, 2006-01, Vol.8 (2), p.231-234 |
issn | 1523-7060 1523-7052 |
language | eng |
recordid | cdi_crossref_primary_10_1021_ol052487s |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Amides - chemical synthesis Amides - chemistry Catalysis Cyclization Heterocyclic Compounds, 2-Ring - chemical synthesis Heterocyclic Compounds, 2-Ring - chemistry Molecular Structure Oxidation-Reduction Pyrrolizidine Alkaloids - chemical synthesis Pyrrolizidine Alkaloids - chemistry |
title | A Ring-Closing Yne-Carbonyl Metathesis of Ynamides |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T09%3A30%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Ring-Closing%20Yne-Carbonyl%20Metathesis%20of%20Ynamides&rft.jtitle=Organic%20letters&rft.au=Kurtz,%20Kimberly%20C.%20M&rft.date=2006-01-19&rft.volume=8&rft.issue=2&rft.spage=231&rft.epage=234&rft.pages=231-234&rft.issn=1523-7060&rft.eissn=1523-7052&rft_id=info:doi/10.1021/ol052487s&rft_dat=%3Cacs_cross%3Ed20627310%3C/acs_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a282t-fbe331b2ab56a05bb50de182ec1bf8408a54bdb3dde380e1fd55cf77080bf3703%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/16408882&rfr_iscdi=true |