Diastereoselective Gold(I)-Catalyzed [2+2+2] Cycloaddition of Oxo-1,5-enynes

Abstract The intramolecular gold(I)-catalyzed [2+2+2] cycloaddition of oxo-1,5-enynes bearing protected homopropargylic alcohols provides access to oxatricyclic adducts with good to excellent diastereoselectivity.

Saved in:
Bibliographic Details
Published in:Synthesis (Stuttgart) 2016-10, Vol.48 (19), p.3183-3198
Main Authors: Calleja, Pilar, Muratore, Michael E., Jiménez, Tania, Echavarren, Antonio M.
Format: Article
Language:English
Citations: 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-c317t-5e420b5c26b94120123ee65eb5280b662f391f856f5b5f5387bbc8427c1d713a3
cites
container_end_page 3198
container_issue 19
container_start_page 3183
container_title Synthesis (Stuttgart)
container_volume 48
creator Calleja, Pilar
Muratore, Michael E.
Jiménez, Tania
Echavarren, Antonio M.
description Abstract The intramolecular gold(I)-catalyzed [2+2+2] cycloaddition of oxo-1,5-enynes bearing protected homopropargylic alcohols provides access to oxatricyclic adducts with good to excellent diastereoselectivity.
doi_str_mv 10.1055/s-0035-1562452
format article
fullrecord <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1055_s_0035_1562452</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_s_0035_1562452</sourcerecordid><originalsourceid>FETCH-LOGICAL-c317t-5e420b5c26b94120123ee65eb5280b662f391f856f5b5f5387bbc8427c1d713a3</originalsourceid><addsrcrecordid>eNp1kE1Lw0AQhhdRsFavnnNUdOt-ZLLJUVKthUIvCoLIsruZxZQ0K9koxl9vSnuV9zCHd55heAi55GzGGcBdpIxJoBwykYI4IhOeSkUFZ6_HZDJWBVV5zk_JWYwbxpgSspiQ1bw2sccOQ8QGXV9_Y7IITXW1vKal6U0z_GKVvImbMe9JObgmmKqq-zq0SfDJ-idQfgsU26HFeE5OvGkiXhzmlLw8PjyXT3S1XizL-xV1kqueAqaCWXAis0XKBeNCImaAFkTObJYJLwvuc8g8WPAgc2Wty1OhHK8Ul0ZOyWx_13Uhxg69_uzqrekGzZneudBR71zog4sRoHug_6hxi3oTvrp2_PC__T_zIV1H</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Diastereoselective Gold(I)-Catalyzed [2+2+2] Cycloaddition of Oxo-1,5-enynes</title><source>Thieme Connect Journals</source><creator>Calleja, Pilar ; Muratore, Michael E. ; Jiménez, Tania ; Echavarren, Antonio M.</creator><creatorcontrib>Calleja, Pilar ; Muratore, Michael E. ; Jiménez, Tania ; Echavarren, Antonio M.</creatorcontrib><description>Abstract The intramolecular gold(I)-catalyzed [2+2+2] cycloaddition of oxo-1,5-enynes bearing protected homopropargylic alcohols provides access to oxatricyclic adducts with good to excellent diastereoselectivity.</description><identifier>ISSN: 0039-7881</identifier><identifier>EISSN: 1437-210X</identifier><identifier>DOI: 10.1055/s-0035-1562452</identifier><language>eng</language><publisher>Stuttgart · New York: Georg Thieme Verlag</publisher><ispartof>Synthesis (Stuttgart), 2016-10, Vol.48 (19), p.3183-3198</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c317t-5e420b5c26b94120123ee65eb5280b662f391f856f5b5f5387bbc8427c1d713a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0035-1562452.pdf$$EPDF$$P50$$Gthieme$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-0035-1562452$$EHTML$$P50$$Gthieme$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3017,3018,27924,27925,54559,54560</link.rule.ids></links><search><creatorcontrib>Calleja, Pilar</creatorcontrib><creatorcontrib>Muratore, Michael E.</creatorcontrib><creatorcontrib>Jiménez, Tania</creatorcontrib><creatorcontrib>Echavarren, Antonio M.</creatorcontrib><title>Diastereoselective Gold(I)-Catalyzed [2+2+2] Cycloaddition of Oxo-1,5-enynes</title><title>Synthesis (Stuttgart)</title><addtitle>Synthesis</addtitle><description>Abstract The intramolecular gold(I)-catalyzed [2+2+2] cycloaddition of oxo-1,5-enynes bearing protected homopropargylic alcohols provides access to oxatricyclic adducts with good to excellent diastereoselectivity.</description><issn>0039-7881</issn><issn>1437-210X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>0U6</sourceid><recordid>eNp1kE1Lw0AQhhdRsFavnnNUdOt-ZLLJUVKthUIvCoLIsruZxZQ0K9koxl9vSnuV9zCHd55heAi55GzGGcBdpIxJoBwykYI4IhOeSkUFZ6_HZDJWBVV5zk_JWYwbxpgSspiQ1bw2sccOQ8QGXV9_Y7IITXW1vKal6U0z_GKVvImbMe9JObgmmKqq-zq0SfDJ-idQfgsU26HFeE5OvGkiXhzmlLw8PjyXT3S1XizL-xV1kqueAqaCWXAis0XKBeNCImaAFkTObJYJLwvuc8g8WPAgc2Wty1OhHK8Ul0ZOyWx_13Uhxg69_uzqrekGzZneudBR71zog4sRoHug_6hxi3oTvrp2_PC__T_zIV1H</recordid><startdate>20161004</startdate><enddate>20161004</enddate><creator>Calleja, Pilar</creator><creator>Muratore, Michael E.</creator><creator>Jiménez, Tania</creator><creator>Echavarren, Antonio M.</creator><general>Georg Thieme Verlag</general><scope>0U6</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20161004</creationdate><title>Diastereoselective Gold(I)-Catalyzed [2+2+2] Cycloaddition of Oxo-1,5-enynes</title><author>Calleja, Pilar ; Muratore, Michael E. ; Jiménez, Tania ; Echavarren, Antonio M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c317t-5e420b5c26b94120123ee65eb5280b662f391f856f5b5f5387bbc8427c1d713a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Calleja, Pilar</creatorcontrib><creatorcontrib>Muratore, Michael E.</creatorcontrib><creatorcontrib>Jiménez, Tania</creatorcontrib><creatorcontrib>Echavarren, Antonio M.</creatorcontrib><collection>Thieme Connect Journals Open Access</collection><collection>CrossRef</collection><jtitle>Synthesis (Stuttgart)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Calleja, Pilar</au><au>Muratore, Michael E.</au><au>Jiménez, Tania</au><au>Echavarren, Antonio M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diastereoselective Gold(I)-Catalyzed [2+2+2] Cycloaddition of Oxo-1,5-enynes</atitle><jtitle>Synthesis (Stuttgart)</jtitle><addtitle>Synthesis</addtitle><date>2016-10-04</date><risdate>2016</risdate><volume>48</volume><issue>19</issue><spage>3183</spage><epage>3198</epage><pages>3183-3198</pages><issn>0039-7881</issn><eissn>1437-210X</eissn><abstract>Abstract The intramolecular gold(I)-catalyzed [2+2+2] cycloaddition of oxo-1,5-enynes bearing protected homopropargylic alcohols provides access to oxatricyclic adducts with good to excellent diastereoselectivity.</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag</pub><doi>10.1055/s-0035-1562452</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0039-7881
ispartof Synthesis (Stuttgart), 2016-10, Vol.48 (19), p.3183-3198
issn 0039-7881
1437-210X
language eng
recordid cdi_crossref_primary_10_1055_s_0035_1562452
source Thieme Connect Journals
title Diastereoselective Gold(I)-Catalyzed [2+2+2] Cycloaddition of Oxo-1,5-enynes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T23%3A12%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-thieme_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Diastereoselective%20Gold(I)-Catalyzed%20%5B2+2+2%5D%20Cycloaddition%20of%20Oxo-1,5-enynes&rft.jtitle=Synthesis%20(Stuttgart)&rft.au=Calleja,%20Pilar&rft.date=2016-10-04&rft.volume=48&rft.issue=19&rft.spage=3183&rft.epage=3198&rft.pages=3183-3198&rft.issn=0039-7881&rft.eissn=1437-210X&rft_id=info:doi/10.1055/s-0035-1562452&rft_dat=%3Cthieme_cross%3E10_1055_s_0035_1562452%3C/thieme_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c317t-5e420b5c26b94120123ee65eb5280b662f391f856f5b5f5387bbc8427c1d713a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true