Loading…

Cr3+-Mediated Addition of Arylzincs to Aldehydes

Addition of arylzincs to aldehydes was achieved by making use of the novel transmetallation of arylzincs into Cr3+ compounds. Various α-substituted benzyl alcohols or 3-substituted 1(3H)-isobenzofuranones, containing reactive functional groups, were synthesized in good yields. Me3SiCl exerted benefi...

Full description

Saved in:
Bibliographic Details
Published in:Chemistry letters 1996-12, Vol.25 (12), p.1069-1070
Main Authors: Ogawa, Yoshihiro, Mori, Mitsuo, Saiga, Akihiro, Takagi, Kentaro
Format: Article
Language:English
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-c353t-93f34d8b0141ed013a8c37ffc6cb7ce9eef75a5bb332d89a82942cc22ca4ffc23
cites cdi_FETCH-LOGICAL-c353t-93f34d8b0141ed013a8c37ffc6cb7ce9eef75a5bb332d89a82942cc22ca4ffc23
container_end_page 1070
container_issue 12
container_start_page 1069
container_title Chemistry letters
container_volume 25
creator Ogawa, Yoshihiro
Mori, Mitsuo
Saiga, Akihiro
Takagi, Kentaro
description Addition of arylzincs to aldehydes was achieved by making use of the novel transmetallation of arylzincs into Cr3+ compounds. Various α-substituted benzyl alcohols or 3-substituted 1(3H)-isobenzofuranones, containing reactive functional groups, were synthesized in good yields. Me3SiCl exerted beneficial effects on the reaction.
doi_str_mv 10.1246/cl.1996.1069
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1460870852</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3135094971</sourcerecordid><originalsourceid>FETCH-LOGICAL-c353t-93f34d8b0141ed013a8c37ffc6cb7ce9eef75a5bb332d89a82942cc22ca4ffc23</originalsourceid><addsrcrecordid>eNptkDtPwzAYRS0EEqWw8QMiMULC50cce4wqXlIRC8yW44fqKk2KnQ7h15OoHRiY7nLuvdJB6BZDgQnjj6YtsJS8wMDlGVpgykQOFS7P0QIo53kFhFyiq5S2ACAkJQsEq0jv83dngx6czWprwxD6Lut9Vsex_QmdSdnQZ3Vr3Wa0Ll2jC6_b5G5OuURfz0-fq9d8_fHytqrXuaElHXJJPWVWNIAZdhYw1cLQynvDTVMZJ53zVanLpqGUWCG1IJIRYwgxmk0UoUt0d9zdx_774NKgtv0hdtOlwoyDqECUM_VwpEzsU4rOq30MOx1HhUHNTpRp1exEzU4mXJ7wjdsFM431Jrhh3Oq97v4c_Nf9BVzuZoU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1460870852</pqid></control><display><type>article</type><title>Cr3+-Mediated Addition of Arylzincs to Aldehydes</title><source>Oxford Journals Online</source><creator>Ogawa, Yoshihiro ; Mori, Mitsuo ; Saiga, Akihiro ; Takagi, Kentaro</creator><creatorcontrib>Ogawa, Yoshihiro ; Mori, Mitsuo ; Saiga, Akihiro ; Takagi, Kentaro</creatorcontrib><description>Addition of arylzincs to aldehydes was achieved by making use of the novel transmetallation of arylzincs into Cr3+ compounds. Various α-substituted benzyl alcohols or 3-substituted 1(3H)-isobenzofuranones, containing reactive functional groups, were synthesized in good yields. Me3SiCl exerted beneficial effects on the reaction.</description><identifier>ISSN: 0366-7022</identifier><identifier>EISSN: 1348-0715</identifier><identifier>DOI: 10.1246/cl.1996.1069</identifier><language>eng</language><publisher>Tokyo: The Chemical Society of Japan</publisher><ispartof>Chemistry letters, 1996-12, Vol.25 (12), p.1069-1070</ispartof><rights>The Chemical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-93f34d8b0141ed013a8c37ffc6cb7ce9eef75a5bb332d89a82942cc22ca4ffc23</citedby><cites>FETCH-LOGICAL-c353t-93f34d8b0141ed013a8c37ffc6cb7ce9eef75a5bb332d89a82942cc22ca4ffc23</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></links><search><creatorcontrib>Ogawa, Yoshihiro</creatorcontrib><creatorcontrib>Mori, Mitsuo</creatorcontrib><creatorcontrib>Saiga, Akihiro</creatorcontrib><creatorcontrib>Takagi, Kentaro</creatorcontrib><title>Cr3+-Mediated Addition of Arylzincs to Aldehydes</title><title>Chemistry letters</title><addtitle>Chemistry Letters</addtitle><description>Addition of arylzincs to aldehydes was achieved by making use of the novel transmetallation of arylzincs into Cr3+ compounds. Various α-substituted benzyl alcohols or 3-substituted 1(3H)-isobenzofuranones, containing reactive functional groups, were synthesized in good yields. Me3SiCl exerted beneficial effects on the reaction.</description><issn>0366-7022</issn><issn>1348-0715</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNptkDtPwzAYRS0EEqWw8QMiMULC50cce4wqXlIRC8yW44fqKk2KnQ7h15OoHRiY7nLuvdJB6BZDgQnjj6YtsJS8wMDlGVpgykQOFS7P0QIo53kFhFyiq5S2ACAkJQsEq0jv83dngx6czWprwxD6Lut9Vsex_QmdSdnQZ3Vr3Wa0Ll2jC6_b5G5OuURfz0-fq9d8_fHytqrXuaElHXJJPWVWNIAZdhYw1cLQynvDTVMZJ53zVanLpqGUWCG1IJIRYwgxmk0UoUt0d9zdx_774NKgtv0hdtOlwoyDqECUM_VwpEzsU4rOq30MOx1HhUHNTpRp1exEzU4mXJ7wjdsFM431Jrhh3Oq97v4c_Nf9BVzuZoU</recordid><startdate>19961201</startdate><enddate>19961201</enddate><creator>Ogawa, Yoshihiro</creator><creator>Mori, Mitsuo</creator><creator>Saiga, Akihiro</creator><creator>Takagi, Kentaro</creator><general>The Chemical Society of Japan</general><general>Chemical Society of Japan</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>19961201</creationdate><title>Cr3+-Mediated Addition of Arylzincs to Aldehydes</title><author>Ogawa, Yoshihiro ; Mori, Mitsuo ; Saiga, Akihiro ; Takagi, Kentaro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-93f34d8b0141ed013a8c37ffc6cb7ce9eef75a5bb332d89a82942cc22ca4ffc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ogawa, Yoshihiro</creatorcontrib><creatorcontrib>Mori, Mitsuo</creatorcontrib><creatorcontrib>Saiga, Akihiro</creatorcontrib><creatorcontrib>Takagi, Kentaro</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ogawa, Yoshihiro</au><au>Mori, Mitsuo</au><au>Saiga, Akihiro</au><au>Takagi, Kentaro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cr3+-Mediated Addition of Arylzincs to Aldehydes</atitle><jtitle>Chemistry letters</jtitle><addtitle>Chemistry Letters</addtitle><date>1996-12-01</date><risdate>1996</risdate><volume>25</volume><issue>12</issue><spage>1069</spage><epage>1070</epage><pages>1069-1070</pages><issn>0366-7022</issn><eissn>1348-0715</eissn><abstract>Addition of arylzincs to aldehydes was achieved by making use of the novel transmetallation of arylzincs into Cr3+ compounds. Various α-substituted benzyl alcohols or 3-substituted 1(3H)-isobenzofuranones, containing reactive functional groups, were synthesized in good yields. Me3SiCl exerted beneficial effects on the reaction.</abstract><cop>Tokyo</cop><pub>The Chemical Society of Japan</pub><doi>10.1246/cl.1996.1069</doi><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0366-7022
ispartof Chemistry letters, 1996-12, Vol.25 (12), p.1069-1070
issn 0366-7022
1348-0715
language eng
recordid cdi_proquest_journals_1460870852
source Oxford Journals Online
title Cr3+-Mediated Addition of Arylzincs to Aldehydes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T15%3A47%3A51IST&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=Cr3+-Mediated%20Addition%20of%20Arylzincs%20to%20Aldehydes&rft.jtitle=Chemistry%20letters&rft.au=Ogawa,%20Yoshihiro&rft.date=1996-12-01&rft.volume=25&rft.issue=12&rft.spage=1069&rft.epage=1070&rft.pages=1069-1070&rft.issn=0366-7022&rft.eissn=1348-0715&rft_id=info:doi/10.1246/cl.1996.1069&rft_dat=%3Cproquest_cross%3E3135094971%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c353t-93f34d8b0141ed013a8c37ffc6cb7ce9eef75a5bb332d89a82942cc22ca4ffc23%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1460870852&rft_id=info:pmid/&rfr_iscdi=true