Loading…

Asymmetric Simmons-Smith Cyclopropanation Of α,β-Unsaturated Bornane-2,3-Diol Acetals

Reactionofselected α, β-unsaturated aldehydes with bornane-2-exo,3-cxo-diol has afforded a series of novel, chiral acetals which, on treatment with a Simmons-Smithreagent, undergo diastereoselective(46 - 70 %d.e.) cyclopropanatioa

Saved in:
Bibliographic Details
Published in:Synthetic communications 1999-06, Vol.29 (11), p.1889-1902
Main Authors: Kaye, Perry T., Molema, Warner E.
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-c344t-8ef1729753295845c50a40f69425ca6bd639ec74cd96b2b33987951b242606773
cites cdi_FETCH-LOGICAL-c344t-8ef1729753295845c50a40f69425ca6bd639ec74cd96b2b33987951b242606773
container_end_page 1902
container_issue 11
container_start_page 1889
container_title Synthetic communications
container_volume 29
creator Kaye, Perry T.
Molema, Warner E.
description Reactionofselected α, β-unsaturated aldehydes with bornane-2-exo,3-cxo-diol has afforded a series of novel, chiral acetals which, on treatment with a Simmons-Smithreagent, undergo diastereoselective(46 - 70 %d.e.) cyclopropanatioa
doi_str_mv 10.1080/00397919908086177
format article
fullrecord <record><control><sourceid>crossref_infor</sourceid><recordid>TN_cdi_informaworld_taylorfrancis_310_1080_00397919908086177</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1080_00397919908086177</sourcerecordid><originalsourceid>FETCH-LOGICAL-c344t-8ef1729753295845c50a40f69425ca6bd639ec74cd96b2b33987951b242606773</originalsourceid><addsrcrecordid>eNqFkMtKAzEYhYMoWKsP4G4eoNHcZjIBN7XWCxS6qMVlyGQyGJlJShLReSx9kD6TU-quoKvDzznfz-EAcInRFUYlukaICi6wEMNRFpjzIzDCOSWQMEqOwWjnwyGAT8FZjG8I4ZyXYgReprHvOpOC1dnKdp13Ea46m16zWa9bvwl-o5xK1rts2WTbr8n2G65dVOk9qGTq7NYHp5yBZELhnfVtNtUmqTaeg5NmEHPxq2Owvp8_zx7hYvnwNJsuoKaMJViaBnMi-NBU5CXLdY4UQ00hGMm1Kqq6oMJoznQtiopUlIqSixxXhJECFZzTMcD7vzr4GINp5CbYToVeYiR3y8iDZQbmZs9Y1_jQqQ8f2lom1bc-NEE5baOkf-H8X_yAkukz0R8hE3u3</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Asymmetric Simmons-Smith Cyclopropanation Of α,β-Unsaturated Bornane-2,3-Diol Acetals</title><source>Taylor and Francis Science and Technology Collection</source><creator>Kaye, Perry T. ; Molema, Warner E.</creator><creatorcontrib>Kaye, Perry T. ; Molema, Warner E.</creatorcontrib><description>Reactionofselected α, β-unsaturated aldehydes with bornane-2-exo,3-cxo-diol has afforded a series of novel, chiral acetals which, on treatment with a Simmons-Smithreagent, undergo diastereoselective(46 - 70 %d.e.) cyclopropanatioa</description><identifier>ISSN: 0039-7911</identifier><identifier>EISSN: 1532-2432</identifier><identifier>DOI: 10.1080/00397919908086177</identifier><language>eng</language><publisher>Taylor &amp; Francis Group</publisher><ispartof>Synthetic communications, 1999-06, Vol.29 (11), p.1889-1902</ispartof><rights>Copyright Taylor &amp; Francis Group, LLC 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c344t-8ef1729753295845c50a40f69425ca6bd639ec74cd96b2b33987951b242606773</citedby><cites>FETCH-LOGICAL-c344t-8ef1729753295845c50a40f69425ca6bd639ec74cd96b2b33987951b242606773</cites></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>Kaye, Perry T.</creatorcontrib><creatorcontrib>Molema, Warner E.</creatorcontrib><title>Asymmetric Simmons-Smith Cyclopropanation Of α,β-Unsaturated Bornane-2,3-Diol Acetals</title><title>Synthetic communications</title><description>Reactionofselected α, β-unsaturated aldehydes with bornane-2-exo,3-cxo-diol has afforded a series of novel, chiral acetals which, on treatment with a Simmons-Smithreagent, undergo diastereoselective(46 - 70 %d.e.) cyclopropanatioa</description><issn>0039-7911</issn><issn>1532-2432</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkMtKAzEYhYMoWKsP4G4eoNHcZjIBN7XWCxS6qMVlyGQyGJlJShLReSx9kD6TU-quoKvDzznfz-EAcInRFUYlukaICi6wEMNRFpjzIzDCOSWQMEqOwWjnwyGAT8FZjG8I4ZyXYgReprHvOpOC1dnKdp13Ea46m16zWa9bvwl-o5xK1rts2WTbr8n2G65dVOk9qGTq7NYHp5yBZELhnfVtNtUmqTaeg5NmEHPxq2Owvp8_zx7hYvnwNJsuoKaMJViaBnMi-NBU5CXLdY4UQ00hGMm1Kqq6oMJoznQtiopUlIqSixxXhJECFZzTMcD7vzr4GINp5CbYToVeYiR3y8iDZQbmZs9Y1_jQqQ8f2lom1bc-NEE5baOkf-H8X_yAkukz0R8hE3u3</recordid><startdate>19990601</startdate><enddate>19990601</enddate><creator>Kaye, Perry T.</creator><creator>Molema, Warner E.</creator><general>Taylor &amp; Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19990601</creationdate><title>Asymmetric Simmons-Smith Cyclopropanation Of α,β-Unsaturated Bornane-2,3-Diol Acetals</title><author>Kaye, Perry T. ; Molema, Warner E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-8ef1729753295845c50a40f69425ca6bd639ec74cd96b2b33987951b242606773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaye, Perry T.</creatorcontrib><creatorcontrib>Molema, Warner E.</creatorcontrib><collection>CrossRef</collection><jtitle>Synthetic communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaye, Perry T.</au><au>Molema, Warner E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Asymmetric Simmons-Smith Cyclopropanation Of α,β-Unsaturated Bornane-2,3-Diol Acetals</atitle><jtitle>Synthetic communications</jtitle><date>1999-06-01</date><risdate>1999</risdate><volume>29</volume><issue>11</issue><spage>1889</spage><epage>1902</epage><pages>1889-1902</pages><issn>0039-7911</issn><eissn>1532-2432</eissn><abstract>Reactionofselected α, β-unsaturated aldehydes with bornane-2-exo,3-cxo-diol has afforded a series of novel, chiral acetals which, on treatment with a Simmons-Smithreagent, undergo diastereoselective(46 - 70 %d.e.) cyclopropanatioa</abstract><pub>Taylor &amp; Francis Group</pub><doi>10.1080/00397919908086177</doi><tpages>14</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0039-7911
ispartof Synthetic communications, 1999-06, Vol.29 (11), p.1889-1902
issn 0039-7911
1532-2432
language eng
recordid cdi_informaworld_taylorfrancis_310_1080_00397919908086177
source Taylor and Francis Science and Technology Collection
title Asymmetric Simmons-Smith Cyclopropanation Of α,β-Unsaturated Bornane-2,3-Diol Acetals
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T14%3A50%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Asymmetric%20Simmons-Smith%20Cyclopropanation%20Of%20%CE%B1,%CE%B2-Unsaturated%20Bornane-2,3-Diol%20Acetals&rft.jtitle=Synthetic%20communications&rft.au=Kaye,%20Perry%20T.&rft.date=1999-06-01&rft.volume=29&rft.issue=11&rft.spage=1889&rft.epage=1902&rft.pages=1889-1902&rft.issn=0039-7911&rft.eissn=1532-2432&rft_id=info:doi/10.1080/00397919908086177&rft_dat=%3Ccrossref_infor%3E10_1080_00397919908086177%3C/crossref_infor%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c344t-8ef1729753295845c50a40f69425ca6bd639ec74cd96b2b33987951b242606773%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