ChemInform Abstract: Enhanced Diastereoselectivity in the Asymmetric Ugi Reaction Using a New "Convertible" Isonitrile

ChemInform Abstract: Enhanced Diastereoselectivity in the Asymmetric Ugi Reaction Using a New "Convertible" Isonitrile

ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option....

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ChemInform 1999-07, Vol.30 (28), p.no-no
Hauptverfasser: Linderman, Russell J., Binet, Sophie, Petrich, Samantha R.
Format: Artikel
Sprache:eng
Schlagworte:
amino acids
amino acids, peptides
aminocarboxylic acids (hydrazinocarboxylic acids) and esters (benzene compounds)
optical resolution
peptides
stereochemistry (general
stereochemistry (general, optical resolution)
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page no
container_issue 28
container_start_page no
container_title ChemInform
container_volume 30
creator Linderman, Russell J.
Binet, Sophie
Petrich, Samantha R.
description ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
doi_str_mv 10.1002/chin.199928226
format Article
fullrecord <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_chin_199928226</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CHIN199928226</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1276-60b6a026bb91955489a3717c6f28a0cce91387b08d948b900ba22d1cede6d5f73</originalsourceid><addsrcrecordid>eNqF0M1LwzAYBvAgCs7p1XPYvTNJ16TxNqr7kDFBHDuGNH27RtdUkrK5_96OyfDm6b08v5eHB6F7SoaUEPZgKuuGVErJUsb4BerRhLGIcS4uUY_ImEYikeIa3YTw0eVjkbIe2mUV1HNXNr7G4zy0Xpv2ET-7SjsDBX6yOrTgoQmwBdPanW0P2DrcVoDH4VDX0Hpr8Gpj8Rt01DYOr4J1G6zxEvZ4kDVuB761-RYGeB4aZzuwhVt0VeptgLvf20eryfN7NosWr9N5Nl5EhjLBI05yrgnjeS6pTJJRKnUsqDC8ZKkmxoCkcSpykhZylOaSkFwzVtCuOfAiKUXcR8PTX-ObEDyU6svbWvuDokQdV1PH1dR5tQ7IE9h3LQ__pFU2my__2uhkbbfZ99lq_6m4iEWi1supkuvlJFtMX9Q0_gHjjIIs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>ChemInform Abstract: Enhanced Diastereoselectivity in the Asymmetric Ugi Reaction Using a New "Convertible" Isonitrile</title><source>Wiley Online Library All Journals</source><creator>Linderman, Russell J. ; Binet, Sophie ; Petrich, Samantha R.</creator><creatorcontrib>Linderman, Russell J. ; Binet, Sophie ; Petrich, Samantha R.</creatorcontrib><description>ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</description><identifier>ISSN: 0931-7597</identifier><identifier>EISSN: 1522-2667</identifier><identifier>DOI: 10.1002/chin.199928226</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>amino acids ; amino acids, peptides ; aminocarboxylic acids (hydrazinocarboxylic acids) and esters (benzene compounds) ; optical resolution ; peptides ; stereochemistry (general ; stereochemistry (general, optical resolution)</subject><ispartof>ChemInform, 1999-07, Vol.30 (28), p.no-no</ispartof><rights>Copyright © 1999 WILEY‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1276-60b6a026bb91955489a3717c6f28a0cce91387b08d948b900ba22d1cede6d5f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchin.199928226$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchin.199928226$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids></links><search><creatorcontrib>Linderman, Russell J.</creatorcontrib><creatorcontrib>Binet, Sophie</creatorcontrib><creatorcontrib>Petrich, Samantha R.</creatorcontrib><title>ChemInform Abstract: Enhanced Diastereoselectivity in the Asymmetric Ugi Reaction Using a New "Convertible" Isonitrile</title><title>ChemInform</title><addtitle>ChemInform</addtitle><description>ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</description><subject>amino acids</subject><subject>amino acids, peptides</subject><subject>aminocarboxylic acids (hydrazinocarboxylic acids) and esters (benzene compounds)</subject><subject>optical resolution</subject><subject>peptides</subject><subject>stereochemistry (general</subject><subject>stereochemistry (general, optical resolution)</subject><issn>0931-7597</issn><issn>1522-2667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqF0M1LwzAYBvAgCs7p1XPYvTNJ16TxNqr7kDFBHDuGNH27RtdUkrK5_96OyfDm6b08v5eHB6F7SoaUEPZgKuuGVErJUsb4BerRhLGIcS4uUY_ImEYikeIa3YTw0eVjkbIe2mUV1HNXNr7G4zy0Xpv2ET-7SjsDBX6yOrTgoQmwBdPanW0P2DrcVoDH4VDX0Hpr8Gpj8Rt01DYOr4J1G6zxEvZ4kDVuB761-RYGeB4aZzuwhVt0VeptgLvf20eryfN7NosWr9N5Nl5EhjLBI05yrgnjeS6pTJJRKnUsqDC8ZKkmxoCkcSpykhZylOaSkFwzVtCuOfAiKUXcR8PTX-ObEDyU6svbWvuDokQdV1PH1dR5tQ7IE9h3LQ__pFU2my__2uhkbbfZ99lq_6m4iEWi1supkuvlJFtMX9Q0_gHjjIIs</recordid><startdate>19990713</startdate><enddate>19990713</enddate><creator>Linderman, Russell J.</creator><creator>Binet, Sophie</creator><creator>Petrich, Samantha R.</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19990713</creationdate><title>ChemInform Abstract: Enhanced Diastereoselectivity in the Asymmetric Ugi Reaction Using a New "Convertible" Isonitrile</title><author>Linderman, Russell J. ; Binet, Sophie ; Petrich, Samantha R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1276-60b6a026bb91955489a3717c6f28a0cce91387b08d948b900ba22d1cede6d5f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>amino acids</topic><topic>amino acids, peptides</topic><topic>aminocarboxylic acids (hydrazinocarboxylic acids) and esters (benzene compounds)</topic><topic>optical resolution</topic><topic>peptides</topic><topic>stereochemistry (general</topic><topic>stereochemistry (general, optical resolution)</topic><toplevel>online_resources</toplevel><creatorcontrib>Linderman, Russell J.</creatorcontrib><creatorcontrib>Binet, Sophie</creatorcontrib><creatorcontrib>Petrich, Samantha R.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>ChemInform</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Linderman, Russell J.</au><au>Binet, Sophie</au><au>Petrich, Samantha R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ChemInform Abstract: Enhanced Diastereoselectivity in the Asymmetric Ugi Reaction Using a New "Convertible" Isonitrile</atitle><jtitle>ChemInform</jtitle><addtitle>ChemInform</addtitle><date>1999-07-13</date><risdate>1999</risdate><volume>30</volume><issue>28</issue><spage>no</spage><epage>no</epage><pages>no-no</pages><issn>0931-7597</issn><eissn>1522-2667</eissn><abstract>ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/chin.199928226</doi><tpages>1</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0931-7597
ispartof ChemInform, 1999-07, Vol.30 (28), p.no-no
issn 0931-7597
1522-2667
language eng
recordid cdi_crossref_primary_10_1002_chin_199928226
source Wiley Online Library All Journals
subjects amino acids
amino acids, peptides
aminocarboxylic acids (hydrazinocarboxylic acids) and esters (benzene compounds)
optical resolution
peptides
stereochemistry (general
stereochemistry (general, optical resolution)
title ChemInform Abstract: Enhanced Diastereoselectivity in the Asymmetric Ugi Reaction Using a New "Convertible" Isonitrile
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T11%3A52%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=ChemInform%20Abstract:%20Enhanced%20Diastereoselectivity%20in%20the%20Asymmetric%20Ugi%20Reaction%20Using%20a%20New%20%22Convertible%22%20Isonitrile&rft.jtitle=ChemInform&rft.au=Linderman,%20Russell%20J.&rft.date=1999-07-13&rft.volume=30&rft.issue=28&rft.spage=no&rft.epage=no&rft.pages=no-no&rft.issn=0931-7597&rft.eissn=1522-2667&rft_id=info:doi/10.1002/chin.199928226&rft_dat=%3Cwiley_cross%3ECHIN199928226%3C/wiley_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true