Synthesis of 7-Formylindole Using the Bartoli Indole Methodology
Gespeichert in:
Veröffentlicht in: | Synlett 1992, Vol.1992 (1), p.79-80 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 80 |
---|---|
container_issue | 1 |
container_start_page | 79 |
container_title | Synlett |
container_volume | 1992 |
creator | Dobson, David R. Gilmore, Jeremy Long, David A. |
description | |
doi_str_mv | 10.1055/s-1992-21273 |
format | Article |
fullrecord | <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1055_s_1992_21273</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_s_1992_21273</sourcerecordid><originalsourceid>FETCH-LOGICAL-c366t-2fa27e2287f988989681b8b623fad4b967115bb132532ea2ae958cf83f0d5b6c3</originalsourceid><addsrcrecordid>eNptj7FOwzAURS0EEqWw8QEZ2MDgZ8eOvQEVhUpFDNDZclK7dZXGlR2G_H0TgpiY3pPuuVc6CF0DuQfC-UPCoBTFFGjBTtAEclZgSpQ4RROimMCcQn6OLlLaEQK5VGSCHj-7pt3a5FMWXFbgeYj7rvbNOtQ2WyXfbLI-zp5NbEPts8UYvNt2G_ovbLpLdOZMnezV752i1fzla_aGlx-vi9nTEldMiBZTZ2hhKZWFU1IqqYSEUpaCMmfWealEAcDLEhjljFpDjVVcVk4yR9a8FBWbortxt4ohpWidPkS_N7HTQPRgr5Me7PWPfY_fjPjBpMrULpqm8umvw4nKQQ3Y7Yi1W2_3Vu_Cd2x6jf9Hj1nTZnA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis of 7-Formylindole Using the Bartoli Indole Methodology</title><source>Thieme Connect Journals</source><creator>Dobson, David R. ; Gilmore, Jeremy ; Long, David A.</creator><creatorcontrib>Dobson, David R. ; Gilmore, Jeremy ; Long, David A.</creatorcontrib><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-1992-21273</identifier><language>eng</language><publisher>New york, NY: Thieme</publisher><subject>Chemistry ; Exact sciences and technology ; Heterocyclic compounds ; Heterocyclic compounds with only one n hetero atom and condensed derivatives ; letter ; Organic chemistry ; Preparations and properties</subject><ispartof>Synlett, 1992, Vol.1992 (1), p.79-80</ispartof><rights>Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c366t-2fa27e2287f988989681b8b623fad4b967115bb132532ea2ae958cf83f0d5b6c3</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-1992-21273.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><link.rule.ids>314,780,784,3017,3018,4024,27923,27924,27925,54559</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5094193$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Dobson, David R.</creatorcontrib><creatorcontrib>Gilmore, Jeremy</creatorcontrib><creatorcontrib>Long, David A.</creatorcontrib><title>Synthesis of 7-Formylindole Using the Bartoli Indole Methodology</title><title>Synlett</title><addtitle>Synlett</addtitle><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Heterocyclic compounds</subject><subject>Heterocyclic compounds with only one n hetero atom and condensed derivatives</subject><subject>letter</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNptj7FOwzAURS0EEqWw8QEZ2MDgZ8eOvQEVhUpFDNDZclK7dZXGlR2G_H0TgpiY3pPuuVc6CF0DuQfC-UPCoBTFFGjBTtAEclZgSpQ4RROimMCcQn6OLlLaEQK5VGSCHj-7pt3a5FMWXFbgeYj7rvbNOtQ2WyXfbLI-zp5NbEPts8UYvNt2G_ovbLpLdOZMnezV752i1fzla_aGlx-vi9nTEldMiBZTZ2hhKZWFU1IqqYSEUpaCMmfWealEAcDLEhjljFpDjVVcVk4yR9a8FBWbortxt4ohpWidPkS_N7HTQPRgr5Me7PWPfY_fjPjBpMrULpqm8umvw4nKQQ3Y7Yi1W2_3Vu_Cd2x6jf9Hj1nTZnA</recordid><startdate>1992</startdate><enddate>1992</enddate><creator>Dobson, David R.</creator><creator>Gilmore, Jeremy</creator><creator>Long, David A.</creator><general>Thieme</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>1992</creationdate><title>Synthesis of 7-Formylindole Using the Bartoli Indole Methodology</title><author>Dobson, David R. ; Gilmore, Jeremy ; Long, David A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c366t-2fa27e2287f988989681b8b623fad4b967115bb132532ea2ae958cf83f0d5b6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Heterocyclic compounds</topic><topic>Heterocyclic compounds with only one n hetero atom and condensed derivatives</topic><topic>letter</topic><topic>Organic chemistry</topic><topic>Preparations and properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dobson, David R.</creatorcontrib><creatorcontrib>Gilmore, Jeremy</creatorcontrib><creatorcontrib>Long, David A.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dobson, David R.</au><au>Gilmore, Jeremy</au><au>Long, David A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of 7-Formylindole Using the Bartoli Indole Methodology</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>1992</date><risdate>1992</risdate><volume>1992</volume><issue>1</issue><spage>79</spage><epage>80</epage><pages>79-80</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><cop>New york, NY</cop><cop>Stuttgart</cop><pub>Thieme</pub><doi>10.1055/s-1992-21273</doi><tpages>2</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0936-5214 |
ispartof | Synlett, 1992, Vol.1992 (1), p.79-80 |
issn | 0936-5214 1437-2096 |
language | eng |
recordid | cdi_crossref_primary_10_1055_s_1992_21273 |
source | Thieme Connect Journals |
subjects | Chemistry Exact sciences and technology Heterocyclic compounds Heterocyclic compounds with only one n hetero atom and condensed derivatives letter Organic chemistry Preparations and properties |
title | Synthesis of 7-Formylindole Using the Bartoli Indole Methodology |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T14%3A18%3A26IST&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=Synthesis%20of%207-Formylindole%20Using%20the%20Bartoli%20Indole%20Methodology&rft.jtitle=Synlett&rft.au=Dobson,%20David%20R.&rft.date=1992&rft.volume=1992&rft.issue=1&rft.spage=79&rft.epage=80&rft.pages=79-80&rft.issn=0936-5214&rft.eissn=1437-2096&rft_id=info:doi/10.1055/s-1992-21273&rft_dat=%3Cthieme_cross%3E10_1055_s_1992_21273%3C/thieme_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 |