First Halogen Dance Reaction on Oxazoles. Synthesis of 4,5-Disubstituted 2-Phenyloxazoles

Abstract The halogen dance reaction was investigated on the ­oxazole system for the first time. Various 5-substituted 4-bromo-2-phenyloxazole derivatives are accessible via this convenient methodology.

Saved in:
Bibliographic Details
Published in:Synlett 2005-06, Vol.2005 (9), p.1433-1434
Main Authors: Stanetty, Peter, Spina, Markus, Mihovilovic, Marko D.
Format: Article
Language:English
Subjects:
letter
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-c340t-1df1c4f92b560e2b4264c97810f4f536d2a86934cc54911e8de87344bf3745ae3
cites
container_end_page 1434
container_issue 9
container_start_page 1433
container_title Synlett
container_volume 2005
creator Stanetty, Peter
Spina, Markus
Mihovilovic, Marko D.
description Abstract The halogen dance reaction was investigated on the ­oxazole system for the first time. Various 5-substituted 4-bromo-2-phenyloxazole derivatives are accessible via this convenient methodology.
doi_str_mv 10.1055/s-2005-868523
format article
fullrecord <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1055_s_2005_868523</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_s_2005_868523</sourcerecordid><originalsourceid>FETCH-LOGICAL-c340t-1df1c4f92b560e2b4264c97810f4f536d2a86934cc54911e8de87344bf3745ae3</originalsourceid><addsrcrecordid>eNp1kE1LAzEQhoMoWKtH7_kBTc3nbnKU1lqhUPHj4GnJZic2ZbuRTQrWX--WehUGBoZnXl4ehG4ZnTKq1F0inFJFdKEVF2doxKQoh5MpztGIGlEQxZm8RFcpbSllUhs6Qh-L0KeMl7aNn9Dhue0c4BewLofY4WHW3_YntpCm-PXQ5Q2kkHD0WE4UmYe0r1MOeZ-hwZw8b6A7tPHv4RpdeNsmuPnbY_S-eHibLclq_fg0u18RJyTNhDWeOekNr1VBgdeSF9KZUjPqpVeiaLjVhRHSOSUNY6Ab0KWQsvailMqCGCNyynV9TKkHX331YWf7Q8VodfRSperopTp5GfjJic-bADuotnHfd0PBf_Bf4EBi9w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>First Halogen Dance Reaction on Oxazoles. Synthesis of 4,5-Disubstituted 2-Phenyloxazoles</title><source>Thieme Connect Journals</source><creator>Stanetty, Peter ; Spina, Markus ; Mihovilovic, Marko D.</creator><creatorcontrib>Stanetty, Peter ; Spina, Markus ; Mihovilovic, Marko D.</creatorcontrib><description>Abstract The halogen dance reaction was investigated on the ­oxazole system for the first time. Various 5-substituted 4-bromo-2-phenyloxazole derivatives are accessible via this convenient methodology.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-2005-868523</identifier><language>eng</language><subject>letter</subject><ispartof>Synlett, 2005-06, Vol.2005 (9), p.1433-1434</ispartof><rights>Georg Thieme Verlag Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-1df1c4f92b560e2b4264c97810f4f536d2a86934cc54911e8de87344bf3745ae3</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-2005-868523.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2005-868523$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3004,3005,27901,27902,54534,54535</link.rule.ids></links><search><creatorcontrib>Stanetty, Peter</creatorcontrib><creatorcontrib>Spina, Markus</creatorcontrib><creatorcontrib>Mihovilovic, Marko D.</creatorcontrib><title>First Halogen Dance Reaction on Oxazoles. Synthesis of 4,5-Disubstituted 2-Phenyloxazoles</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract The halogen dance reaction was investigated on the ­oxazole system for the first time. Various 5-substituted 4-bromo-2-phenyloxazole derivatives are accessible via this convenient methodology.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LAzEQhoMoWKtH7_kBTc3nbnKU1lqhUPHj4GnJZic2ZbuRTQrWX--WehUGBoZnXl4ehG4ZnTKq1F0inFJFdKEVF2doxKQoh5MpztGIGlEQxZm8RFcpbSllUhs6Qh-L0KeMl7aNn9Dhue0c4BewLofY4WHW3_YntpCm-PXQ5Q2kkHD0WE4UmYe0r1MOeZ-hwZw8b6A7tPHv4RpdeNsmuPnbY_S-eHibLclq_fg0u18RJyTNhDWeOekNr1VBgdeSF9KZUjPqpVeiaLjVhRHSOSUNY6Ab0KWQsvailMqCGCNyynV9TKkHX331YWf7Q8VodfRSperopTp5GfjJic-bADuotnHfd0PBf_Bf4EBi9w</recordid><startdate>20050601</startdate><enddate>20050601</enddate><creator>Stanetty, Peter</creator><creator>Spina, Markus</creator><creator>Mihovilovic, Marko D.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20050601</creationdate><title>First Halogen Dance Reaction on Oxazoles. Synthesis of 4,5-Disubstituted 2-Phenyloxazoles</title><author>Stanetty, Peter ; Spina, Markus ; Mihovilovic, Marko D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-1df1c4f92b560e2b4264c97810f4f536d2a86934cc54911e8de87344bf3745ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stanetty, Peter</creatorcontrib><creatorcontrib>Spina, Markus</creatorcontrib><creatorcontrib>Mihovilovic, Marko D.</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stanetty, Peter</au><au>Spina, Markus</au><au>Mihovilovic, Marko D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>First Halogen Dance Reaction on Oxazoles. Synthesis of 4,5-Disubstituted 2-Phenyloxazoles</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2005-06-01</date><risdate>2005</risdate><volume>2005</volume><issue>9</issue><spage>1433</spage><epage>1434</epage><pages>1433-1434</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract The halogen dance reaction was investigated on the ­oxazole system for the first time. Various 5-substituted 4-bromo-2-phenyloxazole derivatives are accessible via this convenient methodology.</abstract><doi>10.1055/s-2005-868523</doi><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0936-5214
ispartof Synlett, 2005-06, Vol.2005 (9), p.1433-1434
issn 0936-5214
1437-2096
language eng
recordid cdi_crossref_primary_10_1055_s_2005_868523
source Thieme Connect Journals
subjects letter
title First Halogen Dance Reaction on Oxazoles. Synthesis of 4,5-Disubstituted 2-Phenyloxazoles
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T00%3A46%3A32IST&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=First%20Halogen%20Dance%20Reaction%20on%20Oxazoles.%20Synthesis%20of%204,5-Disubstituted%202-Phenyloxazoles&rft.jtitle=Synlett&rft.au=Stanetty,%20Peter&rft.date=2005-06-01&rft.volume=2005&rft.issue=9&rft.spage=1433&rft.epage=1434&rft.pages=1433-1434&rft.issn=0936-5214&rft.eissn=1437-2096&rft_id=info:doi/10.1055/s-2005-868523&rft_dat=%3Cthieme_cross%3E10_1055_s_2005_868523%3C/thieme_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c340t-1df1c4f92b560e2b4264c97810f4f536d2a86934cc54911e8de87344bf3745ae3%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