Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles
A new and efficient approach for the synthesis of oxygen and nitrogen heterocycles by organoselenium catalysis has been developed. The exo-cyclization proceeded smoothly under mild conditions with good functional group tolerance and excellent regioselectivity. Mechanistic studies revealed that 1-flu...
Gespeichert in:
Veröffentlicht in: | Organic letters 2016-02, Vol.18 (3), p.504-507 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 507 |
---|---|
container_issue | 3 |
container_start_page | 504 |
container_title | Organic letters |
container_volume | 18 |
creator | Guo, Ruizhi Huang, Jiachen Huang, Haiyan Zhao, Xiaodan |
description | A new and efficient approach for the synthesis of oxygen and nitrogen heterocycles by organoselenium catalysis has been developed. The exo-cyclization proceeded smoothly under mild conditions with good functional group tolerance and excellent regioselectivity. Mechanistic studies revealed that 1-fluoropyridinium triflate is key for oxidative cyclization. |
doi_str_mv | 10.1021/acs.orglett.5b03543 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1762965008</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1762965008</sourcerecordid><originalsourceid>FETCH-LOGICAL-a345t-7e4bd7ca89190c2ff62d3a705c70602ccda98543b6ca37e99a3dfcdf70e649953</originalsourceid><addsrcrecordid>eNp9kFtLwzAYhoMobk5_gSC99KZbmvSwXEpRJwwHHq5Dmn6tHW0ykxSsv96UVS-9-g6873d4ELqO8DLCJFoJaZfa1C04t0wKTJOYnqB5lBAaZjghp395imfowto9xpHvsHM0I2nG4pgkc_SyM7VQ2kILqum7MBdOtMM3lMHroNwH2MYGugp2X0MNKgyEKoPnxhk9VrlWTjSqUXWwAQdGy0G2YC_RWSVaC1dTXKD3h_u3fBNud49P-d02FDROXJhBXJSZFGsWMSxJVaWkpMJfLseLiZSlYGv_U5FKQTNgTNCykmWVYUhjxhK6QLfHuQejP3uwjneNldC2QoHuLY-ylLA0wXjtpfQolUZba6DiB9N0wgw8wnyEyT1MPsHkE0zvupkW9EUH5Z_nl54XrI6C0b3XvVH-339H_gBpUYSk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1762965008</pqid></control><display><type>article</type><title>Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles</title><source>American Chemical Society Journals</source><creator>Guo, Ruizhi ; Huang, Jiachen ; Huang, Haiyan ; Zhao, Xiaodan</creator><creatorcontrib>Guo, Ruizhi ; Huang, Jiachen ; Huang, Haiyan ; Zhao, Xiaodan</creatorcontrib><description>A new and efficient approach for the synthesis of oxygen and nitrogen heterocycles by organoselenium catalysis has been developed. The exo-cyclization proceeded smoothly under mild conditions with good functional group tolerance and excellent regioselectivity. Mechanistic studies revealed that 1-fluoropyridinium triflate is key for oxidative cyclization.</description><identifier>ISSN: 1523-7060</identifier><identifier>EISSN: 1523-7052</identifier><identifier>DOI: 10.1021/acs.orglett.5b03543</identifier><identifier>PMID: 26794425</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Organic letters, 2016-02, Vol.18 (3), p.504-507</ispartof><rights>Copyright © 2016 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a345t-7e4bd7ca89190c2ff62d3a705c70602ccda98543b6ca37e99a3dfcdf70e649953</citedby><cites>FETCH-LOGICAL-a345t-7e4bd7ca89190c2ff62d3a705c70602ccda98543b6ca37e99a3dfcdf70e649953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b03543$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.orglett.5b03543$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26794425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guo, Ruizhi</creatorcontrib><creatorcontrib>Huang, Jiachen</creatorcontrib><creatorcontrib>Huang, Haiyan</creatorcontrib><creatorcontrib>Zhao, Xiaodan</creatorcontrib><title>Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles</title><title>Organic letters</title><addtitle>Org. Lett</addtitle><description>A new and efficient approach for the synthesis of oxygen and nitrogen heterocycles by organoselenium catalysis has been developed. The exo-cyclization proceeded smoothly under mild conditions with good functional group tolerance and excellent regioselectivity. Mechanistic studies revealed that 1-fluoropyridinium triflate is key for oxidative cyclization.</description><issn>1523-7060</issn><issn>1523-7052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kFtLwzAYhoMobk5_gSC99KZbmvSwXEpRJwwHHq5Dmn6tHW0ykxSsv96UVS-9-g6873d4ELqO8DLCJFoJaZfa1C04t0wKTJOYnqB5lBAaZjghp395imfowto9xpHvsHM0I2nG4pgkc_SyM7VQ2kILqum7MBdOtMM3lMHroNwH2MYGugp2X0MNKgyEKoPnxhk9VrlWTjSqUXWwAQdGy0G2YC_RWSVaC1dTXKD3h_u3fBNud49P-d02FDROXJhBXJSZFGsWMSxJVaWkpMJfLseLiZSlYGv_U5FKQTNgTNCykmWVYUhjxhK6QLfHuQejP3uwjneNldC2QoHuLY-ylLA0wXjtpfQolUZba6DiB9N0wgw8wnyEyT1MPsHkE0zvupkW9EUH5Z_nl54XrI6C0b3XvVH-339H_gBpUYSk</recordid><startdate>20160205</startdate><enddate>20160205</enddate><creator>Guo, Ruizhi</creator><creator>Huang, Jiachen</creator><creator>Huang, Haiyan</creator><creator>Zhao, Xiaodan</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160205</creationdate><title>Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles</title><author>Guo, Ruizhi ; Huang, Jiachen ; Huang, Haiyan ; Zhao, Xiaodan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a345t-7e4bd7ca89190c2ff62d3a705c70602ccda98543b6ca37e99a3dfcdf70e649953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guo, Ruizhi</creatorcontrib><creatorcontrib>Huang, Jiachen</creatorcontrib><creatorcontrib>Huang, Haiyan</creatorcontrib><creatorcontrib>Zhao, Xiaodan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Organic letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guo, Ruizhi</au><au>Huang, Jiachen</au><au>Huang, Haiyan</au><au>Zhao, Xiaodan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles</atitle><jtitle>Organic letters</jtitle><addtitle>Org. Lett</addtitle><date>2016-02-05</date><risdate>2016</risdate><volume>18</volume><issue>3</issue><spage>504</spage><epage>507</epage><pages>504-507</pages><issn>1523-7060</issn><eissn>1523-7052</eissn><abstract>A new and efficient approach for the synthesis of oxygen and nitrogen heterocycles by organoselenium catalysis has been developed. The exo-cyclization proceeded smoothly under mild conditions with good functional group tolerance and excellent regioselectivity. Mechanistic studies revealed that 1-fluoropyridinium triflate is key for oxidative cyclization.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>26794425</pmid><doi>10.1021/acs.orglett.5b03543</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1523-7060 |
ispartof | Organic letters, 2016-02, Vol.18 (3), p.504-507 |
issn | 1523-7060 1523-7052 |
language | eng |
recordid | cdi_proquest_miscellaneous_1762965008 |
source | American Chemical Society Journals |
title | Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T16%3A22%3A44IST&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=Organoselenium-Catalyzed%20Synthesis%20of%20Oxygen-%20and%20Nitrogen-Containing%20Heterocycles&rft.jtitle=Organic%20letters&rft.au=Guo,%20Ruizhi&rft.date=2016-02-05&rft.volume=18&rft.issue=3&rft.spage=504&rft.epage=507&rft.pages=504-507&rft.issn=1523-7060&rft.eissn=1523-7052&rft_id=info:doi/10.1021/acs.orglett.5b03543&rft_dat=%3Cproquest_cross%3E1762965008%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1762965008&rft_id=info:pmid/26794425&rfr_iscdi=true |