Ruthenium-catalyzed -alkylation of amino-1,3,5-triazines using alcohols

Ruthenium-catalyzed -alkylation of amino-1,3,5-triazines using alcohols

An efficient ruthenium-catalyzed N -alkylation of amino 1,3,5-triazines with alcohols was achieved via a BH/HA strategy. Following this simple, facile, and high atom economical protocol, a broad range of products was prepared in moderate to good yields and heterocyclic or benzylic alcohols containin...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:New journal of chemistry 2021-09, Vol.45 (35), p.15776-15779
Hauptverfasser: Zhao, Junna, Zhong, Pengzhen, Xie, Zhongpao, Zhou, Wei, Zhang, Chen, Cui, Dong-Mei
Format: Artikel
Sprache:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 15779
container_issue 35
container_start_page 15776
container_title New journal of chemistry
container_volume 45
creator Zhao, Junna
Zhong, Pengzhen
Xie, Zhongpao
Zhou, Wei
Zhang, Chen
Cui, Dong-Mei
description An efficient ruthenium-catalyzed N -alkylation of amino 1,3,5-triazines with alcohols was achieved via a BH/HA strategy. Following this simple, facile, and high atom economical protocol, a broad range of products was prepared in moderate to good yields and heterocyclic or benzylic alcohols containing various functionalities were tolerated. The application of the reaction is also further demonstrated by the synthesis of alkylated secondary amine-1,3,5-triazines from olefinated amino-1,3,5-triazines and alcohols via a one pot N -alkylation and reductive reactions. An efficient ruthenium-catalyzed N -alkylation of amino-1,3,5-triazines with alcohols was achieved via BH/HA strategy.
doi_str_mv 10.1039/d1nj03116c
format Article
fullrecord <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_d1nj03116c</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>d1nj03116c</sourcerecordid><originalsourceid>FETCH-rsc_primary_d1nj03116c3</originalsourceid><addsrcrecordid>eNqFjrsKwjAUQIMoWB-Lu5APMJpr2khn8TGLe7n0YVPTRJJ0aL9eB8HR6Rw4yyFkBXwLXKS7AkzDBYDMRyQCIVOW7iWMPw5xzHgSyymZed9wDnCQEJHLrQt1aVTXshwD6n4oC8pQP3uNQVlDbUWxVcYy2IhNwoJTOChTetp5ZR4UdW5rq_2CTCrUvlx-OSfr8-l-vDLn8-zlVIuuz3534l9_A3RfPS4</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Ruthenium-catalyzed -alkylation of amino-1,3,5-triazines using alcohols</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Zhao, Junna ; Zhong, Pengzhen ; Xie, Zhongpao ; Zhou, Wei ; Zhang, Chen ; Cui, Dong-Mei</creator><creatorcontrib>Zhao, Junna ; Zhong, Pengzhen ; Xie, Zhongpao ; Zhou, Wei ; Zhang, Chen ; Cui, Dong-Mei</creatorcontrib><description>An efficient ruthenium-catalyzed N -alkylation of amino 1,3,5-triazines with alcohols was achieved via a BH/HA strategy. Following this simple, facile, and high atom economical protocol, a broad range of products was prepared in moderate to good yields and heterocyclic or benzylic alcohols containing various functionalities were tolerated. The application of the reaction is also further demonstrated by the synthesis of alkylated secondary amine-1,3,5-triazines from olefinated amino-1,3,5-triazines and alcohols via a one pot N -alkylation and reductive reactions. An efficient ruthenium-catalyzed N -alkylation of amino-1,3,5-triazines with alcohols was achieved via BH/HA strategy.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/d1nj03116c</identifier><ispartof>New journal of chemistry, 2021-09, Vol.45 (35), p.15776-15779</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Zhao, Junna</creatorcontrib><creatorcontrib>Zhong, Pengzhen</creatorcontrib><creatorcontrib>Xie, Zhongpao</creatorcontrib><creatorcontrib>Zhou, Wei</creatorcontrib><creatorcontrib>Zhang, Chen</creatorcontrib><creatorcontrib>Cui, Dong-Mei</creatorcontrib><title>Ruthenium-catalyzed -alkylation of amino-1,3,5-triazines using alcohols</title><title>New journal of chemistry</title><description>An efficient ruthenium-catalyzed N -alkylation of amino 1,3,5-triazines with alcohols was achieved via a BH/HA strategy. Following this simple, facile, and high atom economical protocol, a broad range of products was prepared in moderate to good yields and heterocyclic or benzylic alcohols containing various functionalities were tolerated. The application of the reaction is also further demonstrated by the synthesis of alkylated secondary amine-1,3,5-triazines from olefinated amino-1,3,5-triazines and alcohols via a one pot N -alkylation and reductive reactions. An efficient ruthenium-catalyzed N -alkylation of amino-1,3,5-triazines with alcohols was achieved via BH/HA strategy.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFjrsKwjAUQIMoWB-Lu5APMJpr2khn8TGLe7n0YVPTRJJ0aL9eB8HR6Rw4yyFkBXwLXKS7AkzDBYDMRyQCIVOW7iWMPw5xzHgSyymZed9wDnCQEJHLrQt1aVTXshwD6n4oC8pQP3uNQVlDbUWxVcYy2IhNwoJTOChTetp5ZR4UdW5rq_2CTCrUvlx-OSfr8-l-vDLn8-zlVIuuz3534l9_A3RfPS4</recordid><startdate>20210913</startdate><enddate>20210913</enddate><creator>Zhao, Junna</creator><creator>Zhong, Pengzhen</creator><creator>Xie, Zhongpao</creator><creator>Zhou, Wei</creator><creator>Zhang, Chen</creator><creator>Cui, Dong-Mei</creator><scope/></search><sort><creationdate>20210913</creationdate><title>Ruthenium-catalyzed -alkylation of amino-1,3,5-triazines using alcohols</title><author>Zhao, Junna ; Zhong, Pengzhen ; Xie, Zhongpao ; Zhou, Wei ; Zhang, Chen ; Cui, Dong-Mei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_d1nj03116c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Junna</creatorcontrib><creatorcontrib>Zhong, Pengzhen</creatorcontrib><creatorcontrib>Xie, Zhongpao</creatorcontrib><creatorcontrib>Zhou, Wei</creatorcontrib><creatorcontrib>Zhang, Chen</creatorcontrib><creatorcontrib>Cui, Dong-Mei</creatorcontrib><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Junna</au><au>Zhong, Pengzhen</au><au>Xie, Zhongpao</au><au>Zhou, Wei</au><au>Zhang, Chen</au><au>Cui, Dong-Mei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ruthenium-catalyzed -alkylation of amino-1,3,5-triazines using alcohols</atitle><jtitle>New journal of chemistry</jtitle><date>2021-09-13</date><risdate>2021</risdate><volume>45</volume><issue>35</issue><spage>15776</spage><epage>15779</epage><pages>15776-15779</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>An efficient ruthenium-catalyzed N -alkylation of amino 1,3,5-triazines with alcohols was achieved via a BH/HA strategy. Following this simple, facile, and high atom economical protocol, a broad range of products was prepared in moderate to good yields and heterocyclic or benzylic alcohols containing various functionalities were tolerated. The application of the reaction is also further demonstrated by the synthesis of alkylated secondary amine-1,3,5-triazines from olefinated amino-1,3,5-triazines and alcohols via a one pot N -alkylation and reductive reactions. An efficient ruthenium-catalyzed N -alkylation of amino-1,3,5-triazines with alcohols was achieved via BH/HA strategy.</abstract><doi>10.1039/d1nj03116c</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1144-0546
ispartof New journal of chemistry, 2021-09, Vol.45 (35), p.15776-15779
issn 1144-0546
1369-9261
language
recordid cdi_rsc_primary_d1nj03116c
source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
title Ruthenium-catalyzed -alkylation of amino-1,3,5-triazines using alcohols
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T08%3A28%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ruthenium-catalyzed%20-alkylation%20of%20amino-1,3,5-triazines%20using%20alcohols&rft.jtitle=New%20journal%20of%20chemistry&rft.au=Zhao,%20Junna&rft.date=2021-09-13&rft.volume=45&rft.issue=35&rft.spage=15776&rft.epage=15779&rft.pages=15776-15779&rft.issn=1144-0546&rft.eissn=1369-9261&rft_id=info:doi/10.1039/d1nj03116c&rft_dat=%3Crsc%3Ed1nj03116c%3C/rsc%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