A facile and practical copper diacetate mediated, ligand free C-N cross coupling of trivalent organobismuth compounds with amines and N-heteroarenes
In present work, an efficient Cu(OAc) 2 ·H 2 O catalyzed protocol in the absence of any additional ligand has been developed for the N -arylation of amines and nitrogen containing heterocycles using trivalent organobismuth reagents under mild conditions. This protocol tolerates a variety of function...
Gespeichert in:
Veröffentlicht in: | RSC advances 2016-01, Vol.6 (18), p.14531-14537 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 14537 |
---|---|
container_issue | 18 |
container_start_page | 14531 |
container_title | RSC advances |
container_volume | 6 |
creator | Jadhav, B. D Pardeshi, S. K |
description | In present work, an efficient Cu(OAc)
2
·H
2
O catalyzed protocol in the absence of any additional ligand has been developed for the
N
-arylation of amines and nitrogen containing heterocycles using trivalent organobismuth reagents under mild conditions. This protocol tolerates a variety of functional groups on amines and the organobismuth reagent with a high degree of chemoselectivity.
In present work, an efficient Cu(OAc)
2
·H
2
O catalyzed protocol in the absence of any additional ligand has been developed for the
N
-arylation of amines and nitrogen containing heterocycles using trivalent organobismuth reagents under mild conditions. |
doi_str_mv | 10.1039/c6ra00395h |
format | Article |
fullrecord | <record><control><sourceid>proquest_rsc_p</sourceid><recordid>TN_cdi_rsc_primary_c6ra00395h</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1800479290</sourcerecordid><originalsourceid>FETCH-LOGICAL-c286t-fbe16c18b9931416356e2b80a1afd3b68bea9feaa63e8dbb09d25a841852857c3</originalsourceid><addsrcrecordid>eNpNkU1PwzAMhiMEEtPYhTtSjghRSPqRpcepAoaEhoTgXLmpuwW1TUlSEP-DH0y2IcAXv7Ye27JNyClnV5wl-bUSFlgQ2eaATGKWiihmIj_8p4_JzLlXFkxkPBZ8Qr4WtAGlW6TQ13SwoLxW0FJlhgEtrTUo9OCRdhi0x_qStnq9ZRuLSItoRZU1zoWCcWh1v6amod7qd2ix99TYwJpKu270m8B0gxn72tEPHULodI9uN3gVbdCjNWAxpE7IUQOtw9mPn5KX25vnYhk9PN7dF4uHSMVS-KipkAvFZZXnCU-5SDKBcSUZcGjqpBKyQsgbBBAJyrqqWF7HGciUyyyW2VwlU3K-7ztY8zai82WnncK2hR7N6EouGUvneZyzgF7s0d22FptysLoD-1lyVm6vXxbiabG7_jLAZ3vYOvXL_X0n-QZfqIPu</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1800479290</pqid></control><display><type>article</type><title>A facile and practical copper diacetate mediated, ligand free C-N cross coupling of trivalent organobismuth compounds with amines and N-heteroarenes</title><source>Royal Society Of Chemistry Journals</source><creator>Jadhav, B. D ; Pardeshi, S. K</creator><creatorcontrib>Jadhav, B. D ; Pardeshi, S. K</creatorcontrib><description>In present work, an efficient Cu(OAc)
2
·H
2
O catalyzed protocol in the absence of any additional ligand has been developed for the
N
-arylation of amines and nitrogen containing heterocycles using trivalent organobismuth reagents under mild conditions. This protocol tolerates a variety of functional groups on amines and the organobismuth reagent with a high degree of chemoselectivity.
In present work, an efficient Cu(OAc)
2
·H
2
O catalyzed protocol in the absence of any additional ligand has been developed for the
N
-arylation of amines and nitrogen containing heterocycles using trivalent organobismuth reagents under mild conditions.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/c6ra00395h</identifier><language>eng</language><subject>Amines ; Copper ; Copper compounds ; Cross coupling ; Functional groups ; Ligands ; Reagents</subject><ispartof>RSC advances, 2016-01, Vol.6 (18), p.14531-14537</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c286t-fbe16c18b9931416356e2b80a1afd3b68bea9feaa63e8dbb09d25a841852857c3</citedby><cites>FETCH-LOGICAL-c286t-fbe16c18b9931416356e2b80a1afd3b68bea9feaa63e8dbb09d25a841852857c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Jadhav, B. D</creatorcontrib><creatorcontrib>Pardeshi, S. K</creatorcontrib><title>A facile and practical copper diacetate mediated, ligand free C-N cross coupling of trivalent organobismuth compounds with amines and N-heteroarenes</title><title>RSC advances</title><description>In present work, an efficient Cu(OAc)
2
·H
2
O catalyzed protocol in the absence of any additional ligand has been developed for the
N
-arylation of amines and nitrogen containing heterocycles using trivalent organobismuth reagents under mild conditions. This protocol tolerates a variety of functional groups on amines and the organobismuth reagent with a high degree of chemoselectivity.
In present work, an efficient Cu(OAc)
2
·H
2
O catalyzed protocol in the absence of any additional ligand has been developed for the
N
-arylation of amines and nitrogen containing heterocycles using trivalent organobismuth reagents under mild conditions.</description><subject>Amines</subject><subject>Copper</subject><subject>Copper compounds</subject><subject>Cross coupling</subject><subject>Functional groups</subject><subject>Ligands</subject><subject>Reagents</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpNkU1PwzAMhiMEEtPYhTtSjghRSPqRpcepAoaEhoTgXLmpuwW1TUlSEP-DH0y2IcAXv7Ye27JNyClnV5wl-bUSFlgQ2eaATGKWiihmIj_8p4_JzLlXFkxkPBZ8Qr4WtAGlW6TQ13SwoLxW0FJlhgEtrTUo9OCRdhi0x_qStnq9ZRuLSItoRZU1zoWCcWh1v6amod7qd2ix99TYwJpKu270m8B0gxn72tEPHULodI9uN3gVbdCjNWAxpE7IUQOtw9mPn5KX25vnYhk9PN7dF4uHSMVS-KipkAvFZZXnCU-5SDKBcSUZcGjqpBKyQsgbBBAJyrqqWF7HGciUyyyW2VwlU3K-7ztY8zai82WnncK2hR7N6EouGUvneZyzgF7s0d22FptysLoD-1lyVm6vXxbiabG7_jLAZ3vYOvXL_X0n-QZfqIPu</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Jadhav, B. D</creator><creator>Pardeshi, S. K</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20160101</creationdate><title>A facile and practical copper diacetate mediated, ligand free C-N cross coupling of trivalent organobismuth compounds with amines and N-heteroarenes</title><author>Jadhav, B. D ; Pardeshi, S. K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c286t-fbe16c18b9931416356e2b80a1afd3b68bea9feaa63e8dbb09d25a841852857c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Amines</topic><topic>Copper</topic><topic>Copper compounds</topic><topic>Cross coupling</topic><topic>Functional groups</topic><topic>Ligands</topic><topic>Reagents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jadhav, B. D</creatorcontrib><creatorcontrib>Pardeshi, S. K</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jadhav, B. D</au><au>Pardeshi, S. K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A facile and practical copper diacetate mediated, ligand free C-N cross coupling of trivalent organobismuth compounds with amines and N-heteroarenes</atitle><jtitle>RSC advances</jtitle><date>2016-01-01</date><risdate>2016</risdate><volume>6</volume><issue>18</issue><spage>14531</spage><epage>14537</epage><pages>14531-14537</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>In present work, an efficient Cu(OAc)
2
·H
2
O catalyzed protocol in the absence of any additional ligand has been developed for the
N
-arylation of amines and nitrogen containing heterocycles using trivalent organobismuth reagents under mild conditions. This protocol tolerates a variety of functional groups on amines and the organobismuth reagent with a high degree of chemoselectivity.
In present work, an efficient Cu(OAc)
2
·H
2
O catalyzed protocol in the absence of any additional ligand has been developed for the
N
-arylation of amines and nitrogen containing heterocycles using trivalent organobismuth reagents under mild conditions.</abstract><doi>10.1039/c6ra00395h</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2046-2069 |
ispartof | RSC advances, 2016-01, Vol.6 (18), p.14531-14537 |
issn | 2046-2069 2046-2069 |
language | eng |
recordid | cdi_rsc_primary_c6ra00395h |
source | Royal Society Of Chemistry Journals |
subjects | Amines Copper Copper compounds Cross coupling Functional groups Ligands Reagents |
title | A facile and practical copper diacetate mediated, ligand free C-N cross coupling of trivalent organobismuth compounds with amines and N-heteroarenes |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T15%3A28%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_rsc_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20facile%20and%20practical%20copper%20diacetate%20mediated,%20ligand%20free%20C-N%20cross%20coupling%20of%20trivalent%20organobismuth%20compounds%20with%20amines%20and%20N-heteroarenes&rft.jtitle=RSC%20advances&rft.au=Jadhav,%20B.%20D&rft.date=2016-01-01&rft.volume=6&rft.issue=18&rft.spage=14531&rft.epage=14537&rft.pages=14531-14537&rft.issn=2046-2069&rft.eissn=2046-2069&rft_id=info:doi/10.1039/c6ra00395h&rft_dat=%3Cproquest_rsc_p%3E1800479290%3C/proquest_rsc_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1800479290&rft_id=info:pmid/&rfr_iscdi=true |