Synthesis of 1,4-diazepinone derivatives a domino aza-Michael/S2 cyclization of 1-azadienes with α-halogenoacetamides
A novel cyclization of α-halogenoacetamides with 1-azadienes has been developed for the efficient preparation of monocyclic 1,4-diazepinones in one step under transition metal-free conditions. Various α-halogenoacetamides and 1-azadienes are well tolerated and give the desired products in good to ex...
Gespeichert in:
Veröffentlicht in: | Organic & biomolecular chemistry 2020-02, Vol.18 (6), p.182-186 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 186 |
---|---|
container_issue | 6 |
container_start_page | 182 |
container_title | Organic & biomolecular chemistry |
container_volume | 18 |
creator | Yuan, Chunhao Zhang, Hui Yuan, Mengna Xie, Lei Cao, Xiaoqun |
description | A novel cyclization of α-halogenoacetamides with 1-azadienes has been developed for the efficient preparation of monocyclic 1,4-diazepinones in one step under transition metal-free conditions. Various α-halogenoacetamides and 1-azadienes are well tolerated and give the desired products in good to excellent yields. This cyclization also demonstrates potential synthetic utility on a gram-scale and further transformation.
A novel cyclization of
N
-alkoxy α-halogenoacetamides with
N
-sulfonyl-1-aza-1,3-butadienes has been developed for the efficient preparation of 1,4-diazepinones in one step under transition metal-free conditions. |
doi_str_mv | 10.1039/c9ob02626f |
format | Article |
fullrecord | <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c9ob02626f</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c9ob02626f</sourcerecordid><originalsourceid>FETCH-rsc_primary_c9ob02626f3</originalsourceid><addsrcrecordid>eNp9T7tuwjAUtaoilUIXdiR3x2AnIVHmqhULE-zRxb5pLkrsKI5SJX_Fj_BNTauqbEzn6Lykw9hCybWSYbrRqTvJIA7i_IFNVZQkQm7D9PGfB_KJPXt_llKlSRxNWXfobVugJ89dztUqEoZgwJqss8gNNtRBSx16Dty4apQ5DCD2pAvAcnMIuO51ScMYcvZ3Qoy-IbRj5Yvagl8vooDSfaJ1oLGFigz6OZvkUHp8-cMZW368H992ovE6qxuqoOmz25lwxl7v-VltfjL3N74BjJ5atQ</addsrcrecordid><sourcetype>Enrichment Source</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis of 1,4-diazepinone derivatives a domino aza-Michael/S2 cyclization of 1-azadienes with α-halogenoacetamides</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Yuan, Chunhao ; Zhang, Hui ; Yuan, Mengna ; Xie, Lei ; Cao, Xiaoqun</creator><creatorcontrib>Yuan, Chunhao ; Zhang, Hui ; Yuan, Mengna ; Xie, Lei ; Cao, Xiaoqun</creatorcontrib><description>A novel cyclization of α-halogenoacetamides with 1-azadienes has been developed for the efficient preparation of monocyclic 1,4-diazepinones in one step under transition metal-free conditions. Various α-halogenoacetamides and 1-azadienes are well tolerated and give the desired products in good to excellent yields. This cyclization also demonstrates potential synthetic utility on a gram-scale and further transformation.
A novel cyclization of
N
-alkoxy α-halogenoacetamides with
N
-sulfonyl-1-aza-1,3-butadienes has been developed for the efficient preparation of 1,4-diazepinones in one step under transition metal-free conditions.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/c9ob02626f</identifier><language>eng</language><ispartof>Organic & biomolecular chemistry, 2020-02, Vol.18 (6), p.182-186</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>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Yuan, Chunhao</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><creatorcontrib>Yuan, Mengna</creatorcontrib><creatorcontrib>Xie, Lei</creatorcontrib><creatorcontrib>Cao, Xiaoqun</creatorcontrib><title>Synthesis of 1,4-diazepinone derivatives a domino aza-Michael/S2 cyclization of 1-azadienes with α-halogenoacetamides</title><title>Organic & biomolecular chemistry</title><description>A novel cyclization of α-halogenoacetamides with 1-azadienes has been developed for the efficient preparation of monocyclic 1,4-diazepinones in one step under transition metal-free conditions. Various α-halogenoacetamides and 1-azadienes are well tolerated and give the desired products in good to excellent yields. This cyclization also demonstrates potential synthetic utility on a gram-scale and further transformation.
A novel cyclization of
N
-alkoxy α-halogenoacetamides with
N
-sulfonyl-1-aza-1,3-butadienes has been developed for the efficient preparation of 1,4-diazepinones in one step under transition metal-free conditions.</description><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNp9T7tuwjAUtaoilUIXdiR3x2AnIVHmqhULE-zRxb5pLkrsKI5SJX_Fj_BNTauqbEzn6Lykw9hCybWSYbrRqTvJIA7i_IFNVZQkQm7D9PGfB_KJPXt_llKlSRxNWXfobVugJ89dztUqEoZgwJqss8gNNtRBSx16Dty4apQ5DCD2pAvAcnMIuO51ScMYcvZ3Qoy-IbRj5Yvagl8vooDSfaJ1oLGFigz6OZvkUHp8-cMZW368H992ovE6qxuqoOmz25lwxl7v-VltfjL3N74BjJ5atQ</recordid><startdate>20200212</startdate><enddate>20200212</enddate><creator>Yuan, Chunhao</creator><creator>Zhang, Hui</creator><creator>Yuan, Mengna</creator><creator>Xie, Lei</creator><creator>Cao, Xiaoqun</creator><scope/></search><sort><creationdate>20200212</creationdate><title>Synthesis of 1,4-diazepinone derivatives a domino aza-Michael/S2 cyclization of 1-azadienes with α-halogenoacetamides</title><author>Yuan, Chunhao ; Zhang, Hui ; Yuan, Mengna ; Xie, Lei ; Cao, Xiaoqun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c9ob02626f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yuan, Chunhao</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><creatorcontrib>Yuan, Mengna</creatorcontrib><creatorcontrib>Xie, Lei</creatorcontrib><creatorcontrib>Cao, Xiaoqun</creatorcontrib><jtitle>Organic & biomolecular chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yuan, Chunhao</au><au>Zhang, Hui</au><au>Yuan, Mengna</au><au>Xie, Lei</au><au>Cao, Xiaoqun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of 1,4-diazepinone derivatives a domino aza-Michael/S2 cyclization of 1-azadienes with α-halogenoacetamides</atitle><jtitle>Organic & biomolecular chemistry</jtitle><date>2020-02-12</date><risdate>2020</risdate><volume>18</volume><issue>6</issue><spage>182</spage><epage>186</epage><pages>182-186</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>A novel cyclization of α-halogenoacetamides with 1-azadienes has been developed for the efficient preparation of monocyclic 1,4-diazepinones in one step under transition metal-free conditions. Various α-halogenoacetamides and 1-azadienes are well tolerated and give the desired products in good to excellent yields. This cyclization also demonstrates potential synthetic utility on a gram-scale and further transformation.
A novel cyclization of
N
-alkoxy α-halogenoacetamides with
N
-sulfonyl-1-aza-1,3-butadienes has been developed for the efficient preparation of 1,4-diazepinones in one step under transition metal-free conditions.</abstract><doi>10.1039/c9ob02626f</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1477-0520 |
ispartof | Organic & biomolecular chemistry, 2020-02, Vol.18 (6), p.182-186 |
issn | 1477-0520 1477-0539 |
language | eng |
recordid | cdi_rsc_primary_c9ob02626f |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Synthesis of 1,4-diazepinone derivatives a domino aza-Michael/S2 cyclization of 1-azadienes with α-halogenoacetamides |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T04%3A15%3A39IST&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=Synthesis%20of%201,4-diazepinone%20derivatives%20a%20domino%20aza-Michael/S2%20cyclization%20of%201-azadienes%20with%20%CE%B1-halogenoacetamides&rft.jtitle=Organic%20&%20biomolecular%20chemistry&rft.au=Yuan,%20Chunhao&rft.date=2020-02-12&rft.volume=18&rft.issue=6&rft.spage=182&rft.epage=186&rft.pages=182-186&rft.issn=1477-0520&rft.eissn=1477-0539&rft_id=info:doi/10.1039/c9ob02626f&rft_dat=%3Crsc%3Ec9ob02626f%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 |