The First Synthesis of a Novel 5:7:5-Fused Diimidazodiazepine Ring System and Some of Its Chemical Properties
The first synthesis of a novel 5:7:5-fused heterocyclic ring system, a diimidazodiazepine, is reported. The propensity of the ring system to undergo facile, acid-catalyzed nucleophilic addition reactions by neutral carbon and nitrogen nucleophiles has been explored. The ring system has potential fut...
Gespeichert in:
Veröffentlicht in: | Organic letters 2008-10, Vol.10 (20), p.4681-4684 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 4684 |
---|---|
container_issue | 20 |
container_start_page | 4681 |
container_title | Organic letters |
container_volume | 10 |
creator | Kumar, Raj Ujjinamatada, Ravi K Hosmane, Ramachandra S |
description | The first synthesis of a novel 5:7:5-fused heterocyclic ring system, a diimidazodiazepine, is reported. The propensity of the ring system to undergo facile, acid-catalyzed nucleophilic addition reactions by neutral carbon and nitrogen nucleophiles has been explored. The ring system has potential future applications in mechanistic studies of formation and repair of DNA interstrand cross-links. |
doi_str_mv | 10.1021/ol8020176 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2652043</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>69643317</sourcerecordid><originalsourceid>FETCH-LOGICAL-a403t-f51393a051c3aaeef80582944b016930e5a115f1702a1a2b2bf6b0c7f871d9b43</originalsourceid><addsrcrecordid>eNptkU1v1DAQhi1URD_gwB9AvhSph8CME-ejByS0dEulChAtZ2uSTLquknhrJ5XaX19Xu9qCxGlGM8-89swrxHuETwgKP7u-BAVY5K_EAWqVJgVotbfLc9gXhyHcAmCsVG_EPpYl5qjKAzFcr1gurQ-TvHoYpxUHG6TrJMkf7p57qU-LU50s58Ct_GbtYFt6dK2lR17bkeVvO97EwTDxIGls5ZUb-Hn8YgpyseLBNtTLX96t2U-Ww1vxuqM-8LttPBJ_lmfXi-_J5c_zi8XXy4QySKek05hWKYHGJiVi7krQpaqyrAbMqxRYU9ykwwIUIala1V1eQ1N0ZYFtVWfpkfiy0V3P9cBtw-PkqTdrbwfyD8aRNf92RrsyN-7eqFwryNIo8HEr4N3dzGEygw0N9z2N7OZg8iqPFBYRPNmAjXcheO52jyCYZ3PMzpzIfvj7Vy_k1o0IHG8AaoK5dbMf45H-I_QETieVjw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>69643317</pqid></control><display><type>article</type><title>The First Synthesis of a Novel 5:7:5-Fused Diimidazodiazepine Ring System and Some of Its Chemical Properties</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Kumar, Raj ; Ujjinamatada, Ravi K ; Hosmane, Ramachandra S</creator><creatorcontrib>Kumar, Raj ; Ujjinamatada, Ravi K ; Hosmane, Ramachandra S</creatorcontrib><description>The first synthesis of a novel 5:7:5-fused heterocyclic ring system, a diimidazodiazepine, is reported. The propensity of the ring system to undergo facile, acid-catalyzed nucleophilic addition reactions by neutral carbon and nitrogen nucleophiles has been explored. The ring system has potential future applications in mechanistic studies of formation and repair of DNA interstrand cross-links.</description><identifier>ISSN: 1523-7060</identifier><identifier>EISSN: 1523-7052</identifier><identifier>DOI: 10.1021/ol8020176</identifier><identifier>PMID: 18816128</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Azepines - chemical synthesis ; Azepines - chemistry ; Imidazoles - chemistry ; Magnetic Resonance Spectroscopy ; Molecular Structure</subject><ispartof>Organic letters, 2008-10, Vol.10 (20), p.4681-4684</ispartof><rights>Copyright © 2008 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a403t-f51393a051c3aaeef80582944b016930e5a115f1702a1a2b2bf6b0c7f871d9b43</citedby><cites>FETCH-LOGICAL-a403t-f51393a051c3aaeef80582944b016930e5a115f1702a1a2b2bf6b0c7f871d9b43</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/ol8020176$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ol8020176$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,780,784,885,2756,27067,27915,27916,56729,56779</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18816128$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kumar, Raj</creatorcontrib><creatorcontrib>Ujjinamatada, Ravi K</creatorcontrib><creatorcontrib>Hosmane, Ramachandra S</creatorcontrib><title>The First Synthesis of a Novel 5:7:5-Fused Diimidazodiazepine Ring System and Some of Its Chemical Properties</title><title>Organic letters</title><addtitle>Org. Lett</addtitle><description>The first synthesis of a novel 5:7:5-fused heterocyclic ring system, a diimidazodiazepine, is reported. The propensity of the ring system to undergo facile, acid-catalyzed nucleophilic addition reactions by neutral carbon and nitrogen nucleophiles has been explored. The ring system has potential future applications in mechanistic studies of formation and repair of DNA interstrand cross-links.</description><subject>Azepines - chemical synthesis</subject><subject>Azepines - chemistry</subject><subject>Imidazoles - chemistry</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Molecular Structure</subject><issn>1523-7060</issn><issn>1523-7052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkU1v1DAQhi1URD_gwB9AvhSph8CME-ejByS0dEulChAtZ2uSTLquknhrJ5XaX19Xu9qCxGlGM8-89swrxHuETwgKP7u-BAVY5K_EAWqVJgVotbfLc9gXhyHcAmCsVG_EPpYl5qjKAzFcr1gurQ-TvHoYpxUHG6TrJMkf7p57qU-LU50s58Ct_GbtYFt6dK2lR17bkeVvO97EwTDxIGls5ZUb-Hn8YgpyseLBNtTLX96t2U-Ww1vxuqM-8LttPBJ_lmfXi-_J5c_zi8XXy4QySKek05hWKYHGJiVi7krQpaqyrAbMqxRYU9ykwwIUIala1V1eQ1N0ZYFtVWfpkfiy0V3P9cBtw-PkqTdrbwfyD8aRNf92RrsyN-7eqFwryNIo8HEr4N3dzGEygw0N9z2N7OZg8iqPFBYRPNmAjXcheO52jyCYZ3PMzpzIfvj7Vy_k1o0IHG8AaoK5dbMf45H-I_QETieVjw</recordid><startdate>20081016</startdate><enddate>20081016</enddate><creator>Kumar, Raj</creator><creator>Ujjinamatada, Ravi K</creator><creator>Hosmane, Ramachandra S</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20081016</creationdate><title>The First Synthesis of a Novel 5:7:5-Fused Diimidazodiazepine Ring System and Some of Its Chemical Properties</title><author>Kumar, Raj ; Ujjinamatada, Ravi K ; Hosmane, Ramachandra S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a403t-f51393a051c3aaeef80582944b016930e5a115f1702a1a2b2bf6b0c7f871d9b43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Azepines - chemical synthesis</topic><topic>Azepines - chemistry</topic><topic>Imidazoles - chemistry</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Molecular Structure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumar, Raj</creatorcontrib><creatorcontrib>Ujjinamatada, Ravi K</creatorcontrib><creatorcontrib>Hosmane, Ramachandra S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Organic letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumar, Raj</au><au>Ujjinamatada, Ravi K</au><au>Hosmane, Ramachandra S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The First Synthesis of a Novel 5:7:5-Fused Diimidazodiazepine Ring System and Some of Its Chemical Properties</atitle><jtitle>Organic letters</jtitle><addtitle>Org. Lett</addtitle><date>2008-10-16</date><risdate>2008</risdate><volume>10</volume><issue>20</issue><spage>4681</spage><epage>4684</epage><pages>4681-4684</pages><issn>1523-7060</issn><eissn>1523-7052</eissn><abstract>The first synthesis of a novel 5:7:5-fused heterocyclic ring system, a diimidazodiazepine, is reported. The propensity of the ring system to undergo facile, acid-catalyzed nucleophilic addition reactions by neutral carbon and nitrogen nucleophiles has been explored. The ring system has potential future applications in mechanistic studies of formation and repair of DNA interstrand cross-links.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>18816128</pmid><doi>10.1021/ol8020176</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1523-7060 |
ispartof | Organic letters, 2008-10, Vol.10 (20), p.4681-4684 |
issn | 1523-7060 1523-7052 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2652043 |
source | MEDLINE; American Chemical Society Journals |
subjects | Azepines - chemical synthesis Azepines - chemistry Imidazoles - chemistry Magnetic Resonance Spectroscopy Molecular Structure |
title | The First Synthesis of a Novel 5:7:5-Fused Diimidazodiazepine Ring System and Some of Its Chemical Properties |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T19%3A10%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20First%20Synthesis%20of%20a%20Novel%205:7:5-Fused%20Diimidazodiazepine%20Ring%20System%20and%20Some%20of%20Its%20Chemical%20Properties&rft.jtitle=Organic%20letters&rft.au=Kumar,%20Raj&rft.date=2008-10-16&rft.volume=10&rft.issue=20&rft.spage=4681&rft.epage=4684&rft.pages=4681-4684&rft.issn=1523-7060&rft.eissn=1523-7052&rft_id=info:doi/10.1021/ol8020176&rft_dat=%3Cproquest_pubme%3E69643317%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=69643317&rft_id=info:pmid/18816128&rfr_iscdi=true |