ChemInform Abstract: Studies in Selective 6-Membered Bromoether Formation via Bromonium and Thiiranium-Induced Cyclizations
Several methods for the synthesis of brominated 2,2,6,6‐tertasubstituted tetrahydropyrans are explored.
Gespeichert in:
Veröffentlicht in: | ChemInform 2015-09, Vol.46 (38), p.no-no |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | no |
---|---|
container_issue | 38 |
container_start_page | no |
container_title | ChemInform |
container_volume | 46 |
creator | Levinson, Adam M. Milner, Phillip J. Snyder, Scott A. |
description | Several methods for the synthesis of brominated 2,2,6,6‐tertasubstituted tetrahydropyrans are explored. |
doi_str_mv | 10.1002/chin.201538157 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1709467749</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3797574711</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1557-cf62335210eabc86d7577346b354f7478c4201cfaa88abd30bbff851563bb5e3</originalsourceid><addsrcrecordid>eNqFkEFP3DAQRi3USmxpr5wt9ZzFjmNPwg0CC1tROLBqpV4s25loTTcJ2Antwp9vliDUG6fRaN6b0XyEHHI254ylR27t23nKuBQ5l7BHZlymaZIqBR_IjBWCJyAL2CefYrwbeQF5OiPP5RqbZVt3oaEnNvbBuP6Y3vZD5TFS39Jb3KDr_SNSlXzHxmLAip6GrumwX2Ogi9E0ve9a-ujNNGj90FDTVnS19j6YXZss22pwo1lu3cY_vQjxM_lYm03EL6_1gKwW56vyMrm6uViWJ1eJ41JC4mqVCiFTztBYl6sKJIDIlBUyqyGD3GXj1642Js-NrQSztq5zyaUS1koUB-TrtPY-dA8Dxl7fdUNox4uaAysyBZAVIzWfKBe6GAPW-j74xoSt5kzv8tW7fPVbvqNQTMIfv8HtO7QuL5fX_7vJ5PrY498314TfWoEAqX9eX-hfix8Mvp2eaSb-AXnbj7Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1709467749</pqid></control><display><type>article</type><title>ChemInform Abstract: Studies in Selective 6-Membered Bromoether Formation via Bromonium and Thiiranium-Induced Cyclizations</title><source>Wiley Online Library All Journals</source><creator>Levinson, Adam M. ; Milner, Phillip J. ; Snyder, Scott A.</creator><creatorcontrib>Levinson, Adam M. ; Milner, Phillip J. ; Snyder, Scott A.</creatorcontrib><description>Several methods for the synthesis of brominated 2,2,6,6‐tertasubstituted tetrahydropyrans are explored.</description><identifier>ISSN: 0931-7597</identifier><identifier>EISSN: 1522-2667</identifier><identifier>DOI: 10.1002/chin.201538157</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>annulation reactions ; halogenation ; pyran derivatives ; ring closure reactions ; ring closure reactions, annulation reactions</subject><ispartof>ChemInform, 2015-09, Vol.46 (38), p.no-no</ispartof><rights>2015 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</rights><rights>2015 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1557-cf62335210eabc86d7577346b354f7478c4201cfaa88abd30bbff851563bb5e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchin.201538157$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchin.201538157$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids></links><search><creatorcontrib>Levinson, Adam M.</creatorcontrib><creatorcontrib>Milner, Phillip J.</creatorcontrib><creatorcontrib>Snyder, Scott A.</creatorcontrib><title>ChemInform Abstract: Studies in Selective 6-Membered Bromoether Formation via Bromonium and Thiiranium-Induced Cyclizations</title><title>ChemInform</title><addtitle>ChemInform</addtitle><description>Several methods for the synthesis of brominated 2,2,6,6‐tertasubstituted tetrahydropyrans are explored.</description><subject>annulation reactions</subject><subject>halogenation</subject><subject>pyran derivatives</subject><subject>ring closure reactions</subject><subject>ring closure reactions, annulation reactions</subject><issn>0931-7597</issn><issn>1522-2667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkEFP3DAQRi3USmxpr5wt9ZzFjmNPwg0CC1tROLBqpV4s25loTTcJ2Antwp9vliDUG6fRaN6b0XyEHHI254ylR27t23nKuBQ5l7BHZlymaZIqBR_IjBWCJyAL2CefYrwbeQF5OiPP5RqbZVt3oaEnNvbBuP6Y3vZD5TFS39Jb3KDr_SNSlXzHxmLAip6GrumwX2Ogi9E0ve9a-ujNNGj90FDTVnS19j6YXZss22pwo1lu3cY_vQjxM_lYm03EL6_1gKwW56vyMrm6uViWJ1eJ41JC4mqVCiFTztBYl6sKJIDIlBUyqyGD3GXj1642Js-NrQSztq5zyaUS1koUB-TrtPY-dA8Dxl7fdUNox4uaAysyBZAVIzWfKBe6GAPW-j74xoSt5kzv8tW7fPVbvqNQTMIfv8HtO7QuL5fX_7vJ5PrY498314TfWoEAqX9eX-hfix8Mvp2eaSb-AXnbj7Q</recordid><startdate>201509</startdate><enddate>201509</enddate><creator>Levinson, Adam M.</creator><creator>Milner, Phillip J.</creator><creator>Snyder, Scott A.</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201509</creationdate><title>ChemInform Abstract: Studies in Selective 6-Membered Bromoether Formation via Bromonium and Thiiranium-Induced Cyclizations</title><author>Levinson, Adam M. ; Milner, Phillip J. ; Snyder, Scott A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1557-cf62335210eabc86d7577346b354f7478c4201cfaa88abd30bbff851563bb5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>annulation reactions</topic><topic>halogenation</topic><topic>pyran derivatives</topic><topic>ring closure reactions</topic><topic>ring closure reactions, annulation reactions</topic><toplevel>online_resources</toplevel><creatorcontrib>Levinson, Adam M.</creatorcontrib><creatorcontrib>Milner, Phillip J.</creatorcontrib><creatorcontrib>Snyder, Scott A.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>ChemInform</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Levinson, Adam M.</au><au>Milner, Phillip J.</au><au>Snyder, Scott A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ChemInform Abstract: Studies in Selective 6-Membered Bromoether Formation via Bromonium and Thiiranium-Induced Cyclizations</atitle><jtitle>ChemInform</jtitle><addtitle>ChemInform</addtitle><date>2015-09</date><risdate>2015</risdate><volume>46</volume><issue>38</issue><spage>no</spage><epage>no</epage><pages>no-no</pages><issn>0931-7597</issn><eissn>1522-2667</eissn><abstract>Several methods for the synthesis of brominated 2,2,6,6‐tertasubstituted tetrahydropyrans are explored.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/chin.201538157</doi><tpages>1</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0931-7597 |
ispartof | ChemInform, 2015-09, Vol.46 (38), p.no-no |
issn | 0931-7597 1522-2667 |
language | eng |
recordid | cdi_proquest_journals_1709467749 |
source | Wiley Online Library All Journals |
subjects | annulation reactions halogenation pyran derivatives ring closure reactions ring closure reactions, annulation reactions |
title | ChemInform Abstract: Studies in Selective 6-Membered Bromoether Formation via Bromonium and Thiiranium-Induced Cyclizations |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T00%3A16%3A13IST&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=ChemInform%20Abstract:%20Studies%20in%20Selective%206-Membered%20Bromoether%20Formation%20via%20Bromonium%20and%20Thiiranium-Induced%20Cyclizations&rft.jtitle=ChemInform&rft.au=Levinson,%20Adam%20M.&rft.date=2015-09&rft.volume=46&rft.issue=38&rft.spage=no&rft.epage=no&rft.pages=no-no&rft.issn=0931-7597&rft.eissn=1522-2667&rft_id=info:doi/10.1002/chin.201538157&rft_dat=%3Cproquest_cross%3E3797574711%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=1709467749&rft_id=info:pmid/&rfr_iscdi=true |