ChemInform Abstract: An Environmentally Benign Synthesis of Octahydro-2H-chromen-4-ols via Modified Montmorillonite K10 Catalyzed Prins Cyclization Reaction

Montmorillonite K10 treated with HCl is employed as reusable solid acid for the reaction of (‐)‐isopulegol (I) with aldehydes and cyclohexanone.

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ChemInform 2013-09, Vol.44 (39), p.no-no
Hauptverfasser: Baishya, Gakul, Sarmah, Barnali, Hazarika, Nabajyoti
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 39
container_start_page no
container_title ChemInform
container_volume 44
creator Baishya, Gakul
Sarmah, Barnali
Hazarika, Nabajyoti
description Montmorillonite K10 treated with HCl is employed as reusable solid acid for the reaction of (‐)‐isopulegol (I) with aldehydes and cyclohexanone.
doi_str_mv 10.1002/chin.201339145
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1430179872</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3063071141</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1555-712a1bbfbc66451ff0b86071f9616b4840721d5083c5b36e3f07bba98160a1563</originalsourceid><addsrcrecordid>eNqFkU1v1DAQhiMEEkvhytkSZy8eO7YTbktauqt-8SmOlpO1iUvWLrZbmv6W_lhcLaq4cZqR5nlmRnqr6jWQJRBC3w6j80tKgLEWav6kWgCnFFMh5NNqQVoGWPJWPq9epHRZeCYbuqjuu9HsNt6GuEOrPuWoh_wOrTw68jcuBr8zPutpmtF7490Pj77MPo8muYSCRRdD1uO8jQHTNR7GGAqNaxymhG6cRmdh66wz29L4vAvRTVPwLht0AgR1uuyd78r0Y3Q-oW4eJnenswsefTbli9K8rJ5ZPSXz6m89qL59OPrarfHpxfGmW53iATjnWALV0Pe2H4SoOVhL-kYQCbYVIPq6qYmksOWkYQPvmTDMEtn3um1AEA1csIPqzX7vVQy_rk3K6jJcR19OKqgZAdk2khZquaeGGFKKxqqr6HY6zgqIekhAPSSgHhMoQrsXfrvJzP-hVbfenP_r4r3rUja3j66OP5WQTHL1_fxYSVKfnNWfDtUh-wMZm5qJ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1430179872</pqid></control><display><type>article</type><title>ChemInform Abstract: An Environmentally Benign Synthesis of Octahydro-2H-chromen-4-ols via Modified Montmorillonite K10 Catalyzed Prins Cyclization Reaction</title><source>Access via Wiley Online Library</source><creator>Baishya, Gakul ; Sarmah, Barnali ; Hazarika, Nabajyoti</creator><creatorcontrib>Baishya, Gakul ; Sarmah, Barnali ; Hazarika, Nabajyoti</creatorcontrib><description>Montmorillonite K10 treated with HCl is employed as reusable solid acid for the reaction of (‐)‐isopulegol (I) with aldehydes and cyclohexanone.</description><identifier>ISSN: 0931-7597</identifier><identifier>EISSN: 1522-2667</identifier><identifier>DOI: 10.1002/chin.201339145</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>benzopyran derivatives ; diastereoselective syntheses ; diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) ; enantioselective syntheses (incl. cis/trans-isomerism) ; mechanochemistry ; microwave chemistry ; microwave chemistry, sonochemistry, mechanochemistry ; ring closure reactions ; sonochemistry</subject><ispartof>ChemInform, 2013-09, Vol.44 (39), p.no-no</ispartof><rights>2013 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</rights><rights>2013 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1555-712a1bbfbc66451ff0b86071f9616b4840721d5083c5b36e3f07bba98160a1563</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.201339145$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchin.201339145$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids></links><search><creatorcontrib>Baishya, Gakul</creatorcontrib><creatorcontrib>Sarmah, Barnali</creatorcontrib><creatorcontrib>Hazarika, Nabajyoti</creatorcontrib><title>ChemInform Abstract: An Environmentally Benign Synthesis of Octahydro-2H-chromen-4-ols via Modified Montmorillonite K10 Catalyzed Prins Cyclization Reaction</title><title>ChemInform</title><addtitle>ChemInform</addtitle><description>Montmorillonite K10 treated with HCl is employed as reusable solid acid for the reaction of (‐)‐isopulegol (I) with aldehydes and cyclohexanone.</description><subject>benzopyran derivatives</subject><subject>diastereoselective syntheses</subject><subject>diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)</subject><subject>enantioselective syntheses (incl. cis/trans-isomerism)</subject><subject>mechanochemistry</subject><subject>microwave chemistry</subject><subject>microwave chemistry, sonochemistry, mechanochemistry</subject><subject>ring closure reactions</subject><subject>sonochemistry</subject><issn>0931-7597</issn><issn>1522-2667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQhiMEEkvhytkSZy8eO7YTbktauqt-8SmOlpO1iUvWLrZbmv6W_lhcLaq4cZqR5nlmRnqr6jWQJRBC3w6j80tKgLEWav6kWgCnFFMh5NNqQVoGWPJWPq9epHRZeCYbuqjuu9HsNt6GuEOrPuWoh_wOrTw68jcuBr8zPutpmtF7490Pj77MPo8muYSCRRdD1uO8jQHTNR7GGAqNaxymhG6cRmdh66wz29L4vAvRTVPwLht0AgR1uuyd78r0Y3Q-oW4eJnenswsefTbli9K8rJ5ZPSXz6m89qL59OPrarfHpxfGmW53iATjnWALV0Pe2H4SoOVhL-kYQCbYVIPq6qYmksOWkYQPvmTDMEtn3um1AEA1csIPqzX7vVQy_rk3K6jJcR19OKqgZAdk2khZquaeGGFKKxqqr6HY6zgqIekhAPSSgHhMoQrsXfrvJzP-hVbfenP_r4r3rUja3j66OP5WQTHL1_fxYSVKfnNWfDtUh-wMZm5qJ</recordid><startdate>20130924</startdate><enddate>20130924</enddate><creator>Baishya, Gakul</creator><creator>Sarmah, Barnali</creator><creator>Hazarika, Nabajyoti</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>20130924</creationdate><title>ChemInform Abstract: An Environmentally Benign Synthesis of Octahydro-2H-chromen-4-ols via Modified Montmorillonite K10 Catalyzed Prins Cyclization Reaction</title><author>Baishya, Gakul ; Sarmah, Barnali ; Hazarika, Nabajyoti</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1555-712a1bbfbc66451ff0b86071f9616b4840721d5083c5b36e3f07bba98160a1563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>benzopyran derivatives</topic><topic>diastereoselective syntheses</topic><topic>diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)</topic><topic>enantioselective syntheses (incl. cis/trans-isomerism)</topic><topic>mechanochemistry</topic><topic>microwave chemistry</topic><topic>microwave chemistry, sonochemistry, mechanochemistry</topic><topic>ring closure reactions</topic><topic>sonochemistry</topic><toplevel>online_resources</toplevel><creatorcontrib>Baishya, Gakul</creatorcontrib><creatorcontrib>Sarmah, Barnali</creatorcontrib><creatorcontrib>Hazarika, Nabajyoti</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>ChemInform</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baishya, Gakul</au><au>Sarmah, Barnali</au><au>Hazarika, Nabajyoti</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ChemInform Abstract: An Environmentally Benign Synthesis of Octahydro-2H-chromen-4-ols via Modified Montmorillonite K10 Catalyzed Prins Cyclization Reaction</atitle><jtitle>ChemInform</jtitle><addtitle>ChemInform</addtitle><date>2013-09-24</date><risdate>2013</risdate><volume>44</volume><issue>39</issue><spage>no</spage><epage>no</epage><pages>no-no</pages><issn>0931-7597</issn><eissn>1522-2667</eissn><abstract>Montmorillonite K10 treated with HCl is employed as reusable solid acid for the reaction of (‐)‐isopulegol (I) with aldehydes and cyclohexanone.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/chin.201339145</doi><tpages>1</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0931-7597
ispartof ChemInform, 2013-09, Vol.44 (39), p.no-no
issn 0931-7597
1522-2667
language eng
recordid cdi_proquest_journals_1430179872
source Access via Wiley Online Library
subjects benzopyran derivatives
diastereoselective syntheses
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
enantioselective syntheses (incl. cis/trans-isomerism)
mechanochemistry
microwave chemistry
microwave chemistry, sonochemistry, mechanochemistry
ring closure reactions
sonochemistry
title ChemInform Abstract: An Environmentally Benign Synthesis of Octahydro-2H-chromen-4-ols via Modified Montmorillonite K10 Catalyzed Prins Cyclization Reaction
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-12T13%3A52%3A57IST&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:%20An%20Environmentally%20Benign%20Synthesis%20of%20Octahydro-2H-chromen-4-ols%20via%20Modified%20Montmorillonite%20K10%20Catalyzed%20Prins%20Cyclization%20Reaction&rft.jtitle=ChemInform&rft.au=Baishya,%20Gakul&rft.date=2013-09-24&rft.volume=44&rft.issue=39&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.201339145&rft_dat=%3Cproquest_cross%3E3063071141%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=1430179872&rft_id=info:pmid/&rfr_iscdi=true