A mild and efficient synthesis of chiral tetrahydroquinolino pyranose derivatives catalyzed by lanthanum(iii) nitrate hexahydrate
A mild and highly efficient synthesis of chiral tetrahydroquinolino pyranose derivatives is described. The reaction of a chiral α,β‐unsaturated aldehyde containing a hydroxyl group with different aryl amines using lanthanum(III) nitrate hexahydrate as a catalyst afforded corresponding chiral tetrahy...
Gespeichert in:
| Veröffentlicht in: | Heteroatom chemistry 2008-05, Vol.19 (4), p.429-433 |
|---|---|
| Hauptverfasser: | , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 433 |
|---|---|
| container_issue | 4 |
| container_start_page | 429 |
| container_title | Heteroatom chemistry |
| container_volume | 19 |
| creator | Narasimhulu, M. Reddy, S. Malla Rajesh, K. Suryakiran, N. Ramesh, D. Venkateswarlu, Y. |
| description | A mild and highly efficient synthesis of chiral tetrahydroquinolino pyranose derivatives is described. The reaction of a chiral α,β‐unsaturated aldehyde containing a hydroxyl group with different aryl amines using lanthanum(III) nitrate hexahydrate as a catalyst afforded corresponding chiral tetrahydroquinolinated pyranosides in excellent yields. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:429–433, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20441 |
| doi_str_mv | 10.1002/hc.20441 |
| format | Article |
| fullrecord | <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_hc_20441</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_44P7JM5X_S</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3371-df4250f08c78cab082923f85a64c66825e1f4f7b642d3bccd2603862ef57262f3</originalsourceid><addsrcrecordid>eNp1kLtOwzAARSMEEqUg8Qkey5DiV2x3rCpoQeUhAYLNch1bMaRJsd3SsPHnpC1iQGK4unc4OsNNklME-whCfF7oPoaUor2kg-BApAhytL_ZFKccMXKYHIXwCiFCdCA6ydcQzF2ZA1XlwFjrtDNVBKGpYmGCC6C2QBfOqxJEE70qmtzX70tX1WUbsGi8qupgQG68W6noViYAraIqm0-Tg1kDStWaVLWc95xzZ6ByrSQaUJj11tXu4-TAqjKYk5_uJk-XF4-jSTq9G1-NhtNUE8JRmluKM2ih0FxoNYMCDzCxIlOMasYEzgyy1PIZozgnM61zzCARDBubccywJd2kt_NqX4fgjZUL7-bKNxJBublOFlpur2vRdId-uNI0_3JyMvrDuxDN-pdX_k0yTngmn2_HktJ7fn2TvcgH8g17LYEY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A mild and efficient synthesis of chiral tetrahydroquinolino pyranose derivatives catalyzed by lanthanum(iii) nitrate hexahydrate</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Narasimhulu, M. ; Reddy, S. Malla ; Rajesh, K. ; Suryakiran, N. ; Ramesh, D. ; Venkateswarlu, Y.</creator><creatorcontrib>Narasimhulu, M. ; Reddy, S. Malla ; Rajesh, K. ; Suryakiran, N. ; Ramesh, D. ; Venkateswarlu, Y.</creatorcontrib><description>A mild and highly efficient synthesis of chiral tetrahydroquinolino pyranose derivatives is described. The reaction of a chiral α,β‐unsaturated aldehyde containing a hydroxyl group with different aryl amines using lanthanum(III) nitrate hexahydrate as a catalyst afforded corresponding chiral tetrahydroquinolinated pyranosides in excellent yields. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:429–433, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20441</description><identifier>ISSN: 1042-7163</identifier><identifier>EISSN: 1098-1071</identifier><identifier>DOI: 10.1002/hc.20441</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><ispartof>Heteroatom chemistry, 2008-05, Vol.19 (4), p.429-433</ispartof><rights>Copyright © 2008 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3371-df4250f08c78cab082923f85a64c66825e1f4f7b642d3bccd2603862ef57262f3</citedby><cites>FETCH-LOGICAL-c3371-df4250f08c78cab082923f85a64c66825e1f4f7b642d3bccd2603862ef57262f3</cites></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>Narasimhulu, M.</creatorcontrib><creatorcontrib>Reddy, S. Malla</creatorcontrib><creatorcontrib>Rajesh, K.</creatorcontrib><creatorcontrib>Suryakiran, N.</creatorcontrib><creatorcontrib>Ramesh, D.</creatorcontrib><creatorcontrib>Venkateswarlu, Y.</creatorcontrib><title>A mild and efficient synthesis of chiral tetrahydroquinolino pyranose derivatives catalyzed by lanthanum(iii) nitrate hexahydrate</title><title>Heteroatom chemistry</title><addtitle>Heteroatom Chem</addtitle><description>A mild and highly efficient synthesis of chiral tetrahydroquinolino pyranose derivatives is described. The reaction of a chiral α,β‐unsaturated aldehyde containing a hydroxyl group with different aryl amines using lanthanum(III) nitrate hexahydrate as a catalyst afforded corresponding chiral tetrahydroquinolinated pyranosides in excellent yields. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:429–433, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20441</description><issn>1042-7163</issn><issn>1098-1071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kLtOwzAARSMEEqUg8Qkey5DiV2x3rCpoQeUhAYLNch1bMaRJsd3SsPHnpC1iQGK4unc4OsNNklME-whCfF7oPoaUor2kg-BApAhytL_ZFKccMXKYHIXwCiFCdCA6ydcQzF2ZA1XlwFjrtDNVBKGpYmGCC6C2QBfOqxJEE70qmtzX70tX1WUbsGi8qupgQG68W6noViYAraIqm0-Tg1kDStWaVLWc95xzZ6ByrSQaUJj11tXu4-TAqjKYk5_uJk-XF4-jSTq9G1-NhtNUE8JRmluKM2ih0FxoNYMCDzCxIlOMasYEzgyy1PIZozgnM61zzCARDBubccywJd2kt_NqX4fgjZUL7-bKNxJBublOFlpur2vRdId-uNI0_3JyMvrDuxDN-pdX_k0yTngmn2_HktJ7fn2TvcgH8g17LYEY</recordid><startdate>200805</startdate><enddate>200805</enddate><creator>Narasimhulu, M.</creator><creator>Reddy, S. Malla</creator><creator>Rajesh, K.</creator><creator>Suryakiran, N.</creator><creator>Ramesh, D.</creator><creator>Venkateswarlu, Y.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200805</creationdate><title>A mild and efficient synthesis of chiral tetrahydroquinolino pyranose derivatives catalyzed by lanthanum(iii) nitrate hexahydrate</title><author>Narasimhulu, M. ; Reddy, S. Malla ; Rajesh, K. ; Suryakiran, N. ; Ramesh, D. ; Venkateswarlu, Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3371-df4250f08c78cab082923f85a64c66825e1f4f7b642d3bccd2603862ef57262f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Narasimhulu, M.</creatorcontrib><creatorcontrib>Reddy, S. Malla</creatorcontrib><creatorcontrib>Rajesh, K.</creatorcontrib><creatorcontrib>Suryakiran, N.</creatorcontrib><creatorcontrib>Ramesh, D.</creatorcontrib><creatorcontrib>Venkateswarlu, Y.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Heteroatom chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Narasimhulu, M.</au><au>Reddy, S. Malla</au><au>Rajesh, K.</au><au>Suryakiran, N.</au><au>Ramesh, D.</au><au>Venkateswarlu, Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A mild and efficient synthesis of chiral tetrahydroquinolino pyranose derivatives catalyzed by lanthanum(iii) nitrate hexahydrate</atitle><jtitle>Heteroatom chemistry</jtitle><addtitle>Heteroatom Chem</addtitle><date>2008-05</date><risdate>2008</risdate><volume>19</volume><issue>4</issue><spage>429</spage><epage>433</epage><pages>429-433</pages><issn>1042-7163</issn><eissn>1098-1071</eissn><abstract>A mild and highly efficient synthesis of chiral tetrahydroquinolino pyranose derivatives is described. The reaction of a chiral α,β‐unsaturated aldehyde containing a hydroxyl group with different aryl amines using lanthanum(III) nitrate hexahydrate as a catalyst afforded corresponding chiral tetrahydroquinolinated pyranosides in excellent yields. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:429–433, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20441</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/hc.20441</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1042-7163 |
| ispartof | Heteroatom chemistry, 2008-05, Vol.19 (4), p.429-433 |
| issn | 1042-7163 1098-1071 |
| language | eng |
| recordid | cdi_crossref_primary_10_1002_hc_20441 |
| source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
| title | A mild and efficient synthesis of chiral tetrahydroquinolino pyranose derivatives catalyzed by lanthanum(iii) nitrate hexahydrate |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T08%3A32%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20mild%20and%20efficient%20synthesis%20of%20chiral%20tetrahydroquinolino%20pyranose%20derivatives%20catalyzed%20by%20lanthanum(iii)%20nitrate%20hexahydrate&rft.jtitle=Heteroatom%20chemistry&rft.au=Narasimhulu,%20M.&rft.date=2008-05&rft.volume=19&rft.issue=4&rft.spage=429&rft.epage=433&rft.pages=429-433&rft.issn=1042-7163&rft.eissn=1098-1071&rft_id=info:doi/10.1002/hc.20441&rft_dat=%3Cistex_cross%3Eark_67375_WNG_44P7JM5X_S%3C/istex_cross%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 |