Stereoselective Synthesis of 2,4-Disubstituted Thiochromans Using the Supported Reagent System ‘Na2CO3/SiO2-PPA/SiO2’
Abstract A simple and efficient method has been developed for the stereoselective synthesis of 2,4-disubstituted thiochromans from arylthiols and α,β-unsaturated aldehydes by using an acid- and a base-supported reagent system, Na 2 CO 3 /SiO 2 -PPA/SiO 2 . Michael addition of arylthiol to α,β-unsatu...
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Veröffentlicht in: | Synlett 2007-02, Vol.2007 (3), p.0387-0390 |
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container_issue | 3 |
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container_title | Synlett |
container_volume | 2007 |
creator | Aoyama, Tadashi Okada, Kazuyuki Nakajima, Hideaki Matsumoto, Takuo Takido, Toshio Kodomari, Mitsuo |
description | Abstract
A simple and efficient method has been developed for the stereoselective synthesis of 2,4-disubstituted thiochromans from arylthiols and α,β-unsaturated aldehydes by using an acid- and a base-supported reagent system, Na
2
CO
3
/SiO
2
-PPA/SiO
2
. Michael addition of arylthiol to α,β-unsaturated aldehydes was promoted by Na
2
CO
3
/SiO
2
, and then the product was cyclized in the presence of PPA/SiO
2
. |
doi_str_mv | 10.1055/s-2007-967935 |
format | Article |
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A simple and efficient method has been developed for the stereoselective synthesis of 2,4-disubstituted thiochromans from arylthiols and α,β-unsaturated aldehydes by using an acid- and a base-supported reagent system, Na
2
CO
3
/SiO
2
-PPA/SiO
2
. Michael addition of arylthiol to α,β-unsaturated aldehydes was promoted by Na
2
CO
3
/SiO
2
, and then the product was cyclized in the presence of PPA/SiO
2
.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-2007-967935</identifier><language>eng ; jpn</language><subject>letter</subject><ispartof>Synlett, 2007-02, Vol.2007 (3), p.0387-0390</ispartof><rights>Georg Thieme Verlag Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2007-967935.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2007-967935$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3005,27901,27902,54534,54535</link.rule.ids></links><search><creatorcontrib>Aoyama, Tadashi</creatorcontrib><creatorcontrib>Okada, Kazuyuki</creatorcontrib><creatorcontrib>Nakajima, Hideaki</creatorcontrib><creatorcontrib>Matsumoto, Takuo</creatorcontrib><creatorcontrib>Takido, Toshio</creatorcontrib><creatorcontrib>Kodomari, Mitsuo</creatorcontrib><title>Stereoselective Synthesis of 2,4-Disubstituted Thiochromans Using the Supported Reagent System ‘Na2CO3/SiO2-PPA/SiO2’</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract
A simple and efficient method has been developed for the stereoselective synthesis of 2,4-disubstituted thiochromans from arylthiols and α,β-unsaturated aldehydes by using an acid- and a base-supported reagent system, Na
2
CO
3
/SiO
2
-PPA/SiO
2
. Michael addition of arylthiol to α,β-unsaturated aldehydes was promoted by Na
2
CO
3
/SiO
2
, and then the product was cyclized in the presence of PPA/SiO
2
.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNotkEtKA0EYhBtRMEaX7vsAadPvnl6G-IRggpOsh3n8yXRIZsJ0jyBucgw9hJfwKDmJE3VVRVFUwYfQNaM3jCo19IRTaojVxgp1gnpMCtNFVp-iHrVCE8WZPEcX3q8pZTKytIfe4wAN1B42kAf3Cjh-q0IJ3nlcLzEfSHLrfJv54EIboMDz0tV52dTbtPJ44V21wl0df3_F7W5XN8fKC6QrqEK35ANs8WH_8Zzy8VQMYzflZDYb_ZrD_vMSnS3TjYerf-2jxf3dfPxIJtOHp_FoQtbMCEWkVlSYCArLrRGFhhRUkfJC5VEeZUyDzCnXS1UIMEIKqzjPUyMgy6jOQCnRR4O_3VA62EKyrtum6g4TRpMjuMQnR3DJHzjxA0yGY0M</recordid><startdate>20070215</startdate><enddate>20070215</enddate><creator>Aoyama, Tadashi</creator><creator>Okada, Kazuyuki</creator><creator>Nakajima, Hideaki</creator><creator>Matsumoto, Takuo</creator><creator>Takido, Toshio</creator><creator>Kodomari, Mitsuo</creator><scope/></search><sort><creationdate>20070215</creationdate><title>Stereoselective Synthesis of 2,4-Disubstituted Thiochromans Using the Supported Reagent System ‘Na2CO3/SiO2-PPA/SiO2’</title><author>Aoyama, Tadashi ; Okada, Kazuyuki ; Nakajima, Hideaki ; Matsumoto, Takuo ; Takido, Toshio ; Kodomari, Mitsuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j1735-4650378ed92973d6eae5da2d5c8c8b16e4c026f5d3e73439522ca73ebb06be553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; jpn</language><creationdate>2007</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aoyama, Tadashi</creatorcontrib><creatorcontrib>Okada, Kazuyuki</creatorcontrib><creatorcontrib>Nakajima, Hideaki</creatorcontrib><creatorcontrib>Matsumoto, Takuo</creatorcontrib><creatorcontrib>Takido, Toshio</creatorcontrib><creatorcontrib>Kodomari, Mitsuo</creatorcontrib><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aoyama, Tadashi</au><au>Okada, Kazuyuki</au><au>Nakajima, Hideaki</au><au>Matsumoto, Takuo</au><au>Takido, Toshio</au><au>Kodomari, Mitsuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stereoselective Synthesis of 2,4-Disubstituted Thiochromans Using the Supported Reagent System ‘Na2CO3/SiO2-PPA/SiO2’</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2007-02-15</date><risdate>2007</risdate><volume>2007</volume><issue>3</issue><spage>0387</spage><epage>0390</epage><pages>0387-0390</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
A simple and efficient method has been developed for the stereoselective synthesis of 2,4-disubstituted thiochromans from arylthiols and α,β-unsaturated aldehydes by using an acid- and a base-supported reagent system, Na
2
CO
3
/SiO
2
-PPA/SiO
2
. Michael addition of arylthiol to α,β-unsaturated aldehydes was promoted by Na
2
CO
3
/SiO
2
, and then the product was cyclized in the presence of PPA/SiO
2
.</abstract><doi>10.1055/s-2007-967935</doi><tpages>4</tpages></addata></record> |
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issn | 0936-5214 1437-2096 |
language | eng ; jpn |
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source | Thieme Connect Journals |
subjects | letter |
title | Stereoselective Synthesis of 2,4-Disubstituted Thiochromans Using the Supported Reagent System ‘Na2CO3/SiO2-PPA/SiO2’ |
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