Synthesis of polysubstituted 3,4-dihydro-2-thiopyrans by regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester
Polyfunctionalized 3,4-dihydro-2 H -thiopyrans were obtained in high yields via the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF 3 ·Et 2 O catalysis. Polyfunctionalized 3,4-dihydro-2 H -thiopyrans were obtained in high yields via the regioselective...
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Veröffentlicht in: | New journal of chemistry 2017-11, Vol.41 (22), p.13219-13221 |
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container_issue | 22 |
container_start_page | 13219 |
container_title | New journal of chemistry |
container_volume | 41 |
creator | Kurva, Srinivas Sriramoju, Vinodkumar Madabhushi, Sridhar Nanubolu, Jagadeesh Babu |
description | Polyfunctionalized 3,4-dihydro-2
H
-thiopyrans were obtained in high yields
via
the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF
3
·Et
2
O catalysis.
Polyfunctionalized 3,4-dihydro-2
H
-thiopyrans were obtained in high yields
via
the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF
3
·Et
2
O catalysis. |
doi_str_mv | 10.1039/c7nj03025h |
format | Article |
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H
-thiopyrans were obtained in high yields
via
the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF
3
·Et
2
O catalysis.
Polyfunctionalized 3,4-dihydro-2
H
-thiopyrans were obtained in high yields
via
the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF
3
·Et
2
O catalysis.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/c7nj03025h</identifier><ispartof>New journal of chemistry, 2017-11, Vol.41 (22), p.13219-13221</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Kurva, Srinivas</creatorcontrib><creatorcontrib>Sriramoju, Vinodkumar</creatorcontrib><creatorcontrib>Madabhushi, Sridhar</creatorcontrib><creatorcontrib>Nanubolu, Jagadeesh Babu</creatorcontrib><title>Synthesis of polysubstituted 3,4-dihydro-2-thiopyrans by regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester</title><title>New journal of chemistry</title><description>Polyfunctionalized 3,4-dihydro-2
H
-thiopyrans were obtained in high yields
via
the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF
3
·Et
2
O catalysis.
Polyfunctionalized 3,4-dihydro-2
H
-thiopyrans were obtained in high yields
via
the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF
3
·Et
2
O catalysis.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFj8FKAzEURYNYsFo37gv5gKYmk-mUWYvi3u5LmknNKzFvyMtU8xn-ih_iNzkFQXddnQuXe-AydqfkUknd3tt1PEgtq5W_YFOlm1a0VaMux6zqWshV3Vyxa6KDlEqtGzVlny8lZu8IiOOe9xgKDTvKkIfsOq4XtejAly6hqET2gH1JJhLfFZ7cKyC54GyGo-MmxiGYDBhPIr3Q4_C_yoRQAtiRFj0G4u-QPTf8-0vgB3ZwkjvKLs3YZG8Cudtf3rD50-Pm4Vkksts-wZtJZfv3U5_rfwD8q1q8</recordid><startdate>20171106</startdate><enddate>20171106</enddate><creator>Kurva, Srinivas</creator><creator>Sriramoju, Vinodkumar</creator><creator>Madabhushi, Sridhar</creator><creator>Nanubolu, Jagadeesh Babu</creator><scope/></search><sort><creationdate>20171106</creationdate><title>Synthesis of polysubstituted 3,4-dihydro-2-thiopyrans by regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester</title><author>Kurva, Srinivas ; Sriramoju, Vinodkumar ; Madabhushi, Sridhar ; Nanubolu, Jagadeesh Babu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c7nj03025h3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kurva, Srinivas</creatorcontrib><creatorcontrib>Sriramoju, Vinodkumar</creatorcontrib><creatorcontrib>Madabhushi, Sridhar</creatorcontrib><creatorcontrib>Nanubolu, Jagadeesh Babu</creatorcontrib><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kurva, Srinivas</au><au>Sriramoju, Vinodkumar</au><au>Madabhushi, Sridhar</au><au>Nanubolu, Jagadeesh Babu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of polysubstituted 3,4-dihydro-2-thiopyrans by regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester</atitle><jtitle>New journal of chemistry</jtitle><date>2017-11-06</date><risdate>2017</risdate><volume>41</volume><issue>22</issue><spage>13219</spage><epage>13221</epage><pages>13219-13221</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>Polyfunctionalized 3,4-dihydro-2
H
-thiopyrans were obtained in high yields
via
the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF
3
·Et
2
O catalysis.
Polyfunctionalized 3,4-dihydro-2
H
-thiopyrans were obtained in high yields
via
the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF
3
·Et
2
O catalysis.</abstract><doi>10.1039/c7nj03025h</doi><tpages>3</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals; Alma/SFX Local Collection |
title | Synthesis of polysubstituted 3,4-dihydro-2-thiopyrans by regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester |
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