Reactions of benzazole-2-thiones with 3,5-di-tert-butyl-4-hydroxybenzyl acetate
The benzylation of benzothiazole(oxazole, imidazole)-2-thiones with 3,5-di- tert -butyl-4-hydroxybenzyl acetate involves either the sulfur or nitrogen atom depending on the reaction conditions. The S - and N -benzylation products of benzazole-2-thiones are kinetically and thermodynamically controlle...
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Veröffentlicht in: | Russian journal of general chemistry 2017, Vol.87 (1), p.22-28 |
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container_title | Russian journal of general chemistry |
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creator | Tagasheva, R. G. Gataullina, D. R. Zaripova, I. F. Bukharov, S. V. Nugumanova, G. N. Deberdeev, T. R. Voronina, Yu. K. |
description | The benzylation of benzothiazole(oxazole, imidazole)-2-thiones with 3,5-di-
tert
-butyl-4-hydroxybenzyl acetate involves either the sulfur or nitrogen atom depending on the reaction conditions. The
S
- and
N
-benzylation products of benzazole-2-thiones are kinetically and thermodynamically controlled products, respectively. The use of 3,5-di-
tert
-butyl-4-hydroxy-benzyl acetate allows sterically hindered hydroxybenzyl derivatives of benzаzole-2-thiones to be generally synthesized under milder conditions than in known methods of their synthesis. |
doi_str_mv | 10.1134/S1070363217010054 |
format | Article |
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tert
-butyl-4-hydroxybenzyl acetate involves either the sulfur or nitrogen atom depending on the reaction conditions. The
S
- and
N
-benzylation products of benzazole-2-thiones are kinetically and thermodynamically controlled products, respectively. The use of 3,5-di-
tert
-butyl-4-hydroxy-benzyl acetate allows sterically hindered hydroxybenzyl derivatives of benzаzole-2-thiones to be generally synthesized under milder conditions than in known methods of their synthesis.</description><identifier>ISSN: 1070-3632</identifier><identifier>EISSN: 1608-3350</identifier><identifier>DOI: 10.1134/S1070363217010054</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Imidazole ; Oxazole</subject><ispartof>Russian journal of general chemistry, 2017, Vol.87 (1), p.22-28</ispartof><rights>Pleiades Publishing, Ltd. 2017</rights><rights>Copyright Springer Science & Business Media 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-411c8abac80c1f6c15f4897e10a185b133121f9722cc215a6ff78312bef393513</citedby><cites>FETCH-LOGICAL-c316t-411c8abac80c1f6c15f4897e10a185b133121f9722cc215a6ff78312bef393513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1070363217010054$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1070363217010054$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51298</link.rule.ids></links><search><creatorcontrib>Tagasheva, R. G.</creatorcontrib><creatorcontrib>Gataullina, D. R.</creatorcontrib><creatorcontrib>Zaripova, I. F.</creatorcontrib><creatorcontrib>Bukharov, S. V.</creatorcontrib><creatorcontrib>Nugumanova, G. N.</creatorcontrib><creatorcontrib>Deberdeev, T. R.</creatorcontrib><creatorcontrib>Voronina, Yu. K.</creatorcontrib><title>Reactions of benzazole-2-thiones with 3,5-di-tert-butyl-4-hydroxybenzyl acetate</title><title>Russian journal of general chemistry</title><addtitle>Russ J Gen Chem</addtitle><description>The benzylation of benzothiazole(oxazole, imidazole)-2-thiones with 3,5-di-
tert
-butyl-4-hydroxybenzyl acetate involves either the sulfur or nitrogen atom depending on the reaction conditions. The
S
- and
N
-benzylation products of benzazole-2-thiones are kinetically and thermodynamically controlled products, respectively. The use of 3,5-di-
tert
-butyl-4-hydroxy-benzyl acetate allows sterically hindered hydroxybenzyl derivatives of benzаzole-2-thiones to be generally synthesized under milder conditions than in known methods of their synthesis.</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Imidazole</subject><subject>Oxazole</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kM1LxDAQxYMouK7-Ad4KXo1mkqbNHmXxCxYW_DiXNDtxu9RmTVK0-9ebsh4E8TTDvN97A4-Qc2BXACK_fgZWMlEIDiUDxmR-QCZQMEWFkOww7Ummo35MTkLYsBEq-IQsn1Cb2LguZM5mNXY7vXMtUk7jOl0xZJ9NXGfiUtJVQyP6SOs-Di3N6XpYefc1jJ6hzbTBqCOekiOr24BnP3NKXu9uX-YPdLG8f5zfLKgRUESaAxila20UM2ALA9LmalYiMA1K1iAEcLCzknNjOEhdWFuqdKvRipmQIKbkYp-79e6jxxCrjet9l15WoBQrJVe5TBTsKeNdCB5ttfXNu_ZDBawae6v-9JY8fO8Jie3e0P9K_tf0DdJLbTI</recordid><startdate>2017</startdate><enddate>2017</enddate><creator>Tagasheva, R. G.</creator><creator>Gataullina, D. R.</creator><creator>Zaripova, I. F.</creator><creator>Bukharov, S. V.</creator><creator>Nugumanova, G. N.</creator><creator>Deberdeev, T. R.</creator><creator>Voronina, Yu. K.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2017</creationdate><title>Reactions of benzazole-2-thiones with 3,5-di-tert-butyl-4-hydroxybenzyl acetate</title><author>Tagasheva, R. G. ; Gataullina, D. R. ; Zaripova, I. F. ; Bukharov, S. V. ; Nugumanova, G. N. ; Deberdeev, T. R. ; Voronina, Yu. K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-411c8abac80c1f6c15f4897e10a185b133121f9722cc215a6ff78312bef393513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Imidazole</topic><topic>Oxazole</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tagasheva, R. G.</creatorcontrib><creatorcontrib>Gataullina, D. R.</creatorcontrib><creatorcontrib>Zaripova, I. F.</creatorcontrib><creatorcontrib>Bukharov, S. V.</creatorcontrib><creatorcontrib>Nugumanova, G. N.</creatorcontrib><creatorcontrib>Deberdeev, T. R.</creatorcontrib><creatorcontrib>Voronina, Yu. K.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tagasheva, R. G.</au><au>Gataullina, D. R.</au><au>Zaripova, I. F.</au><au>Bukharov, S. V.</au><au>Nugumanova, G. N.</au><au>Deberdeev, T. R.</au><au>Voronina, Yu. K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reactions of benzazole-2-thiones with 3,5-di-tert-butyl-4-hydroxybenzyl acetate</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2017</date><risdate>2017</risdate><volume>87</volume><issue>1</issue><spage>22</spage><epage>28</epage><pages>22-28</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>The benzylation of benzothiazole(oxazole, imidazole)-2-thiones with 3,5-di-
tert
-butyl-4-hydroxybenzyl acetate involves either the sulfur or nitrogen atom depending on the reaction conditions. The
S
- and
N
-benzylation products of benzazole-2-thiones are kinetically and thermodynamically controlled products, respectively. The use of 3,5-di-
tert
-butyl-4-hydroxy-benzyl acetate allows sterically hindered hydroxybenzyl derivatives of benzаzole-2-thiones to be generally synthesized under milder conditions than in known methods of their synthesis.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070363217010054</doi><tpages>7</tpages></addata></record> |
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subjects | Chemistry Chemistry and Materials Science Chemistry/Food Science Imidazole Oxazole |
title | Reactions of benzazole-2-thiones with 3,5-di-tert-butyl-4-hydroxybenzyl acetate |
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