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Asymmetric Brønsted Acid Catalyzed Substitution of Diaryl Methanols with Thiols and Alcohols for the Synthesis of Chiral Thioethers and Ethers
An enantioselective addition of thiols and alcohols to aza‐ortho‐quinone methides, starting from diaryl methanols, was developed. The asymmetric additions occur under mild reaction conditions in the presence of chiral phosphoric acids and furnish the corresponding adducts with excellent yields and e...
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Published in: | Angewandte Chemie International Edition 2016-04, Vol.55 (15), p.4803-4807 |
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container_title | Angewandte Chemie International Edition |
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creator | Chatupheeraphat, Adisak Liao, Hsuan-Hung Mader, Steffen Sako, Makoto Sasai, Hiroaki Atodiresei, Iuliana Rueping, Magnus |
description | An enantioselective addition of thiols and alcohols to aza‐ortho‐quinone methides, starting from diaryl methanols, was developed. The asymmetric additions occur under mild reaction conditions in the presence of chiral phosphoric acids and furnish the corresponding adducts with excellent yields and enantioselectivities.
Take two: An enantioselective addition of thiols and alcohols to aza‐ortho‐quinone methides, starting from diaryl methanols, has been developed. The asymmetric oxa‐ and sulfa‐Michael additions proceed under mild reaction conditions in the presence of chiral phosphoric acids to furnish the corresponding adducts with excellent yields and enantioselectivities. |
doi_str_mv | 10.1002/anie.201511179 |
format | article |
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Take two: An enantioselective addition of thiols and alcohols to aza‐ortho‐quinone methides, starting from diaryl methanols, has been developed. The asymmetric oxa‐ and sulfa‐Michael additions proceed under mild reaction conditions in the presence of chiral phosphoric acids to furnish the corresponding adducts with excellent yields and enantioselectivities.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201511179</identifier><identifier>PMID: 26952288</identifier><identifier>CODEN: ACIEAY</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Acids ; Adducts ; Alcohol ; Alcohols ; Asymmetry ; Brønsted acids ; carbenium ions ; Enantiomers ; Ethers ; Michael addition ; ortho-quinone methides ; Quinones ; substitution ; Thioethers ; Thiols</subject><ispartof>Angewandte Chemie International Edition, 2016-04, Vol.55 (15), p.4803-4807</ispartof><rights>2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4769-e09634bcb2c7f3757818c6ed571fdc6af2cdec15eb2b3fff13497c419868b7b3</citedby><cites>FETCH-LOGICAL-c4769-e09634bcb2c7f3757818c6ed571fdc6af2cdec15eb2b3fff13497c419868b7b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26952288$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chatupheeraphat, Adisak</creatorcontrib><creatorcontrib>Liao, Hsuan-Hung</creatorcontrib><creatorcontrib>Mader, Steffen</creatorcontrib><creatorcontrib>Sako, Makoto</creatorcontrib><creatorcontrib>Sasai, Hiroaki</creatorcontrib><creatorcontrib>Atodiresei, Iuliana</creatorcontrib><creatorcontrib>Rueping, Magnus</creatorcontrib><title>Asymmetric Brønsted Acid Catalyzed Substitution of Diaryl Methanols with Thiols and Alcohols for the Synthesis of Chiral Thioethers and Ethers</title><title>Angewandte Chemie International Edition</title><addtitle>Angew. Chem. Int. Ed</addtitle><description>An enantioselective addition of thiols and alcohols to aza‐ortho‐quinone methides, starting from diaryl methanols, was developed. The asymmetric additions occur under mild reaction conditions in the presence of chiral phosphoric acids and furnish the corresponding adducts with excellent yields and enantioselectivities.
Take two: An enantioselective addition of thiols and alcohols to aza‐ortho‐quinone methides, starting from diaryl methanols, has been developed. The asymmetric oxa‐ and sulfa‐Michael additions proceed under mild reaction conditions in the presence of chiral phosphoric acids to furnish the corresponding adducts with excellent yields and enantioselectivities.</description><subject>Acids</subject><subject>Adducts</subject><subject>Alcohol</subject><subject>Alcohols</subject><subject>Asymmetry</subject><subject>Brønsted acids</subject><subject>carbenium ions</subject><subject>Enantiomers</subject><subject>Ethers</subject><subject>Michael addition</subject><subject>ortho-quinone methides</subject><subject>Quinones</subject><subject>substitution</subject><subject>Thioethers</subject><subject>Thiols</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkUtv1DAUhSMEog_YskSW2LDJ4EdiO8vpMPShMqjqCJaW49iKSx6t7aikf4K_w75_rE5TRogFeHPvkb5zZN2TJG8QXCAI8QfZWb3AEOUIIVY8S_ZRjlFKGCPP454RkjKeo73kwPuryHMO6ctkD9Mix1HsJz-XfmxbHZxV4Mjd_-p80BVYKluBlQyyGe-ivBxKH2wYgu070Bvw0Uo3NuCzDrXs-saDWxtqsK3ttMsu-hvV15MwvQOh1uBy7OLw1k_2VW2dbB75mKDd7Fk_rq-SF0Y2Xr9-mofJ9tN6uzpJz78cn66W56nKGC1SDQtKslKVWDFDWM444orqKmfIVIpKg1WlFcp1iUtijEEkK5jKUMEpL1lJDpP3c-y1628G7YNorVe6aWSn-8ELxBjPIMwYjOi7v9CrfnBd_JxABaQUQorJPykWH0U445FazJRyvfdOG3HtbBuPKRAUU59i6lPs-oyGt0-xQ9nqaof_LjACxQzc2kaP_4kTy83p-s_wdPbaWPqPnVe674KyeFTxbXMsLo74GWZfL8SGPADjyb1Y</recordid><startdate>20160404</startdate><enddate>20160404</enddate><creator>Chatupheeraphat, Adisak</creator><creator>Liao, Hsuan-Hung</creator><creator>Mader, Steffen</creator><creator>Sako, Makoto</creator><creator>Sasai, Hiroaki</creator><creator>Atodiresei, Iuliana</creator><creator>Rueping, Magnus</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20160404</creationdate><title>Asymmetric Brønsted Acid Catalyzed Substitution of Diaryl Methanols with Thiols and Alcohols for the Synthesis of Chiral Thioethers and Ethers</title><author>Chatupheeraphat, Adisak ; Liao, Hsuan-Hung ; Mader, Steffen ; Sako, Makoto ; Sasai, Hiroaki ; Atodiresei, Iuliana ; Rueping, Magnus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4769-e09634bcb2c7f3757818c6ed571fdc6af2cdec15eb2b3fff13497c419868b7b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acids</topic><topic>Adducts</topic><topic>Alcohol</topic><topic>Alcohols</topic><topic>Asymmetry</topic><topic>Brønsted acids</topic><topic>carbenium ions</topic><topic>Enantiomers</topic><topic>Ethers</topic><topic>Michael addition</topic><topic>ortho-quinone methides</topic><topic>Quinones</topic><topic>substitution</topic><topic>Thioethers</topic><topic>Thiols</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chatupheeraphat, Adisak</creatorcontrib><creatorcontrib>Liao, Hsuan-Hung</creatorcontrib><creatorcontrib>Mader, Steffen</creatorcontrib><creatorcontrib>Sako, Makoto</creatorcontrib><creatorcontrib>Sasai, Hiroaki</creatorcontrib><creatorcontrib>Atodiresei, Iuliana</creatorcontrib><creatorcontrib>Rueping, Magnus</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chatupheeraphat, Adisak</au><au>Liao, Hsuan-Hung</au><au>Mader, Steffen</au><au>Sako, Makoto</au><au>Sasai, Hiroaki</au><au>Atodiresei, Iuliana</au><au>Rueping, Magnus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Asymmetric Brønsted Acid Catalyzed Substitution of Diaryl Methanols with Thiols and Alcohols for the Synthesis of Chiral Thioethers and Ethers</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew. Chem. Int. Ed</addtitle><date>2016-04-04</date><risdate>2016</risdate><volume>55</volume><issue>15</issue><spage>4803</spage><epage>4807</epage><pages>4803-4807</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><abstract>An enantioselective addition of thiols and alcohols to aza‐ortho‐quinone methides, starting from diaryl methanols, was developed. The asymmetric additions occur under mild reaction conditions in the presence of chiral phosphoric acids and furnish the corresponding adducts with excellent yields and enantioselectivities.
Take two: An enantioselective addition of thiols and alcohols to aza‐ortho‐quinone methides, starting from diaryl methanols, has been developed. The asymmetric oxa‐ and sulfa‐Michael additions proceed under mild reaction conditions in the presence of chiral phosphoric acids to furnish the corresponding adducts with excellent yields and enantioselectivities.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>26952288</pmid><doi>10.1002/anie.201511179</doi><tpages>5</tpages><edition>International ed. in English</edition></addata></record> |
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subjects | Acids Adducts Alcohol Alcohols Asymmetry Brønsted acids carbenium ions Enantiomers Ethers Michael addition ortho-quinone methides Quinones substitution Thioethers Thiols |
title | Asymmetric Brønsted Acid Catalyzed Substitution of Diaryl Methanols with Thiols and Alcohols for the Synthesis of Chiral Thioethers and Ethers |
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