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Dual Platinum and Pyrrolidine Catalysis in the Direct Alkylation of Allylic Alcohols: Selective Synthesis of Monoallylation Products
A dual platinum‐ and pyrrolidine‐catalyzed direct allylic alkylation of allylic alcohols with various active methylene compounds to produce products with high monoallylation selectivity was developed. The use of pyrrolidine and acetic acid was essential, not only for preventing undesirable side reac...
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Published in: | Angewandte Chemie International Edition 2014-04, Vol.53 (17), p.4377-4381 |
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creator | Shibuya, Ryozo Lin, Lu Nakahara, Yasuhito Mashima, Kazushi Ohshima, Takashi |
description | A dual platinum‐ and pyrrolidine‐catalyzed direct allylic alkylation of allylic alcohols with various active methylene compounds to produce products with high monoallylation selectivity was developed. The use of pyrrolidine and acetic acid was essential, not only for preventing undesirable side reactions, but also for obtaining high monoallylation selectivity.
Two cats are better than one: The combined use of platinum and pyrrolidine catalysts enabled the direct alkylation of allylic alcohols with reactive methylene compounds. Pyrrolidine was essential for obtaining high selectivity of the monoallylation products, which were produced without the use of excess nucleophiles. cod=1,5‐cyclooctadiene, EWG=electron‐withdrawing group. |
doi_str_mv | 10.1002/anie.201311200 |
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Two cats are better than one: The combined use of platinum and pyrrolidine catalysts enabled the direct alkylation of allylic alcohols with reactive methylene compounds. Pyrrolidine was essential for obtaining high selectivity of the monoallylation products, which were produced without the use of excess nucleophiles. cod=1,5‐cyclooctadiene, EWG=electron‐withdrawing group.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201311200</identifier><identifier>PMID: 24604875</identifier><identifier>CODEN: ACIEAY</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Acetic acid ; Alcohols ; Alkylation ; Allyl Compounds - chemical synthesis ; allylic alkylation ; Catalysis ; Cats ; homogeneous catalysis ; Methylene ; Molecular Structure ; Nucleophiles ; organocatalysis ; Platinum ; Platinum - chemistry ; Propanols - chemistry ; pyrrolidine ; Pyrrolidines - chemistry ; Selectivity ; Stereoisomerism</subject><ispartof>Angewandte Chemie International Edition, 2014-04, Vol.53 (17), p.4377-4381</ispartof><rights>2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5470-65d7cc0aa49eaa57c2193f15bc6da8627b1aacc7538b8e56476eb1eda1f370183</citedby><cites>FETCH-LOGICAL-c5470-65d7cc0aa49eaa57c2193f15bc6da8627b1aacc7538b8e56476eb1eda1f370183</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/24604875$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shibuya, Ryozo</creatorcontrib><creatorcontrib>Lin, Lu</creatorcontrib><creatorcontrib>Nakahara, Yasuhito</creatorcontrib><creatorcontrib>Mashima, Kazushi</creatorcontrib><creatorcontrib>Ohshima, Takashi</creatorcontrib><title>Dual Platinum and Pyrrolidine Catalysis in the Direct Alkylation of Allylic Alcohols: Selective Synthesis of Monoallylation Products</title><title>Angewandte Chemie International Edition</title><addtitle>Angew. Chem. Int. Ed</addtitle><description>A dual platinum‐ and pyrrolidine‐catalyzed direct allylic alkylation of allylic alcohols with various active methylene compounds to produce products with high monoallylation selectivity was developed. The use of pyrrolidine and acetic acid was essential, not only for preventing undesirable side reactions, but also for obtaining high monoallylation selectivity.
Two cats are better than one: The combined use of platinum and pyrrolidine catalysts enabled the direct alkylation of allylic alcohols with reactive methylene compounds. Pyrrolidine was essential for obtaining high selectivity of the monoallylation products, which were produced without the use of excess nucleophiles. cod=1,5‐cyclooctadiene, EWG=electron‐withdrawing group.</description><subject>Acetic acid</subject><subject>Alcohols</subject><subject>Alkylation</subject><subject>Allyl Compounds - chemical synthesis</subject><subject>allylic alkylation</subject><subject>Catalysis</subject><subject>Cats</subject><subject>homogeneous catalysis</subject><subject>Methylene</subject><subject>Molecular Structure</subject><subject>Nucleophiles</subject><subject>organocatalysis</subject><subject>Platinum</subject><subject>Platinum - chemistry</subject><subject>Propanols - chemistry</subject><subject>pyrrolidine</subject><subject>Pyrrolidines - chemistry</subject><subject>Selectivity</subject><subject>Stereoisomerism</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqN0Utv1DAUBeAIgWgpbFkiS2zYZPCNYzthN5rpS-qUkcprZzmOo7r12MVOaLPnh-MoZYTYwOra0neOZd0sew14ARgX76UzelFgIAAFxk-yQ6AF5IRz8jSdS0JyXlE4yF7EeJN8VWH2PDsoSobLitPD7Od6kBZtreyNG3ZIuhZtxxC8Na1xGq1kL-0YTUTGof5ao7UJWvVoaW_HKeMd8l262dEalaby197GD-hK28TMD42uRpdyU0OCG--8nPAc3QbfDqqPL7NnnbRRv3qcR9nnk-NPq7P84uPp-Wp5kStacpwz2nKlsJRlraWkXBVQkw5oo1grK1bwBqRUilNSNZWmrORMN6BbCR3hGCpylL2be--C_z7o2IudiUpbK532QxSQFAZg9X9QCulFIGWR6Nu_6I0fgksfmRQnrKoJSWoxKxV8jEF34i6YnQyjACymVYpplWK_yhR481g7NDvd7vnv3SVQz-DeWD3-o04sL8-P_yzP56yJvX7YZ2W4FYwTTsXXy1MB39ZnXzbrE7EhvwCtQrrA</recordid><startdate>20140422</startdate><enddate>20140422</enddate><creator>Shibuya, Ryozo</creator><creator>Lin, Lu</creator><creator>Nakahara, Yasuhito</creator><creator>Mashima, Kazushi</creator><creator>Ohshima, Takashi</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20140422</creationdate><title>Dual Platinum and Pyrrolidine Catalysis in the Direct Alkylation of Allylic Alcohols: Selective Synthesis of Monoallylation Products</title><author>Shibuya, Ryozo ; Lin, Lu ; Nakahara, Yasuhito ; Mashima, Kazushi ; Ohshima, Takashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5470-65d7cc0aa49eaa57c2193f15bc6da8627b1aacc7538b8e56476eb1eda1f370183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acetic acid</topic><topic>Alcohols</topic><topic>Alkylation</topic><topic>Allyl Compounds - chemical synthesis</topic><topic>allylic alkylation</topic><topic>Catalysis</topic><topic>Cats</topic><topic>homogeneous catalysis</topic><topic>Methylene</topic><topic>Molecular Structure</topic><topic>Nucleophiles</topic><topic>organocatalysis</topic><topic>Platinum</topic><topic>Platinum - chemistry</topic><topic>Propanols - chemistry</topic><topic>pyrrolidine</topic><topic>Pyrrolidines - chemistry</topic><topic>Selectivity</topic><topic>Stereoisomerism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shibuya, Ryozo</creatorcontrib><creatorcontrib>Lin, Lu</creatorcontrib><creatorcontrib>Nakahara, Yasuhito</creatorcontrib><creatorcontrib>Mashima, Kazushi</creatorcontrib><creatorcontrib>Ohshima, Takashi</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shibuya, Ryozo</au><au>Lin, Lu</au><au>Nakahara, Yasuhito</au><au>Mashima, Kazushi</au><au>Ohshima, Takashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dual Platinum and Pyrrolidine Catalysis in the Direct Alkylation of Allylic Alcohols: Selective Synthesis of Monoallylation Products</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew. Chem. Int. Ed</addtitle><date>2014-04-22</date><risdate>2014</risdate><volume>53</volume><issue>17</issue><spage>4377</spage><epage>4381</epage><pages>4377-4381</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><abstract>A dual platinum‐ and pyrrolidine‐catalyzed direct allylic alkylation of allylic alcohols with various active methylene compounds to produce products with high monoallylation selectivity was developed. The use of pyrrolidine and acetic acid was essential, not only for preventing undesirable side reactions, but also for obtaining high monoallylation selectivity.
Two cats are better than one: The combined use of platinum and pyrrolidine catalysts enabled the direct alkylation of allylic alcohols with reactive methylene compounds. Pyrrolidine was essential for obtaining high selectivity of the monoallylation products, which were produced without the use of excess nucleophiles. cod=1,5‐cyclooctadiene, EWG=electron‐withdrawing group.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>24604875</pmid><doi>10.1002/anie.201311200</doi><tpages>5</tpages><edition>International ed. in English</edition></addata></record> |
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subjects | Acetic acid Alcohols Alkylation Allyl Compounds - chemical synthesis allylic alkylation Catalysis Cats homogeneous catalysis Methylene Molecular Structure Nucleophiles organocatalysis Platinum Platinum - chemistry Propanols - chemistry pyrrolidine Pyrrolidines - chemistry Selectivity Stereoisomerism |
title | Dual Platinum and Pyrrolidine Catalysis in the Direct Alkylation of Allylic Alcohols: Selective Synthesis of Monoallylation Products |
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