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Ceric Ammonium Nitrate Catalyzed Oxidation of Aldehydes and Alcohols
A variety of aromatic, aliphatic and conjugated aldehydes and alcohols were transformed to the corresponding carboxylic acids and ketones with a quantitative conversion in high yields with 70% t-BuOOH solution in water in the presence of catalytic amounts of ceric ammonium nitrate [Ce(NH4)2(NO3)6] (...
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Published in: | Chinese journal of chemistry 2011-11, Vol.29 (11), p.2379-2384 |
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container_title | Chinese journal of chemistry |
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creator | Gowda, Ravikumar R. Chakraborty, Debashis |
description | A variety of aromatic, aliphatic and conjugated aldehydes and alcohols were transformed to the corresponding carboxylic acids and ketones with a quantitative conversion in high yields with 70% t-BuOOH solution in water in the presence of catalytic amounts of ceric ammonium nitrate [Ce(NH4)2(NO3)6] (CAN) under room temperature conditions. The scope of our catalytic system is applicable for a wide range of aromatic, conjugated and aliphatic substrates. These aldehydes were converted to the corresponding carboxylic acids in good isolated yields in reason- able times. This method possesses a wide range of capabilities since it can be used with other functional groups which may not tolerate oxidative conditions, involves fairly simple method for work-up, exhibits chemoselectivity and proceeds under ambient conditions. The resulting products are obtained in good yields within reasonable time. |
doi_str_mv | 10.1002/cjoc.201180406 |
format | article |
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Chakraborty, Debashis</creator><creatorcontrib>Gowda, Ravikumar R. Chakraborty, Debashis</creatorcontrib><description>A variety of aromatic, aliphatic and conjugated aldehydes and alcohols were transformed to the corresponding carboxylic acids and ketones with a quantitative conversion in high yields with 70% t-BuOOH solution in water in the presence of catalytic amounts of ceric ammonium nitrate [Ce(NH4)2(NO3)6] (CAN) under room temperature conditions. The scope of our catalytic system is applicable for a wide range of aromatic, conjugated and aliphatic substrates. These aldehydes were converted to the corresponding carboxylic acids in good isolated yields in reason- able times. This method possesses a wide range of capabilities since it can be used with other functional groups which may not tolerate oxidative conditions, involves fairly simple method for work-up, exhibits chemoselectivity and proceeds under ambient conditions. The resulting products are obtained in good yields within reasonable time.</description><identifier>ISSN: 1001-604X</identifier><identifier>EISSN: 1614-7065</identifier><identifier>DOI: 10.1002/cjoc.201180406</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Alcohol ; aldehyde ; ceric ammonium nitrate (CAN) ; oxidation ; t-BuOOH ; 催化体系 ; 催化氧化 ; 催化转化 ; 化学选择性 ; 室温条件 ; 硝酸铈铵 ; 醇 ; 醛</subject><ispartof>Chinese journal of chemistry, 2011-11, Vol.29 (11), p.2379-2384</ispartof><rights>Copyright © 2011 SIOC, CAS, Shanghai & WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2011 SIOC, CAS, Shanghai & WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3816-6890dc92f3e13cd47f76a9dd770ec5434842ddf89730c5307008b058078539ee3</citedby><cites>FETCH-LOGICAL-c3816-6890dc92f3e13cd47f76a9dd770ec5434842ddf89730c5307008b058078539ee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84126X/84126X.jpg</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Gowda, Ravikumar R. 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This method possesses a wide range of capabilities since it can be used with other functional groups which may not tolerate oxidative conditions, involves fairly simple method for work-up, exhibits chemoselectivity and proceeds under ambient conditions. The resulting products are obtained in good yields within reasonable time.</description><subject>Alcohol</subject><subject>aldehyde</subject><subject>ceric ammonium nitrate (CAN)</subject><subject>oxidation</subject><subject>t-BuOOH</subject><subject>催化体系</subject><subject>催化氧化</subject><subject>催化转化</subject><subject>化学选择性</subject><subject>室温条件</subject><subject>硝酸铈铵</subject><subject>醇</subject><subject>醛</subject><issn>1001-604X</issn><issn>1614-7065</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkN9LwzAQx4soOKevPld87rw0bZI-zuqmMjbw5_AlxCR1mV2zJR1u_vV2bAzfhMDl4PO5O75BcI6ggwDiKzm1shMDQgwSIAdBCxGURBRIetj8AVBEIBkfByfeTxue0pi0gptcOyPD7mxmK7OchUNTO1HrMBe1KNc_WoWjlVGiNrYKbRF2S6Una6V9KCrVdNJObOlPg6NClF6f7Wo7eOndPud30WDUv8-7g0hihkhEWAZKZnGBNcJSJbSgRGRKUQpapglOWBIrVbCMYpApBgrAPiBlQFmKM61xO7jczp07u1hqX_OpXbqqWckRJYRB87KG6mwp6az3Thd87sxMuDVHwDdJ8U1SfJ9UI2Rb4duUev0PzfOHUf7Xjbau8bVe7V3hvjihmKb8bdjn48dr8j7sPfHXhr_YHTex1efCVJ97JwHEUshS_AvkVoWn</recordid><startdate>201111</startdate><enddate>201111</enddate><creator>Gowda, Ravikumar R. Chakraborty, Debashis</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>~WA</scope><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201111</creationdate><title>Ceric Ammonium Nitrate Catalyzed Oxidation of Aldehydes and Alcohols</title><author>Gowda, Ravikumar R. 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Chakraborty, Debashis</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>维普中文期刊数据库</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Istex</collection><collection>CrossRef</collection><jtitle>Chinese journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gowda, Ravikumar R. 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These aldehydes were converted to the corresponding carboxylic acids in good isolated yields in reason- able times. This method possesses a wide range of capabilities since it can be used with other functional groups which may not tolerate oxidative conditions, involves fairly simple method for work-up, exhibits chemoselectivity and proceeds under ambient conditions. The resulting products are obtained in good yields within reasonable time.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/cjoc.201180406</doi><tpages>6</tpages></addata></record> |
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subjects | Alcohol aldehyde ceric ammonium nitrate (CAN) oxidation t-BuOOH 催化体系 催化氧化 催化转化 化学选择性 室温条件 硝酸铈铵 醇 醛 |
title | Ceric Ammonium Nitrate Catalyzed Oxidation of Aldehydes and Alcohols |
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