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Article: Reengineering Classic Organic Reactions Using Polymeric Tools

TitleReengineering Classic Organic Reactions Using Polymeric Tools
Authors
Issue Date2014
PublisherWalter de Gruyter GmbH. The Journal's web site is located at http://www.degruyter.com/view/j/pac
Citation
Pure and Applied Chemistry, 2014, v. 86 n. 11, p. 1651-1661 How to Cite?
AbstractMany of the most widely used reactions in organic synthesis suffer from drawbacks that can hamper their use. For example, the Mitsunobu, Wittig and Appel reactions all result in the formation of a full equivalent of triphenylphosphine oxide, which can be similar in polarity to the desired product, and thus be difficult to remove. Other reactions such as the Suzuki-Miyaura and Mizoroki-Heck reactions require the addition of numerous reagents, ligands and catalysts that can be laborious to separate from the targeted cross-coupled product. This review summarizes our recent work to address these issues by developing polymeric tools designed to simplify product isolation from these transformations.
DescriptionPaper based on presentation at the 15th International Conference on Polymers and Organic Chemistry (POC-2014), Timisoara, Romania, 10–13 June 2014
Persistent Identifierhttp://hdl.handle.net/10722/215156
ISSN
2015 Impact Factor: 2.615
2015 SCImago Journal Rankings: 0.912

 

DC FieldValueLanguage
dc.contributor.authorToy, PH-
dc.date.accessioned2015-08-21T13:16:23Z-
dc.date.available2015-08-21T13:16:23Z-
dc.date.issued2014-
dc.identifier.citationPure and Applied Chemistry, 2014, v. 86 n. 11, p. 1651-1661-
dc.identifier.issn0033-4545-
dc.identifier.urihttp://hdl.handle.net/10722/215156-
dc.descriptionPaper based on presentation at the 15th International Conference on Polymers and Organic Chemistry (POC-2014), Timisoara, Romania, 10–13 June 2014-
dc.description.abstractMany of the most widely used reactions in organic synthesis suffer from drawbacks that can hamper their use. For example, the Mitsunobu, Wittig and Appel reactions all result in the formation of a full equivalent of triphenylphosphine oxide, which can be similar in polarity to the desired product, and thus be difficult to remove. Other reactions such as the Suzuki-Miyaura and Mizoroki-Heck reactions require the addition of numerous reagents, ligands and catalysts that can be laborious to separate from the targeted cross-coupled product. This review summarizes our recent work to address these issues by developing polymeric tools designed to simplify product isolation from these transformations.-
dc.languageeng-
dc.publisherWalter de Gruyter GmbH. The Journal's web site is located at http://www.degruyter.com/view/j/pac-
dc.relation.ispartofPure and Applied Chemistry-
dc.rightsThe final publication is available at www.degruyter.com-
dc.rightsCreative Commons: Attribution 3.0 Hong Kong License-
dc.titleReengineering Classic Organic Reactions Using Polymeric Tools-
dc.typeArticle-
dc.identifier.emailToy, PH: phtoy@hkucc.hku.hk-
dc.identifier.authorityToy, PH=rp00791-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1515/pac-2014-0709-
dc.identifier.hkuros247802-
dc.identifier.volume86-
dc.identifier.issue11-
dc.identifier.spage1651-
dc.identifier.epage1661-
dc.publisher.placeGermany-

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