Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100163
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorXiong, Ben_US
dc.creatorXu, Sen_US
dc.creatorZhu, Yen_US
dc.creatorYao, Len_US
dc.creatorZhou, Cen_US
dc.creatorLiu, Yen_US
dc.creatorTang, KWen_US
dc.creatorWong, WYen_US
dc.date.accessioned2023-08-08T01:52:42Z-
dc.date.available2023-08-08T01:52:42Z-
dc.identifier.issn0947-6539en_US
dc.identifier.urihttp://hdl.handle.net/10397/100163-
dc.language.isoenen_US
dc.publisherWiley-VCHen_US
dc.rights© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.rightsThis is the peer reviewed version of the following article: B. Xiong, S. Xu, Y. Zhu, L. Yao, C. Zhou, Y. Liu, K.-W. Tang, W.-Y. Wong, Metal-Free, N-Iodosuccinimide-Induced Regioselective Iodophosphoryloxylation of Alkenes with P(O)−OH Bonds. Chem. Eur. J. 2020, 26, 9556-9560, which has been published in final form at https://doi.org/10.1002/chem.202000575. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.en_US
dc.subjectAlkenesen_US
dc.subjectIodophosphoryloxylationen_US
dc.subjectPhosphorusen_US
dc.subjectSynthetic methodsen_US
dc.subjectTransition-metal-freeen_US
dc.titleMetal-free, N-iodosuccinimide-induced regioselective iodophosphoryloxylation of alkenes with P(O)−OH bondsen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationTitle in author's file: Metal-Free, NIS-Induced Regioselective Iodophosphoryloxylation of Alkenes with P(O)-OH bondsen_US
dc.identifier.spage9556en_US
dc.identifier.epage9560en_US
dc.identifier.volume26en_US
dc.identifier.issue43en_US
dc.identifier.doi10.1002/chem.202000575en_US
dcterms.abstractA simple and efficient method for the regioselective iodophosphoryloxylation of alkenes with P(O)−OH bonds has been established by using NIS (N-iodosuccinimide) as the iodination reagent under transition-metal-free conditions. The present protocol is compatible with different functional groups, and suitable for various alkenes and P(O)−OH compounds. A variety of functionalized β-iodo-1-ethyl phosphinic/phosphoric acid esters are obtained in good to excellent yields, which could be further transformed to diversified building blocks for the synthesis of bioactive compounds, pharmaceuticals and functional materials.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationChemistry - a European journal, 3 Aug. 2020, v. 26, no. 43, p. 9556-9560en_US
dcterms.isPartOfChemistry - a European journalen_US
dcterms.issued2020-08-03-
dc.identifier.scopus2-s2.0-85087611367-
dc.identifier.pmid32220090-
dc.identifier.eissn1521-3765en_US
dc.description.validate202308 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0280-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNSFC; Natural Science Foundation of Hunan Province; Scientific Research Fund of Hunan Provincial Education Department; Hunan Institute of Science and Technology; PolyU; Endowed Professorship in Energy from Ms Clarea Auen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS25505614-
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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