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Article: Organocatalytic highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes

TitleOrganocatalytic highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes
Authors
Issue Date2008
Citation
Organic Letters, 2008, v. 10, n. 13, p. 2817-2820 How to Cite?
Abstract(Chemical Equation Presented) The first organocatalytic enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes for the direct synthesis of chiral nitroalkylated naphthoquinone derivatives was investigated. Good yields and excellent enantioselectivities (up to >99% ee) could be achieved. This organocatalytic asymmetric Michael addition provides an efficient route torward the synthesis of optically active functionalized naphthoquinones. © 2008 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/291854
ISSN
2021 Impact Factor: 6.072
2020 SCImago Journal Rankings: 1.940
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhou, Wen Ming-
dc.contributor.authorLiu, Han-
dc.contributor.authorDu, Da Ming-
dc.date.accessioned2020-11-17T14:55:15Z-
dc.date.available2020-11-17T14:55:15Z-
dc.date.issued2008-
dc.identifier.citationOrganic Letters, 2008, v. 10, n. 13, p. 2817-2820-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/10722/291854-
dc.description.abstract(Chemical Equation Presented) The first organocatalytic enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes for the direct synthesis of chiral nitroalkylated naphthoquinone derivatives was investigated. Good yields and excellent enantioselectivities (up to >99% ee) could be achieved. This organocatalytic asymmetric Michael addition provides an efficient route torward the synthesis of optically active functionalized naphthoquinones. © 2008 American Chemical Society.-
dc.languageeng-
dc.relation.ispartofOrganic Letters-
dc.titleOrganocatalytic highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ol800945e-
dc.identifier.pmid18533672-
dc.identifier.scopuseid_2-s2.0-51649096678-
dc.identifier.volume10-
dc.identifier.issue13-
dc.identifier.spage2817-
dc.identifier.epage2820-
dc.identifier.isiWOS:000257211400051-
dc.identifier.issnl1523-7052-

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