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- Publisher Website: 10.1021/ol800945e
- Scopus: eid_2-s2.0-51649096678
- PMID: 18533672
- WOS: WOS:000257211400051
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Article: Organocatalytic highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes
Title | Organocatalytic highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes |
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Authors | |
Issue Date | 2008 |
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 Identifier | http://hdl.handle.net/10722/291854 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.245 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Zhou, Wen Ming | - |
dc.contributor.author | Liu, Han | - |
dc.contributor.author | Du, Da Ming | - |
dc.date.accessioned | 2020-11-17T14:55:15Z | - |
dc.date.available | 2020-11-17T14:55:15Z | - |
dc.date.issued | 2008 | - |
dc.identifier.citation | Organic Letters, 2008, v. 10, n. 13, p. 2817-2820 | - |
dc.identifier.issn | 1523-7060 | - |
dc.identifier.uri | http://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.language | eng | - |
dc.relation.ispartof | Organic Letters | - |
dc.title | Organocatalytic highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/ol800945e | - |
dc.identifier.pmid | 18533672 | - |
dc.identifier.scopus | eid_2-s2.0-51649096678 | - |
dc.identifier.volume | 10 | - |
dc.identifier.issue | 13 | - |
dc.identifier.spage | 2817 | - |
dc.identifier.epage | 2820 | - |
dc.identifier.isi | WOS:000257211400051 | - |
dc.identifier.issnl | 1523-7052 | - |