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- Publisher Website: 10.1002/adsc.201000400
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Article: Copper-catalyzed four-component reaction of Baylis-Hillman adducts with alkynes, sulfonyl azides and alcohols
Title | Copper-catalyzed four-component reaction of Baylis-Hillman adducts with alkynes, sulfonyl azides and alcohols |
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Authors | |
Keywords | Baylis-Hillman Adducts Cascade Reactions Copper Imidates Ketenimines Multicomponent Reactions |
Issue Date | 2010 |
Publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=1615-4150 |
Citation | Advanced Synthesis And Catalysis, 2010, v. 352 n. 14-15, p. 2432-2436 How to Cite? |
Abstract | 4-(Alkoxycarbonyl)-pent-4-enimidates were regioselectively synthesized via a copper-catalyzed four-component reaction of Baylis-Hillman adducts with terminal alkynes, sulfonyl azides and alcohols. The procedure is concise, general and efficient. The resulting pentenimidates could be further transformed to 3-methylene-2,3-dihydroindene-1-imidates. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Persistent Identifier | http://hdl.handle.net/10722/168487 |
ISSN | 2023 Impact Factor: 4.4 2023 SCImago Journal Rankings: 1.020 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Song, W | en_US |
dc.contributor.author | Lei, M | en_US |
dc.contributor.author | Shen, Y | en_US |
dc.contributor.author | Cai, S | en_US |
dc.contributor.author | Lu, W | en_US |
dc.contributor.author | Lu, P | en_US |
dc.contributor.author | Wang, Y | en_US |
dc.date.accessioned | 2012-10-08T03:19:32Z | - |
dc.date.available | 2012-10-08T03:19:32Z | - |
dc.date.issued | 2010 | en_US |
dc.identifier.citation | Advanced Synthesis And Catalysis, 2010, v. 352 n. 14-15, p. 2432-2436 | en_US |
dc.identifier.issn | 1615-4150 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/168487 | - |
dc.description.abstract | 4-(Alkoxycarbonyl)-pent-4-enimidates were regioselectively synthesized via a copper-catalyzed four-component reaction of Baylis-Hillman adducts with terminal alkynes, sulfonyl azides and alcohols. The procedure is concise, general and efficient. The resulting pentenimidates could be further transformed to 3-methylene-2,3-dihydroindene-1-imidates. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | en_US |
dc.language | eng | en_US |
dc.publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=1615-4150 | en_US |
dc.relation.ispartof | Advanced Synthesis and Catalysis | en_US |
dc.subject | Baylis-Hillman Adducts | en_US |
dc.subject | Cascade Reactions | en_US |
dc.subject | Copper | en_US |
dc.subject | Imidates | en_US |
dc.subject | Ketenimines | en_US |
dc.subject | Multicomponent Reactions | en_US |
dc.title | Copper-catalyzed four-component reaction of Baylis-Hillman adducts with alkynes, sulfonyl azides and alcohols | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lu, W:luwei@hku.hk | en_US |
dc.identifier.authority | Lu, W=rp00754 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/adsc.201000400 | en_US |
dc.identifier.scopus | eid_2-s2.0-78349294853 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-78349294853&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 352 | en_US |
dc.identifier.issue | 14-15 | en_US |
dc.identifier.spage | 2432 | en_US |
dc.identifier.epage | 2436 | en_US |
dc.identifier.isi | WOS:000284003100015 | - |
dc.publisher.place | Germany | en_US |
dc.identifier.scopusauthorid | Song, W=35504060200 | en_US |
dc.identifier.scopusauthorid | Lei, M=24921890700 | en_US |
dc.identifier.scopusauthorid | Shen, Y=36024091100 | en_US |
dc.identifier.scopusauthorid | Cai, S=36624907500 | en_US |
dc.identifier.scopusauthorid | Lu, W=27868087600 | en_US |
dc.identifier.scopusauthorid | Lu, P=36072831700 | en_US |
dc.identifier.scopusauthorid | Wang, Y=35243602700 | en_US |
dc.identifier.issnl | 1615-4150 | - |