Publication
Cycloaddition reactions of nitrosoalkenes, azoalkenes and nitrile oxides mediated by hydrotalcite
dc.contributor.author | Lemos, A. | |
dc.contributor.author | Lourenço, J. P. | |
dc.date.accessioned | 2012-03-13T23:23:41Z | |
dc.date.available | 2012-03-13T23:23:41Z | |
dc.date.issued | 2010 | |
dc.date.updated | 2012-03-12T17:45:40Z | |
dc.description.abstract | Mg:Al 3:1 hydrotalcite (Ht), used in catalytic quantities, promotes the generation of nitrosoalkenes, azoalkenes and nitrile oxides. These can be intercepted in situ by heterocycles and olefins in [4+2] and [3+2] cycloaddition reactions, producing dihydro-1,2-oxazines, tetrahydropyridazines and isoxazolines. The regeneration and reuse of Ht without loss of activity and the absence of organic solvent are the main advantages of this methodology. | por |
dc.identifier.citation | ARKIVOC, v, 170-182, 2010. | por |
dc.identifier.other | AUT: ALE01411; JLO01215; | |
dc.identifier.uri | http://hdl.handle.net/10400.1/939 | |
dc.language.iso | eng | por |
dc.peerreviewed | yes | por |
dc.subject | Cycloaddition | por |
dc.subject | Hydrotalcite | por |
dc.title | Cycloaddition reactions of nitrosoalkenes, azoalkenes and nitrile oxides mediated by hydrotalcite | por |
dc.type | journal article | |
dspace.entity.type | Publication | |
person.familyName | Lemos | |
person.familyName | Lourenço | |
person.givenName | Americo | |
person.givenName | João P. | |
person.identifier | 634248 | |
person.identifier.ciencia-id | A81D-6DC7-31E4 | |
person.identifier.ciencia-id | F81F-A1F0-2A7C | |
person.identifier.orcid | 0000-0001-9588-4555 | |
person.identifier.orcid | 0000-0002-0501-6672 | |
person.identifier.rid | B-4892-2008 | |
person.identifier.rid | A-7758-2008 | |
person.identifier.scopus-author-id | 11139694000 | |
person.identifier.scopus-author-id | 57195730600 | |
rcaap.rights | openAccess | por |
rcaap.type | article | por |
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