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http://hdl.handle.net/2445/96646
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DC Field | Value | Language |
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dc.contributor.author | Prieur, Vanessa | - |
dc.contributor.author | Pujol Dilmé, M. Dolors | - |
dc.contributor.author | Guillaumet, Gérald | - |
dc.date.accessioned | 2016-03-21T16:17:38Z | - |
dc.date.available | 2016-09-30T22:01:12Z | - |
dc.date.issued | 2015-09 | - |
dc.identifier.issn | 1434-193X | - |
dc.identifier.uri | http://hdl.handle.net/2445/96646 | - |
dc.description.abstract | New pyrrolo[2,3-d]pyrimidines that have aryl groups at the 2-, 4-, and 6-positions were prepared by the arylation reaction of 4-chloro-7-methyl-2-(methylthio)-6-phenylpyrrolo[2,3-d]pyrimidine (6) and the corresponding arylboronic acid under Suzuki-Miyaura conditions followed by a second arylation under Liebeskind-Srogl cross-coupling conditions. A parallel study that began with the C-2 chemoselective arylation of 6 under Liebeskind-Srogl conditions followed by a Suzuki-Miyaura coupling at C-4 was carried out, and the results of each route were compared. All of the tranformations were performed under microwave irradiation. | - |
dc.format.extent | 10 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Wiley-VCH | - |
dc.relation.isformatof | Versió postprint del document publicat a: http://dx.doi.org/10.1002/ejoc.201500625 | - |
dc.relation.ispartof | European Journal of Organic Chemistry, 2015, num. 29, p. 6547-6556 | - |
dc.relation.uri | http://dx.doi.org/10.1002/ejoc.201500625 | - |
dc.rights | (c) Wiley-VCH, 2015 | - |
dc.source | Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica) | - |
dc.subject.classification | Compostos heterocíclics | - |
dc.subject.classification | Nitrogen | - |
dc.subject.classification | Química orgànica | - |
dc.subject.classification | Reaccions químiques | - |
dc.subject.other | Heterocyclic compounds | - |
dc.subject.other | Nitrogen | - |
dc.subject.other | Organic chemistry | - |
dc.subject.other | Chemical reactions | - |
dc.title | A strategy for the triarylation of pyrrolopyrimidines by using microwave-promoted cross-coupling reactions | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/acceptedVersion | - |
dc.identifier.idgrec | 655965 | - |
dc.date.updated | 2016-03-21T16:17:43Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
Appears in Collections: | Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica) |
Files in This Item:
File | Description | Size | Format | |
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655965.pdf | 986.62 kB | Adobe PDF | View/Open |
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