Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Martín J. Riveira"'
Autor:
Melina G. Di Liberto, Agustín J. Caldo, Ariel D. Quiroga, Martín J. Riveira, Marcos G. Derita
Publikováno v:
ACS Omega, Vol 5, Iss 13, Pp 7481-7487 (2020)
Externí odkaz:
https://doaj.org/article/73a15eecabf643c2842fb8aa9be4087f
Publikováno v:
ARKIVOC, Vol 2011, Iss 7, Pp 162-169 (2011)
Externí odkaz:
https://doaj.org/article/c8d1cae19ab243b788cd2be1f998fbb0
Publikováno v:
The Journal of Organic Chemistry. 87:13469-13479
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d554fbd0ed2b13e50f29cff25ceba554
https://doi.org/10.1021/acs.joc.2c01783
https://doi.org/10.1021/acs.joc.2c01783
Publikováno v:
The Journal of organic chemistry. 86(17)
Studies on Knoevenagel condensations between conjugated dienals and 4-hydroxy-2-pyridone/quinolone-type 1,3-dicarbonyl equivalents led to the development of a simple one-pot strategy to access citridone A and related synthetic cyclopenta[b]furopyrido
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98252cd7b393fcb5d3a5dd066aab19c4
https://pubmed.ncbi.nlm.nih.gov/34410723
https://pubmed.ncbi.nlm.nih.gov/34410723
Publikováno v:
The Journal of Organic Chemistry. 84:3671-3677
The photochemical behavior of several dienones was studied under aerobic conditions. 2-Allylidene-1,3-cycloalkanediones prepared via Knoevenagel-type condensation between simple readily available 1,3-dicarbonyl substrates and á,â-unsaturated aldehy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5a606260ee66410f3bbc99577c8ca91
https://doi.org/10.1021/acs.joc.8b03279
https://doi.org/10.1021/acs.joc.8b03279
Autor:
Martín J. Riveira
Publikováno v:
Journal of natural products. 83(4)
The synthesis of the biologically active alkaloid simulenoline, isolated from the roots of Zanthoxylum simulans, is reported. The natural product was assembled from simple commercial reagents via initial domino Knoevenagel/oxa-6p-electrocyclization f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d44dd6dac02615795fb96ec8aec685c
https://pubmed.ncbi.nlm.nih.gov/32233438
https://pubmed.ncbi.nlm.nih.gov/32233438
Autor:
Ernesto G. Mata, Martín J. Riveira
Publikováno v:
European Journal of Organic Chemistry. 2017:1675-1693
Fil: Riveira, Martin Jorge. Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Rosario. Instituto de Quimica Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquimicas y Farmaceuticas.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::defe93cfc36a903d6ecd2a1927973d94
https://doi.org/10.1002/ejoc.201601487
https://doi.org/10.1002/ejoc.201601487
Publikováno v:
Frontiers in Natural Products, Vol 2 (2024)
Externí odkaz:
https://doaj.org/article/d2c328accdc74d30aa76b8bec39bc94e
Publikováno v:
Organic letters. 20(22)
Molecular iodine was identified as an efficient catalyst for the cycloisomerization of conjugated dienals to substituted 2-cyclopentenones. DFT calculations suggested an unexpected concerted character for this cyclization. Fil: Marsili, Lucía A.. Un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9923067c5adb8787e910c2dc5601611
https://pubmed.ncbi.nlm.nih.gov/30403484
https://pubmed.ncbi.nlm.nih.gov/30403484
A stereoselective multicomponent reaction involving Meldrum's acid, a conjugated dienal, and an alcohol is reported. Valuable cyclopenta[b]furan-2-ones are obtained as products of this straightforward transformation, which is accompanied by the forma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd949782885b76ed6ac29d023bbc4f21
http://pubs.acs.org/doi/10.1021/acs.orglett.8b01567
http://pubs.acs.org/doi/10.1021/acs.orglett.8b01567
