Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Irem Yalavac"'
Publikováno v:
Tetrahedron. 71:4124-4131
The cis-fused lactones were the major products isolated from Diels–Alder reactions of (2E,4E)-2,4-dimethylhexa-2,4-dienyl methyl fumarate and maleate and from the cyclisation of the all (E)-2,4,6,8-tetramethyldeca-2,4,6,8-tetraenyl methyl fumarate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b88fa608cd65a27b004f031393a6aef
https://doi.org/10.1016/j.tet.2015.04.101
https://doi.org/10.1016/j.tet.2015.04.101
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f04cc806e9e5f955939b438b95ddaa3c
https://doi.org/10.1002/chin.201647260
https://doi.org/10.1002/chin.201647260
Publikováno v:
ChemInform. 46
Both inter- and intramolecular Diels—Alder reactions of dienyl methyl fumarate [e.g. (I) and (III)] give cis-fused lactones with a methyl bearing quaternary centre as the major products because of the influence of the methyl substituent.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e303dbd73e02f2ce550a2b18ecb660ae
https://doi.org/10.1002/chin.201539097
https://doi.org/10.1002/chin.201539097
Publikováno v:
ChemInform. 46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b895e6863d1c00818530094c068fbd77
https://doi.org/10.1002/chin.201511113
https://doi.org/10.1002/chin.201511113
Samarium (ii) iodide (SmI2, Kagan's reagent) is one of the most important reducing agents in organic synthesis. Its unique reactivity and selectivity makes it ideal for mediating key steps in target syntheses often providing outcomes that simply cann
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd977133797e3f903c2b9da98489861c
https://doi.org/10.1039/9781782623960-00001
https://doi.org/10.1039/9781782623960-00001
Publikováno v:
Chemical communications (Cambridge, England). 50(85)
The SmI2–H2O reagent system mediates challenging 5-exo/6-exo lactone radical cascade cyclisations that deliver carbo[5.4.0]bicyclic motifs in a diastereoselective, one-pot process that establish two new carbocyclic rings and four stereocentres.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d3e4b139e3308bac37c6bd16e068e30
https://pubmed.ncbi.nlm.nih.gov/25211167
https://pubmed.ncbi.nlm.nih.gov/25211167