Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jeny Karabline-Kuks"'
Publikováno v:
ChemistrySelect. 2:3093-3098
Capitalizing on our experience in constructing branched and dendritic monomers with functionalizable aromatic moiety at the focal point and various terminal groups, we prepared lipophilic and water-soluble dendrimers with BODIPY fluorophore in the co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f035b334375248157e3a8375c1c54d01
https://doi.org/10.1002/slct.201700377
https://doi.org/10.1002/slct.201700377
Publikováno v:
Advanced Synthesis & Catalysis. 358:3541-3554
While comparing analogous polystyrene-supported and homogeneous catalysts for the Baylis–Hillman reaction, we hypothesized that the hydrophobic envelopment of the imidazole catalytic sites of the former is responsible for the significantly better c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::330b694b42bd9ca37d04e0cef670229c
https://doi.org/10.1002/adsc.201600421
https://doi.org/10.1002/adsc.201600421
Autor:
Scott J. Miller, Jeny Karabline-Kuks, Kerem Goren, Einav Barak-Kulbak, Moshe Portnoy, Yael Shiloni
Publikováno v:
Chemistry - A European Journal. 21:1191-1197
The polystyrene-supported N-alkylimidazole-based dendritic catalysts for the Baylis-Hillman reaction exhibit one of the strongest beneficial effects of multivalent architecture ever reported for an organocatalyst. The yields in the model reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0102280f301201d5e961821d8e35c8e0
https://doi.org/10.1002/chem.201404560
https://doi.org/10.1002/chem.201404560