Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tamás T. Novák"'
Publikováno v:
Results in Chemistry, Vol 7, Iss , Pp 101309- (2024)
A study on some halofluorination and fluoroselenation protocols of various functionalized cyclic olefins, such as esters, lactams or amino esters as model compounds is presented. The ring olefin bond functionalizations were based on their activation
Externí odkaz:
https://doaj.org/article/b4fd2726e9904c4b8b41c6cd7597900e
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 2562-2575 (2020)
A study exploring halofluorination and fluoroselenation of some cyclic olefins, such as diesters, imides, and lactams with varied functionalization patterns and different structural architectures is described. The synthetic methodologies were based o
Externí odkaz:
https://doaj.org/article/86edf0fd1b514691b02818b6e88e124b
Autor:
Zsanett Benke, Tamás T. Novák, Attila Márió Remete, Anas Semghouli, Santos Fustero, Loránd Kiss
Publikováno v:
Chemistry – An Asian Journal. 16:3873-3881
Novel functionalized azaheterocycles with multiple chiral centers have been accessed from readily available norbornene β-amino acids or β-lactams across a stereocontrolled synthetic route, based on ring-opening metathesis (ROM) of the staring unsat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cc6a137cef72c59a3330d776a6ba965
https://doi.org/10.1002/asia.202100956
https://doi.org/10.1002/asia.202100956
Publikováno v:
Chemistry, an Asian journal. 17(15)
Due to the increasing relevance of fluorine-containing organic molecules in drug design, the synthesis of organofluorine compounds has gained high significance in synthetic organic chemistry. Trifluoromethylative difunctionalizations of carbon-carbon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22af733ef65d82ba268f70c3385a517d
https://pubmed.ncbi.nlm.nih.gov/35584374
https://pubmed.ncbi.nlm.nih.gov/35584374
The synthesis of some new functionalized azaheterocyclic β-amino esters with multiple stereocenters has been achieved from readily available unsaturated bicyclic β-amino acids by a stereocontrolled synthetic protocol involving N-allylation/propargy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56ad5f64de1d2ee8cd5d0fe12e207176
https://doi.org/10.1055/a-1877-3822
https://doi.org/10.1055/a-1877-3822
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 2562-2575 (2020)
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 2562-2575 (2020)
A study exploring halofluorination and fluoroselenation of some cyclic olefins, such as diesters, imides, and lactams with varied functionalization patterns and different structural architectures is described. The synthetic methodologies were based o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e59a249fde57107b79589e262038fe8
https://pubmed.ncbi.nlm.nih.gov/33133288
https://pubmed.ncbi.nlm.nih.gov/33133288
Autor:
Wolf T; Central European University, Vienna, Austria. thomaswolf.cogsci@gmail.com., Novák T; University of Bristol, Bristol, UK., Knoblich G; Central European University, Vienna, Austria.
Publikováno v:
Scientific reports [Sci Rep] 2023 Jun 30; Vol. 13 (1), pp. 10584. Date of Electronic Publication: 2023 Jun 30.