Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tamara Meiresonne"'
Autor:
Tatiana Piller, Louis Maes, Pieter Claes, Elena Semina, Davie Cappoen, Paul Cos, Peter Delputte, Freya Cools, Olivier Neyrolles, Francis Holvoet, An Matheeussen, Kevin Van Calster, Norbert De Kimpe, Sven Mangelinckx, Tamara Meiresonne, Guy Caljon, Maíra Bidart de Macedo, Eveline Torfs
Publikováno v:
European journal of medicinal chemistry
Tuberculosis (TB) still has a major impact on public health. In order to efficiently eradicate this life-threatening disease, the exploration of novel anti-TB drugs is of paramount importance. As part of our program to design new 2-azaanthraquinones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::603f9641960e67fa478fd2d99ec314c1
https://pubmed.ncbi.nlm.nih.gov/31376569
https://pubmed.ncbi.nlm.nih.gov/31376569
Publikováno v:
Tetrahedron. 68:9566-9571
The stereoselective synthesis of (1R,2R)- and (1S,2S)-trans-2-(diphenylmethylideneamino)cyclopropanecarboxylic acid has been accomplished in six steps starting from (2S)- and (2R)-β-benzyl N-(tert-butoxycarbonyl)aspartate, respectively. The key-step
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6fb028221e0b8f86402adb5f6b34caf
https://doi.org/10.1016/j.tet.2012.09.078
https://doi.org/10.1016/j.tet.2012.09.078
Publikováno v:
The Journal of organic chemistry. 80(10)
N-Benzoyl β,β-difluoroenamides and N-benzoyl fluoroynamides are novel structural units which have been explored as precursors in heterocyclic synthesis. The presence of two fluorine atoms at the β-position of the enamide moiety endows unique elect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6e6638573b87232f82a2e483dd84e80
https://pubmed.ncbi.nlm.nih.gov/25901523
https://pubmed.ncbi.nlm.nih.gov/25901523
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb827721005c2b8de411985afbf2c907
https://doi.org/10.1002/chin.201441283
https://doi.org/10.1002/chin.201441283
Publikováno v:
Chemical reviews. 114(16)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7de31c33a9116ab8c1e6e34ed85a864a
https://pubmed.ncbi.nlm.nih.gov/24773209
https://pubmed.ncbi.nlm.nih.gov/24773209
Publikováno v:
ChemInform. 43
Halopropylidenemalonates like (I) are used as substrates for the synthesis of title derivatives (IV) via an aza-Michael-induced ring closure reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c14f0105c82b4245f49d05fd4151f26
https://doi.org/10.1002/chin.201212048
https://doi.org/10.1002/chin.201212048
Publikováno v:
ORGANIC & BIOMOLECULAR CHEMISTRY
Novel beta-aminocyclobutanecarboxylic acid derivatives were prepared via a sequential solvent-free aza-Michael addition of benzophenone imine across 3-halopropylidenemalonates and base-induced ring closure. These highly substituted cyclobutanedicarbo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9622da4420d02029d4196fd848d95fc4
https://hdl.handle.net/1854/LU-1997584
https://hdl.handle.net/1854/LU-1997584
