Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Franciane Chevot"'
Autor:
Franciane Chevot, Claire Fergus, Mathias O. Senge, John M. Southern, Stephen J. Connon, Mashael A. Alqasem, Vincent P. Kelly, Emiliano Sorrentino, Ciara McDonnell, Michelle Cotter, Karsten Hokamp
Publikováno v:
Nucleic Acids Research
Base-modification can occur throughout a transfer RNA molecule; however, elaboration is particularly prevalent at position 34 of the anticodon loop (the wobble position), where it functions to influence protein translation. Previously, we demonstrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17835b015b59f2a046cdfd5f31bb5607
https://doi.org/10.1093/nar/gkab289
https://doi.org/10.1093/nar/gkab289
Autor:
Colm Cunningham, Vincent P. Kelly, Sreeja Varghese, Claire Fergus, Franciane Chevot, Michelle Cotter, Kingston H. G. Mills, John M. Southern, Stephen J. Connon
Publikováno v:
Nucleic Acids Research
Queuine is a modified pyrrolopyrimidine nucleobase derived exclusively from bacteria. It post-transcriptionally replaces guanine 34 in transfer RNA isoacceptors for Asp, Asn, His and Tyr, in almost all eukaryotic organisms, through the activity of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f613a843e479d5653ee0a5236ff883c0
http://europepmc.org/articles/PMC5389723
http://europepmc.org/articles/PMC5389723
Publikováno v:
European Journal of Organic Chemistry. 2012:2889-2893
The synthesis of 8-amido- and 8-aminopurines by a single palladium-catalyzed protocol is reported. The method proceeds efficiently and tolerates a wide range of amides and amines as coupling partners, including aryl, alkyl, sulfone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbb62548de12a56200ed7e08054aa1e6
https://doi.org/10.1002/ejoc.201200168
https://doi.org/10.1002/ejoc.201200168
Autor:
François Radvanyi, Isabelle Bernard-Pierrot, Rosa M. Suárez, Andrea Cavagnino, Véronique Stoven, Nicolas Saettel, Franciane Chevot, Sandrine Piguel, Michel Legraverend
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2013, 61, pp.2-25. ⟨10.1016/j.ejmech.2012.06.005⟩
European Journal of Medicinal Chemistry, Elsevier, 2013, 61, pp.2-25. ⟨10.1016/j.ejmech.2012.06.005⟩
The TAM subfamily of Receptor Tyrosine Kinases (RTKs) contains three human proteins of therapeutical interest, Axl, Mer, and Tyro3. Our goal was to design a type II inhibitor specific for this family, i.e. able to interact with the allosteric pocket
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c098a66f66850a48b13d79c5cf0ed1a2
https://hal.archives-ouvertes.fr/hal-03116928
https://hal.archives-ouvertes.fr/hal-03116928
Publikováno v:
ChemInform. 43
The synthesis of 8-amido- and 8-aminopurines by a single palladium-catalyzed protocol is reported. The method proceeds efficiently and tolerates a wide range of amides and amines as coupling partners, including aryl, alkyl, sulfone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ef5425daee6879ee9295e616f846d3c
https://doi.org/10.1002/chin.201240188
https://doi.org/10.1002/chin.201240188
Publikováno v:
ChemInform. 43
An efficient microwave-assisted palladium/copper comediated C-8 direct alkenylation of purines with styryl bromides has been developed. The method is regioselective, functional group tolerant, rapid, and compatible with other related azoles. Combined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88e5138e4adccd4783ea7c9308aa34dc
https://doi.org/10.1002/chin.201212172
https://doi.org/10.1002/chin.201212172
Publikováno v:
ChemInform. 42
The titled purine diiodo purine derivative (II) is an interesting novel substrate for the preparation of 2-alkynylated and 2,8-dialkynylated purines via regioselective cross-coupling reactions with alkynes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30a7762be40ddfe93f4fc54ae576ae8d
https://doi.org/10.1002/chin.201115169
https://doi.org/10.1002/chin.201115169
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2011, pp.9542-9547
Journal of Organic Chemistry, American Chemical Society, 2011, pp.9542-9547
An efficient microwave-assisted palladium/copper comediated C-8 direct alkenylation of purines with styryl bromides has been developed. The method is regioselective, functional group tolerant, rapid, and compatible with other related azoles. Combined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d59e7aab0ea2b666fb39f3a793b78baa
https://hal.archives-ouvertes.fr/hal-00703879
https://hal.archives-ouvertes.fr/hal-00703879
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2011, 52, pp.305-307
Tetrahedron Letters, Elsevier, 2011, 52, pp.305-307
Lithiation of 6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine with LiTMP, gave access to 6-chloro-2,8-dihalogenated purine derivatives. In particular, the 6-chloro-2,8-diiodopurine derivative is an interesting new intermediate which gave regioselecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79198732ad15009f58f9cec472db4e70
https://hal.science/hal-00555071
https://hal.science/hal-00555071