Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Thierry Boxus"'
Publikováno v:
Journal of Polymer Science Part A: Polymer Chemistry. 38:3510-3520
Organic chemistry performed at the solid-liquid interface allowed us to achieve the selective chain-end functionalization of poly(ethylene terephthalate) (PET) membranes and films with perfluorinated labels. The carboxyl endings were activated with w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40ffa33e76682a0ba7de1d8a181fb4e8
https://doi.org/10.1002/1099-0518(20001001)38:19<3510::aid-pola70>3.0.co
https://doi.org/10.1002/1099-0518(20001001)38:19<3510::aid-pola70>3.0.co
Autor:
Olivier Noiset, Jacqueline Marchand-Brynaert, Yves-Jacques Schneider, Thierry Boxus, Eric Detrait, Claude Remacle
Publikováno v:
Biomaterials. 20:1773-1782
Our aim was to replace the proteins and peptides, generally used for the biocompatibilization of polymer substrata, with synthetic molecules mimicking the RGD (Arg-Gly-Asp) active sequence. Based on the (L)-tyrosine template, RGD peptidomimetics were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4792170153ef16ee83d6809a27830ab
https://doi.org/10.1016/s0142-9612(99)00072-1
https://doi.org/10.1016/s0142-9612(99)00072-1
Autor:
Catherine Henneuse-Boxus, Thierry Boxus, Eric Dulière, null Catherine Pringalle, Lorenzo Tesolin, Yasmine Adriaensen, Jacqueline Marchand-Brynaert
Publikováno v:
Polymer. 39:5359-5369
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3196f58ea0746ebe4cd37a24c5ca27fd
https://doi.org/10.1016/s0032-3861(97)10216-6
https://doi.org/10.1016/s0032-3861(97)10216-6
Autor:
Catherine Henneuse-Boxus, Catherine Pringalle, Lorenzo Tesolin, Yasmine Adriaensen, Eric Dulière, Thierry Boxus, Jacqueline Marchand-Brynaert
Publikováno v:
Polymer. 38:1387-1394
Using 4,4'-dimethoxybenzhydrol as soluble mimic of the reduced poly(aryl ether ether ketone) (PEEK) monomer unit, we established the best experimental conditions to replace the hydroxyl group with an amine function, on the one hand, and to fix an ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b444b46f6074b96b40743bb1a0bbea7
https://doi.org/10.1016/s0032-3861(96)00661-1
https://doi.org/10.1016/s0032-3861(96)00661-1
Autor:
Yves-Jacques Schneider, Thierry Boxus, Michèle Deldime-Rubbens, Jacqueline Marchand-Brynaert, Patrick Mougenot
Publikováno v:
Polymers for Advanced Technologies. 7:589-598
Poly(ethylene terephthalate) BET) films and track-etched microporous membranes naturally display, on their surfaces, reactive chain-ends, i.e. carboxyl and hydroxyl functions. These were assayed by suitable activation (reaction with carbodiimide and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ab44299802d2b0db759543ed37610b1
https://doi.org/10.1002/(sici)1099-1581(199607)7:7<589::aid-pat551>3.0.co
https://doi.org/10.1002/(sici)1099-1581(199607)7:7<589::aid-pat551>3.0.co
Autor:
Guiseppe Pantano, Lorenzo Tesolin, Jacqueline Marchand-Brynaert, Catherine Henneuse, Thierry Boxus
Publikováno v:
Synthesis. 1996:495-501
A series of amides, lactams, carbamates, ureas and anilines, equipped with various functionalities, were readily N-alkylated with the 4,4'-dimethoxybenzhydryl residue by reaction with 4,4'-dimethoxybenzhydrol [bis(4-methoxyphenyl)methanol] in acetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7701d03290f9b5f184fd024f3cdcce5d
https://doi.org/10.1055/s-1996-4230
https://doi.org/10.1055/s-1996-4230
Publikováno v:
European journal of medicinal chemistry. 42(1)
Novel piperazinyl-amide derivatives of N-alpha-(aryl-sulfonyl)-L-arginine were synthesized as graftable thrombin inhibitors, in the context of biomaterials' design. The possible disturbance of biological activity due to a variable spacer-arm fixed on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fabd9364ff0103a75e9139c09a9a7873
https://pubmed.ncbi.nlm.nih.gov/17010480
https://pubmed.ncbi.nlm.nih.gov/17010480
Publikováno v:
Bioorganicmedicinal chemistry. 6(9)
Several RGD peptidomimetics have been prepared, in a convergent way, from the common ortho-aminotyrosine template (O-substituted with an anchorage-arm or a methyl group, and alpha N-substituted with a fluorine tag for XPS analysis), and various omega
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5ae14c12ac6f9f31aa7799a6e84c555
https://pubmed.ncbi.nlm.nih.gov/9801829
https://pubmed.ncbi.nlm.nih.gov/9801829
Publikováno v:
Tetrahedron Letters. 43:1187-1188
Methyl ethers (6a and 6b) of N-trifluoroacetyl- and N-(m-trifluoromethyl) phenylsulfonyl-6-nitro-tyrosine t-butyl ester were readily prepared by modified Mitsunobu reaction (DPPE. DIAD, MeOH). Williamson (Mel, K2CO3 or LiCO3 or NaOH under phase trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24e0ed1f71efc52f44b35f63c0006ef5
https://doi.org/10.1016/s0040-4039(01)02349-8
https://doi.org/10.1016/s0040-4039(01)02349-8