Zobrazeno 1 - 10
of 180
pro vyhledávání: '"Christian Jarry"'
Autor:
Puria Parvini, Daniel Buser, Benjamin Evans Pippenger, Jean‐Claude Imber, Andreas Stavropoulos, Benjamin Bellón, Christian Jarry, Frank Schwarz
Publikováno v:
Journal of clinical periodontologyREFERENCES.
To histologically evaluate the influence of (1) loading and (2) grafting on osseointegration and peri-implant soft-tissue healing at immediately placed, self-cutting progressive tissue-level implants (TLX) in a minipig model.TLX implants (n = 56) wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4cf716441270694bce795023f7da46b
https://pubmed.ncbi.nlm.nih.gov/36217692
https://pubmed.ncbi.nlm.nih.gov/36217692
Autor:
Banu Karayazgan, Stefan Roehling, Christian Jarry, Daniel Buser, Vedrana Braut, Lauren Bohner, Bjarni E. Pjetursson, Michael Gahlert, Robert A. Jaffin, Stephen T. Chen, Charlotte Stilwell, Lira Rahman, Steven E Eckert, Hugo Albera, Andreas Schlegel, Adam Hamilton, Waldemar D. Polido, Juhani Laine, German O. Gallucci, Wei-Shao Lin, William Martin, Tara Aghaloo, Irena Sailer, Anja Zembic, Christiaan Vorster, Makato Shiota, Dean Morton, Wenjie Zhou, Anthony Dawson
Publikováno v:
Clinical Oral Implants Research, Vol. 29, No S16 (2018) pp. 215-223
Publisher's version (útgefin grein)
Objectives: Working Group 2 was convened to address topics relevant to prostho-dontics and dental implants. Systematic reviews were developed according to fo -cused questions addressing (a) the number of impl
Objectives: Working Group 2 was convened to address topics relevant to prostho-dontics and dental implants. Systematic reviews were developed according to fo -cused questions addressing (a) the number of impl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c024c142fca90757c14e4533b4094ff
https://hdl.handle.net/20.500.11815/1412
https://hdl.handle.net/20.500.11815/1412
Autor:
Jean‐Michel Leger, Christian Jarry, Sylvain Routier, Stéphane Massip, Frédéric Buron, Chloé Copin
Publikováno v:
European Journal of Organic Chemistry. 2015:6932-6942
An original and efficient palladium-catalyzed amination of imidazo[2,1-b][1,3,4]thiadiazole is reported. The SNAr and Buchwald–Hartwig cross-coupling reactions were investigated to access C-2 aminated imidazo[1,2-b][1,3,4]thiadiazole derivatives. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f92d4bda5ab536bb9cc3640af1a7cbbc
https://doi.org/10.1002/ejoc.201500977
https://doi.org/10.1002/ejoc.201500977
Autor:
Sylvain Routier, Christian Jarry, Rabia Belaroussi, Nathalie Percina, Mathieu Marchivie, Gérald Guillaumet, Ahmed El Hakmaoui, Stéphane Massip, Agnes Chartier, Mohamed Akssira
Publikováno v:
European Journal of Organic Chemistry. 2015:4006-4017
The first efficient synthesis of various 1,4-disubstituted pyrido[1′,2′:1,5]pyrazolo[3,4-d]pyridazines is reported. The reactivity toward chlorine release at the C-1 and C-4 positions was investigated. SNAr and palladium-catalysed cross-coupling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3d4ddcc6331934116c7857aa0c74550
https://doi.org/10.1002/ejoc.201500294
https://doi.org/10.1002/ejoc.201500294
Autor:
Christian Jarry, Stéphane Massip, Yves Troin, Isabelle Abrunhosa-Thomas, Gérald Guillaumet, Abderrahman El Bouakher
Publikováno v:
European Journal of Organic Chemistry. 2015:556-569
An efficient, simple, and convenient synthetic procedure for the synthesis of tetracyclic spirooxindole derivatives, starting from N-protected isatins and 2-fluoropyridine, was successfully developed. It enables the facile formation of a new class of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::693744e9f00e1ab3715c6e2710e2797c
https://doi.org/10.1002/ejoc.201403292
https://doi.org/10.1002/ejoc.201403292
Autor:
Christelle Pillard, Gérald Guillaumet, Philippe Bernard, Robert Kiss, Mathieu Marchivie, Stéphane Massip, Christian Jarry, Sandrine Grosse, Véronique Mathieu
Publikováno v:
European Journal of Medicinal Chemistry. 84:718-730
Synthesis and functionalization strategies of the imidazo[1,2-b]pyrazole core were developed giving a rapid access to three series of novel imidazo[1,2-b]pyrazole type derivatives: C-2/C-6/C-7 trisubstituted, C-2/C-3/C-6 tri(hetero)arylated and C-2/C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76ac5db9b860d065b798371dc7cc9355
https://doi.org/10.1016/j.ejmech.2014.07.057
https://doi.org/10.1016/j.ejmech.2014.07.057
Autor:
Mikael Le Meur, Stéphane Bourg, Sylvain Routier, Mathieu Marchivie, Gérald Guillaumet, Christian Jarry, Stéphane Massip
Publikováno v:
European Journal of Organic Chemistry. 2014:3704-3714
An efficient and convenient method was developed for the formation of polysubstituted thiazolo[3,2-b][1,2,4]triazoles through C-5 (het)arylation. The direct C–H activation protocol giving access to di- and trisubstituted derivatives in excellent yi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb34b9d47440ce17a0363cfafb252369
https://doi.org/10.1002/ejoc.201402193
https://doi.org/10.1002/ejoc.201402193
Autor:
Johnny Vercouillie, Gérald Guillaumet, Mathieu Marchivie, Sylvie Chalon, Sylvain Routier, Franck Suzenet, Christian Jarry, Raja Ben Othman, Stéphane Massip
Publikováno v:
European Journal of Organic Chemistry. 2014:3225-3231
An efficient and convenient method was developed for the formation of S-substituted thiotriazoles through an unprecedented organometallic addition and subsequent ring-opening sequence of 3-substituted [1,2,4]triazolo[3,4-b][1,3,4]thiadiazole. The met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2f117beba02a49ae1c2190cf9c90071
https://doi.org/10.1002/ejoc.201400151
https://doi.org/10.1002/ejoc.201400151
Autor:
Jean A. Boutin, Arnaud Gohier, Christian Jarry, Olivier Nosjean, Pascal Berthelot, Daniel-Henri Caignard, Mohamed Ettaoussi, Clotilde Mannoury la Cour, Basile Pérès, Philippe Delagrange, Saïd Yous
Publikováno v:
Med. Chem. Commun.. 5:1303-1308
We report herein the racemic resolution and pharmacological evaluation of naphthalenic ligand analogues of compound 3a. Propionamide 3b and fluoroacetamide 3c showed a good pharmacological profile towards MT1, MT2 and 5-HT2C. Hence, their enantiomers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ac8e31d57e74d2935acce5f3f510662
https://doi.org/10.1039/c4md00149d
https://doi.org/10.1039/c4md00149d
Publikováno v:
Clinical Oral Implants Research. 30:242-242
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::101ce1a4ab7598e751fc3331ef116204
https://doi.org/10.1111/clr.198_13509
https://doi.org/10.1111/clr.198_13509