Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Olivier Thillaye du Boullay"'
Autor:
Julie Klein, Cécile Caubet, Mylène Camus, Manousos Makridakis, Colette Denis, Marion Gilet, Guylène Feuillet, Simon Rascalou, Eric Neau, Luc Garrigues, Olivier Thillaye du Boullay, Harald Mischak, Bernard Monsarrat, Odile Burlet-Schiltz, Antonia Vlahou, Jean Sébastien Saulnier-Blache, Jean-Loup Bascands, Joost P. Schanstra
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2020, 10 (1), pp.14898. ⟨10.1038/s41598-020-71950-7⟩
Scientific Reports, 2020, 10 (1), pp.14898. ⟨10.1038/s41598-020-71950-7⟩
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Scientific Reports, Nature Publishing Group, 2020, 10 (1), pp.14898. ⟨10.1038/s41598-020-71950-7⟩
Scientific Reports, 2020, 10 (1), pp.14898. ⟨10.1038/s41598-020-71950-7⟩
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
International audience; Abstract While blocking the renin angiotensin aldosterone system (RAAS) has been the main therapeutic strategy to control diabetic kidney disease (DKD) for many years, 25–30% of diabetic patients still develop the disease. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ed44fa7306659132bfb73167665602c8
https://www.hal.inserm.fr/inserm-03268523
https://www.hal.inserm.fr/inserm-03268523
Autor:
Emmanuel Nicolas, Olivier Thillaye Du Boullay, Alexia Ohleier, Elixabete Rezabal, Florian D'Accriscio, Gilles Frison, Marie Fustier-Boutignon, Nicolas Mézailles, Nathalie Saffon-Merceron, Matthieu Demange, Noel Nebra
Publikováno v:
Organometallics
Organometallics, American Chemical Society, 2020, 39 (10), pp.1688-1699. ⟨10.1021/acs.organomet.9b00834⟩
Organometallics, 2020, 39 (10), pp.1688-1699. ⟨10.1021/acs.organomet.9b00834⟩
Organometallics, American Chemical Society, 2020, 39 (10), pp.1688-1699. ⟨10.1021/acs.organomet.9b00834⟩
Organometallics, 2020, 39 (10), pp.1688-1699. ⟨10.1021/acs.organomet.9b00834⟩
International audience; The complexes (Cy2PC3H6PCy2)Ni(η2-arene) (arene = toluene (3), naphthalene (4)) have been synthesized and studied in detail. Displacement reactions of the toluene ligand afford the complexes (Cy2PC3H6PCy2)Ni(η2-styrene) (5),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6d78252d79b24d48b741faffa4adc06
https://hal.archives-ouvertes.fr/hal-02911077/file/postprint.pdf
https://hal.archives-ouvertes.fr/hal-02911077/file/postprint.pdf
Autor:
Ionut-Tudor Moraru, Sonia Mallet-Ladeira, Olivier Thillaye du Boullay, David Madec, Noémi Deak, Gabriela Nemes
Publikováno v:
Dalton Transactions
Dalton Transactions, Royal Society of Chemistry, 2019, 48 (7), pp.2399-2406. ⟨10.1039/c8dt05116j⟩
Dalton Transactions, Royal Society of Chemistry, 2019, 48 (7), pp.2399-2406. ⟨10.1039/c8dt05116j⟩
New chiral heteroleptic germanium(ii) and tin(ii) metallylenes were obtained using 1-(para-tolylsulfinyl)-3-tosyl-5-tert-butyl-benzene as a non-symmetric O,C,O-chelating pincer ligand. Crystallographic analysis and DFT calculations indicate that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec7437a1b92e914e0cfff0acb44b4852
https://hal.archives-ouvertes.fr/hal-02321975
https://hal.archives-ouvertes.fr/hal-02321975
Publikováno v:
Polymer Chemistry. 6:989-997
Amide end-capped PLA can be efficiently prepared by taking advantage of the ability of amines to ring-open lactide. A two-step one-pot strategy has been developed in which primary or secondary amines are reacted with an excess of lactide prior to the
Autor:
Jean-Pierre Diehl, Didier Bourissou, Olivier Thillaye du Boullay, Blanca Martin-Vaca, Nathalie Saffon
Publikováno v:
Biomacromolecules. 11:1921-1929
The (3S)-[(benzyloxycarbonyl)ethyl]-1,4-dioxan-2,5-dione (BED) was prepared in four steps starting from glutamic acid and bromoacetyl bromide. According to X-ray diffraction analysis, the pendant functional group is located in equatorial position and
Autor:
Rémy Fortrie, Messaoud Mazari, Gérard Buono, Frédéric Fotiadu, Yuan Zhang, Julien Leclaire, Didier Bourissou, Colin Bonduelle, Olivier Thillaye du Boullay, Innocenzo de Riggi, Blanca Martin-Vaca
Publikováno v:
Chemistry
Chemistry, 2013, 19 (34), pp.11301-9. ⟨10.1002/chem.201301275⟩
Chemistry, Wiley, 2013, 19 (34), pp.11301-9. ⟨10.1002/chem.201301275⟩
Chemistry, 2013, 19 (34), pp.11301-9. ⟨10.1002/chem.201301275⟩
Chemistry, Wiley, 2013, 19 (34), pp.11301-9. ⟨10.1002/chem.201301275⟩
International audience; A new family of 2-hydroxyalk(en/yn)ylimidazoles has been evaluated as serine–histidine bare dyad models for the ring-opening reaction of L-lacOCA, a cyclic O-carboxyanhydride. These models were selected to unravel the implic
Publikováno v:
Chemical Communications
Chemical Communications, Royal Society of Chemistry, 2008, pp.1786-1788
HAL
Chemical Communications, Royal Society of Chemistry, 2008, pp.1786-1788
HAL
Well-controlled poly(alpha-hydroxyacids) featuring pendant carboxylic acid groups were prepared under mild conditions via DMAP-catalyzed ROP of the O-carboxyanhydrides derived from glutamic and lactic acids.
Autor:
Blanca Martin-Vaca, Didier Bourissou, Aurelie Alba, Fatima Oukhatar, Olivier Thillaye du Boullay
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2008, pp.4669-4672
Organic Letters, American Chemical Society, 2008, pp.4669-4672
The preparation of the (1-naphthyl)(trifluoromethyl) O-carboxy-anhydride 1 and its use as a chiral derivatizing agent with several alpha-chiral primary amines are reported. The very large Delta delta(RS) values observed in (1)H NMR have been correlat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e141160e7ff336aa00544fa2e1db822
https://hal.archives-ouvertes.fr/hal-00371328
https://hal.archives-ouvertes.fr/hal-00371328
Autor:
† Blanca Martin-Vaca, Olivier Thillaye du Boullay, Didier Bourissou, Emmanuel Marchal, and Fernando P. Cossío
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2006, 128, pp.16442-16443
Journal of the American Chemical Society, American Chemical Society, 2006, 128, pp.16442-16443
The alpha-lactone equivalent lacOCA exhibits remarkable reactivity compared with lactide in nucleophile-catalyzed ROP. PLAs of controlled molecular weights and narrow polydispersities are typically obtained under mild conditions using DMAP and variou
Autor:
Rémy Fortrie, Christian Roussel, Mayuko Takahashi, Rémi Plamont, Innocenzo de Riggi, Julien Leclaire, Messaoud Mazari, Teodor Silviu Balaban, Olivier Thillaye du Boullay, Yoshihiro Kikkawa, Didier Bourissou, Gérard Buono, Yuan Zhang, Frédéric Fotiadu, Michel Giorgi, Blanca Martin-Vaca, Masatoshi Kanesato, Anita Chan Kam Shun, Colin Bonduelle
Publikováno v:
Chemistry - A European Journal. 19:11101-11101