Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Guillaume Maitro"'
Autor:
Julia Baron, Stefan Heinig, Mathias Krusch, Eric Hoffmann, Steffen Killian, David B Karpf, Kennett Sprogøe, Joachim Zettler, Caroline E Rasmussen, Felix Cleemann, Guillaume Maitro, Vibeke Miller Breinholt, Susanne Pihl, Frank Faltinger, Lars Holten-Andersen, Thomas Wegge
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 34(11)
Hypoparathyroidism (HP) is a condition of parathyroid hormone (PTH) deficiency leading to abnormal calcium and phosphate metabolism. The mainstay of therapy consists of vitamin D and calcium supplements, as well as adjunct Natpara (PTH(1-84)). Howeve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e2982cd54c14c0c3fd70191b05fee2a
https://pubmed.ncbi.nlm.nih.gov/31291476
https://pubmed.ncbi.nlm.nih.gov/31291476
Publikováno v:
Tetrahedron: Asymmetry. 21:1075-1084
An escapade in the world of sulfenate anions is described and shows that these nucleophiles, despite being described as unstable species, are mild and efficient sulfinylating agents, allowing access to a variety of allyl and aryl sulfoxides under smo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37f96b710803d8795da9d1d219426e4f
https://doi.org/10.1016/j.tetasy.2010.05.035
https://doi.org/10.1016/j.tetasy.2010.05.035
Autor:
David Madec, Guillaume Maitro, Guillaume Prestat, Giuseppe Paladino, Giovanni Poli,‡ and, Anny Jutand
Publikováno v:
Organometallics
Organometallics, American Chemical Society, 2007, 26 (2), pp.455. ⟨10.1021/om060846x⟩
Organometallics, 2007, 26 (2), pp.455. ⟨10.1021/om060846x⟩
Organometallics, American Chemical Society, 2007, 26 (2), pp.455. ⟨10.1021/om060846x⟩
Organometallics, 2007, 26 (2), pp.455. ⟨10.1021/om060846x⟩
The kinetics of the oxidative addition of bidentate ligand-chelated Pd0 complexes to phenyl iodide and bromide has been studied via cyclic voltammetry. The dibenzylideneacetone (dba) delivered by t...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::957d1092a973046e3b8be81e8929fa94
https://doi.org/10.1021/om060846x
https://doi.org/10.1021/om060846x
Autor:
Giuliano Giambastiani, Francesco Mingoia, Cristian Macovei, David Madec, Guillaume Maitro, Giovanni Poli
Publikováno v:
European journal of organic chemistry
5 (2005): 552–557. doi:10.1002/ejoc.200400547
info:cnr-pdr/source/autori:D. Madec (1); F. Mingoia (2); C. Macovei (1), G. Maitro (1); G. Giambastiani (3); G. Poli (1)/titolo:New Enantiopure Bis-Thioether and Bis-Sulfoxide Ligands from Benzothiophene/doi:10.1002%2Fejoc.200400547/rivista:European journal of organic chemistry (Print)/anno:2005/pagina_da:552/pagina_a:557/intervallo_pagine:552–557/volume:5
5 (2005): 552–557. doi:10.1002/ejoc.200400547
info:cnr-pdr/source/autori:D. Madec (1); F. Mingoia (2); C. Macovei (1), G. Maitro (1); G. Giambastiani (3); G. Poli (1)/titolo:New Enantiopure Bis-Thioether and Bis-Sulfoxide Ligands from Benzothiophene/doi:10.1002%2Fejoc.200400547/rivista:European journal of organic chemistry (Print)/anno:2005/pagina_da:552/pagina_a:557/intervallo_pagine:552–557/volume:5
The C2-symmetric compound 2,3,2,3-tetrahydro-2,2-bi(benzo[b]thiophenyl) and three diastereomeric bis(oxide) derivatives can be synthesized in a few steps from benzo[b]-thiophene by oxidative homocoupling of (R)-2,3-dihydro-benzo[b]thiophene 1-oxide.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb949edaf616ed529a327c710afe08c1
https://doi.org/10.1002/ejoc.200400547
https://doi.org/10.1002/ejoc.200400547
Autor:
Guillaume Maitro, Giovanni Poli, David Madec, Sophie Vogel, Guillaume Prestat, Xavier Bantreil
Publikováno v:
Tetrahedron Letters. 51:1459-1461
Asymmetric intramolecular palladium-catalyzed allylic alkylation allowing access to disubstituted sulfinyl γ-lactams is described. The use of unsaturated amides bearing a sulfinyl group of defined absolute configuration together with enantiopure BIN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3efd7d05f4af9e29a4c75dde3fde91b6
https://doi.org/10.1016/j.tetlet.2010.01.012
https://doi.org/10.1016/j.tetlet.2010.01.012
Publikováno v:
ChemInform. 41
An escapade in the world of sulfenate anions is described and shows that these nucleophiles, despite being described as unstable species, are mild and efficient sulfinylating agents, allowing access to a variety of allyl and aryl sulfoxides under smo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20a9d1b76b1992cdefdb2888f1915926
https://doi.org/10.1002/chin.201048247
https://doi.org/10.1002/chin.201048247
Autor:
Giovanni Poli, Guillaume Maitro, Sophie Vogel, Mounel Sadaoui, Guillaume Prestat, David Madec
Publikováno v:
ChemInform. 39
Arylation of various sulfenate anions generated from β-sulfinyl esters by retro-Michael reaction in the presence of palladium(0) and enantiopure ligands gave the corresponding aryl sulfoxides in enantio-enriched form. The Josiphos-type ligand (R)-(S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f3ba7a71aaf957a34303843e1976fe3
https://doi.org/10.1002/chin.200822090
https://doi.org/10.1002/chin.200822090
Autor:
David Madec, Guillaume Prestat, Guillaume Maitro, Sophie Vogel, Giovanni Poli, Mounel Sadaoui
Publikováno v:
Organic letters. 9(26)
Arylation of various sulfenate anions generated from beta-sulfinyl esters by retro-Michael reaction in the presence of palladium(0) and enantiopure ligands gave the corresponding aryl sulfoxides in enantio-enriched form. The Josiphos-type ligand (R)-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1ff97ed24c7e7996e1e5ec72b5d20f6
https://pubmed.ncbi.nlm.nih.gov/18034497
https://pubmed.ncbi.nlm.nih.gov/18034497
Publikováno v:
ChemInform. 38
[Structure: see text] Palladium-catalyzed arylation of sulfenate anions generated from beta-sulfinyl esters can take place under biphasic conditions. This hitherto unknown reaction provides a simple, mild, and efficient route to aryl sulfoxides in go
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b515f253b4ac3f4b4487bb25be9fd4dd
https://doi.org/10.1002/chin.200717083
https://doi.org/10.1002/chin.200717083
Publikováno v:
The Journal of organic chemistry. 71(19)
Palladium-catalyzed allylic alkylation of sulfenate anions, generated from beta-sulfinylesters by retro-Michael reaction, can take place under biphasic conditions. This new reaction provides a simple, mild, and efficient route to allyl sulfoxides in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7b168ee06e0a1954129c9a1551cf1c3
https://pubmed.ncbi.nlm.nih.gov/16958541
https://pubmed.ncbi.nlm.nih.gov/16958541