Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sandra Gabillet"'
Autor:
Sabrina Bernard, Alain Wagner, Davide Audisio, Oleksandr Koniev, Sarah Bregant, Lucie Plougastel, Jijy Elyian, Elodie Decuypere, Sandra Gabillet, Sergii Kolodych, Frédéric Taran, Antoine Sallustrau, Margaux Riomet, Minh Nguyet Trinh, Ramar Arun Kumar
Publikováno v:
Angewandte Chemie International Edition. 56:15612-15616
We report the discovery of a new bioorthogonal click-and-release reaction involving iminosydnones and strained alkynes. This transformation leads to two products resulting from the ligation and fragmentation of iminosydnones under physiological condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::101bfe47ded49f18254c715e0b3185e4
https://doi.org/10.1002/anie.201708790
https://doi.org/10.1002/anie.201708790
Publikováno v:
The Journal of Organic Chemistry. 79:9894-9898
A simple and efficient method for constructing 4-arylidene-5-imidazolones was developed using a phosphine-catalyzed tandem umpolung addition and intramolecular cyclization of amidine pronucleophiles on arylpropiolates. The reaction offers a robust ro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20a0208f7da4805be657ae178e54da40
https://doi.org/10.1021/jo501922j
https://doi.org/10.1021/jo501922j
Autor:
Sandra Gabillet, Valentina Bevilacqua, Marie-Claire Nevers, Julia Quinton, Pierre Thuéry, Hervé Volland, Sergii Kolodych, Frédéric Taran, Manon Chaumonet, Christophe Créminon
Publikováno v:
Angewandte Chemie International Edition. 51:6144-6148
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11747b5bdbb3891cd2633ea43169cdbe
https://doi.org/10.1002/anie.201201451
https://doi.org/10.1002/anie.201201451
Publikováno v:
Tetrahedron Letters. 49:2083-2087
A straightforward procedure ensuring the anchoring of bisphosphonate moiety onto aromatic amines is described. The procedure yields aminoaryl 1,1-bisphosphonates known to display multiple biological activities. The described methodology has also been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c4d1f4ae08360a118b1b96564350ccb
https://doi.org/10.1016/j.tetlet.2008.01.127
https://doi.org/10.1016/j.tetlet.2008.01.127
Autor:
Frédéric Taran, Jean-Marie Gomis, Sophie Dezard, Olivier Loreau, Sandra Gabillet, Delphine Lecerclé
Publikováno v:
Synthesis. 2007:515-522
A practical one step procedure for the synthesis of 1,4-dioxane-2-one and 1,4-benzodioxine-2-one derivatives is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd2163ea31e4fb9d37e80fab10c26c82
https://doi.org/10.1055/s-2007-965900
https://doi.org/10.1055/s-2007-965900
Publikováno v:
ChemInform. 46
A simple and efficient method for constructing 4-arylidene-5-imidazolones was developed using a phosphine-catalyzed tandem umpolung addition and intramolecular cyclization of amidine pronucleophiles on arylpropiolates. The reaction offers a robust ro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::385b01bd8974bac0cbabee0b4e25bf77
https://doi.org/10.1002/chin.201514163
https://doi.org/10.1002/chin.201514163
Autor:
Elodie Decuypere, Simon Specklin, Lucie Plougastel, Hui Liu, Frédéric Taran, Sergii Kolodych, Davide Audisio, Sandra Gabillet
Publikováno v:
Organic letters. 17(2)
Copper-catalyzed cycloaddition of alkynes with 4-bromosydnones provides a convenient, mild, and regioselective method for the synthesis of a wide range of bromopyrazoles. The broad functional group tolerance of the cycloaddition reaction and further
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::554881289747b32ca3f65107937d1964
https://pubmed.ncbi.nlm.nih.gov/25636007
https://pubmed.ncbi.nlm.nih.gov/25636007
Autor:
Pierre Thuéry, Hervé Volland, Valentina Bevilacqua, Christophe Créminon, Sandra Gabillet, Manon Chaumonet, Marie-Claire Nevers, Julia Quinton, Sergii Kolodych, Frédéric Taran
Publikováno v:
ChemInform. 43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01a2216331871df1d490a8c1065fa6c3
https://doi.org/10.1002/chin.201243075
https://doi.org/10.1002/chin.201243075
Autor:
Sophie Dezard, Michael Carboni, Jean-Marie Gomis, Olivier Loreau, Frédéric Taran, Sandra Gabillet, Delphine Lecerclé
Publikováno v:
Organic letters. 9(20)
A simple and efficient method for constructing sulfur heterocycles was developed using a phosphine-catalyzed tandem umpolung addition and intramolecular cyclization of bifunctional sulfur pronucleophiles on arylpropiolates. The reaction offers a prom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f77da10c773662e436fd8faa372058e4
https://pubmed.ncbi.nlm.nih.gov/17803312
https://pubmed.ncbi.nlm.nih.gov/17803312
Autor:
Sandra Gabillet, Jean-Marie Gomis, Olivier Loreau, Delphine Lecercle, Sophie Dezard, Frédéric Taran
Publikováno v:
ChemInform. 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7df97094eb1ee3e8110de09719d4d6a
https://doi.org/10.1002/chin.200725151
https://doi.org/10.1002/chin.200725151