Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Raphaël Robiette"'
Publikováno v:
Journal of the American Society of Brewing Chemists. 81:23-32
Cysteinylated and glutathionylated precursors of sulfanylalkyl alcohols have been extensively studied in hop and grape matrices, in contrast to those of sulfanylalkyl aldehydes and sulfanylalkyl acetates. Here, cysteinylated and glutathionylated addu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::622b1e472e148c73c3e761deebfab58e
https://doi.org/10.1080/03610470.2021.2015560
https://doi.org/10.1080/03610470.2021.2015560
Publikováno v:
European Journal of Organic Chemistry, Vol. 2021, no.20, p. 2862-2868 (2021)
Vinylcyclopropanes are versatile intermediates in organic synthesis which undergo various rearrangements. We report a new rearrangement of vinylcyclopropane into skipped diene. A detailed mechanistic study revealed that this transformation involves r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d53e726bc296bc70861c9aeb81ce238
https://doi.org/10.1002/ejoc.202100430
https://doi.org/10.1002/ejoc.202100430
Autor:
Guillaume Berionni, Damien Mahaut, Lei Hu, Nikolay Tumanov, Laurent Collard, Raphaël Robiette, Johan Wouters
Publikováno v:
Dalton Transactions, Vol. 50, no.14, p. 4772-4777 (2021)
ortho-Substituted and unsymmetrical 9-phospha-triptycenes were synthesizedviatwo synthetic approaches involving densely functionalizedortho-halogenated triarylmethane or phosphine precursors.ortho-Substituents imposed a considerable steric shielding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e46b846752479be070c0bbc277d3264a
https://doi.org/10.1039/d1dt00816a
https://doi.org/10.1039/d1dt00816a
Autor:
Julien Caillé, Raphaël Robiette
Publikováno v:
Organic & Biomolecular Chemistry, (2021)
The stereocontrolled formation of medium-sized carbocycles is a major goal in modern organic chemistry due to their widespread occurrence in natural products and pharmaceutically active ingredients. One approach consists in the use of cycloaddition r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86cd1c5930906a7d082067b4ac1466ff
https://doi.org/10.1039/d1ob00838b
https://doi.org/10.1039/d1ob00838b
Publikováno v:
Institute of Brewing & Distilling. Brewing & Distilling Directory, Vol. 128, no.2, p. 43-51 (2022)
While cysteinylated (Cys-) and glutathionylated (G-) precursors of 3-sulfanylhexanol (3SHol) and 3-sulfanylpentanol (3SPol) appear to be ubiquitous in hop varieties, no data are available on precursors of their seven-carbon analogue 3-sulfanylheptano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6992e8c14ede6a8b5818df4477be3c9e
https://hdl.handle.net/2078.1/262543
https://hdl.handle.net/2078.1/262543
Autor:
Victor-Emmanuel Kassin, Isaline Jacquemin, Raphaël Robiette, Thomas Toupy, Jean-Christophe Monbaliu, Romain Morodo, Kristof Van Hecke
Publikováno v:
Green Chemistry, Vol. 23, no.6, p. 2336-2351 (2021)
The unique reactivity profile of α-chloronitroso derivatives is expressed to its fullest potential through the development of an integrated, modular and scalable continuous flow process for the electrophilic α-aminohydroxylation of various enolizab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22ff086325c9ef3d96f3a44a560903b3
https://hdl.handle.net/2078.1/245590
https://hdl.handle.net/2078.1/245590
Autor:
Stéphane P. Vincent, Abdellatif Tikad, Jérôme Cornil, Raphaël Robiette, Mathilde Vandamme, Christophe J.-M. Frédéric, Lidia Dumitrescu
Publikováno v:
Organic Letters, Vol. 20, no.21, p. 6769-6773 (2018)
Highly (Z)-diastereoselective approaches for the synthesis of trifluoromethylated exo-glycals by copper and photoredox catalysis are described. These complementary reactions are applicable to a wide range of methylene exo-glycals generated from the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e6d1b390b695c9cb919415024c0b383
https://doi.org/10.1021/acs.orglett.8b02891
https://doi.org/10.1021/acs.orglett.8b02891
Autor:
Mario Waser, Yang Fan, Steven R. Kass, Maximilian Tiffner, Raphaël Robiette, Johannes Schörgenhumer
Publikováno v:
The Journal of Organic Chemistry, Vol. 83, no.17, p. 9991-10000 (2018)
Cycloadditions of epoxides with CO2 to synthesize cyclic five-membered ring organic carbonates are of broad interest from a synthetic, environmental, and green chemistry perspective, and the development of effective catalysts for these transformation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c94d02a2c03b81ce8128abe5db1f3b19
https://doi.org/10.1021/acs.joc.8b01374
https://doi.org/10.1021/acs.joc.8b01374
Autor:
Trieu-Van Tran, Soumia El Aakchioui, Sébastien Clergue, Olivier Rousseau, Geoffroy Dequirez, Raphaël Robiette, Gabriella Barozzino-Consiglio, Thierry Delaunay
Publikováno v:
Chemistry-A European Journal, Vol. 24, no.44, p. 11417-11425 (2018)
A formal [4+1]-annulation strategy between sulfur ylides and 1,3-dienes was developed to afford functionalized cyclopentanoids. The process consists of a stereoselective cyclopropanation reaction followed, in situ, by a stereospecific MgI2 -catalyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61f5fdb711dc505745afd65e4c3e409a
https://doi.org/10.1002/chem.201801874
https://doi.org/10.1002/chem.201801874
Publikováno v:
The Journal of Organic Chemistry, Vol. 84, no.17, p. 11268-11274 (2019)
Two practical and high-yielding syntheses of 9-phosphatriptycene are reported. In both approaches, the key step is based on the cyclization of a (tris)lithio-triphenylmethane or a (tris)lithio-triphenylphosphine intermediate on a phosphorus or a carb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35a283b6a51bbf02d166b3152cb1a7c1
https://pubmed.ncbi.nlm.nih.gov/31385508
https://pubmed.ncbi.nlm.nih.gov/31385508