Gaelle Chouraqui

Affiliations: 
iSm2 
Area:
Organic Chemistry
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"Gaelle Chouraqui"
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Publications

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Abdou-Mohamed A, Aupic C, Fournet C, et al. (2023) Stereoselective formation of boron-stereogenic organoboron derivatives. Chemical Society Reviews. 52: 4381-4391
Aupic C, Abdou Mohamed A, Figliola C, et al. (2019) Highly diastereoselective preparation of chiral NHC-boranes stereogenic at the boron atom. Chemical Science. 10: 6524-6530
Rodier F, Rajzmann M, Parrain JL, et al. (2013) Diastereoselective access to polyoxygenated polycyclic spirolactones through a rhodium-catalyzed [3+2] cycloaddition reaction: experimental and theoretical studies. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 2467-77
Bartoli A, Chouraqui G, Parrain JL. (2012) Collective domino approach toward the core of molecules isolated from the genus Schisandra. Organic Letters. 14: 122-5
Sridharan V, Vologdin N, Virolleaud MA, et al. (2011) Consecutive reactions with sulfoximines: Straightforward synthesis of substituted 5,5-spiroketals Synthesis. 2085-2090
Virolleaud MA, Sridharan V, Mailhol D, et al. (2009) Consecutive reactions with sulfoximines: a direct access to 2-sulfonimidoylylidene tetrahydrofurans and 6-sulfonimidoylmethyl-3,4-dihydro-2H-pyrans Tetrahedron. 65: 9756-9764
Paterson I, Ashton K, Britton R, et al. (2008) Total synthesis of (-)-reidispongiolide A, an actin-targeting macrolide isolated from the marine sponge Reidispongia coerulea. Chemistry, An Asian Journal. 3: 367-87
Paterson I, Ashton K, Britton R, et al. (2007) Total synthesis of (-)-reidispongiolide A, an actin-targeting marine macrolide. Angewandte Chemie (International Ed. in English). 46: 6167-71
Petit M, Chouraqui G, Aubert C, et al. (2007) Regioselective preparation of tetrasubstituted alkenes from ketones using Krief's methodology as a key step for a straightforward synthesis of dienynes Arkivoc. 2007: 278-291
Chouraqui G, Petit M, Phansavath P, et al. (2006) From an acyclic, polyunsaturated precursor to the polycyclic taxane ring system: The [4+2]/[2+2+2] and [2+2+2]/[4+2] cyclization strategies European Journal of Organic Chemistry. 1413-1421
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