Publications Sébastien

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[29] Regio- and Chemioselective Double Allylic Substitution of Alkenyl vic-diols
Chen, B.; Pagès, L.; Dollet, R.; Kouklovsky, C.; Prévost, S.; de la Torre, A.
Org. Lett.2024, doi: 10.1021/acs.orglett.4c00495.


[28] Palladium-Catalyzed C8-Fluoroalkylation and C8-Fluoroalkenylation of Naphthalenes by C-H activation
Amistadi-Revol, H.; Tremblais, J.; Casaretto, N.; Prévost, S.
Eur. J. Org. Chem. 2024, doi: 10.1002/ejoc.202400194.


[27] Synthesis of naphtholactams and their biological evaluation against Pseudomonas aeruginosa
Amistadi-Revol, H.;" Baëtz, B.;" Liu, S.;" Giraud, C.; Prévost, S.
Arkivoc 2024,202312091.


[26] C-H Functionalization of Aldehydes and Ketones with Transient Directing Groups: Recent Developments
Amistadi-Revol, H.;" Liu, S.;" Prévost, S.
Eur. J. Org. Chem. 2023, 26, e202300582.


[25] Palladium-Catalyzed Regioselective peri- and ortho-Halogenation of 1-Naphthaldehydes: Application to the Synthesis of Polycyclic Natural Product Skeletons
Amistadi-Revol, H.; Garrec, J.; Casaretto, N.; Prévost, S.
Eur. J. Org. Chem. 2023, 26, e202300359.


[24] Palladium-Catalyzed ortho-C-H Alkoxycarbonylation of Aromatic Aldehydes via a Transient Directing Group Strategy
Liu. S.; Prévost, S.
Org. Lett. 2023, 25, 1380-1385.


[23] Palladium-Catalyzed C8-Oxygenation of Naphthalene Derivatives: Direct Access to Naphtholactone Skeleton
Berrou, C.; Prévost, S.
Adv. Synth. Catal. 2021, 363, 4091-4095.


[22] Synthesis of 2-phosphonoheterocylces via base-promoted 5-endo cyclization
Bousbia, A.; Benkhoud, M. L.; El-Kaïm, L.; Prévost, S.
Tetrahedron Letters 2021, 64, 152742.


[21] Regioselective C-H Functionalization of Naphthalenes: Reactivity and Mechanistic Insights
Prévost, S.
Chem. Plus Chem. 2020, 85, 476-486 (invited review).


[20] Palladium-Catalyzed C8-Arylation of Naphthalenes through C-H Activation: a Combined Experimental and Computational Study
Garrec, J.; Cordier, M.; Frison, G.; Prévost, S.
Chem. Eur. J. 201925, 14441-14446 (selected as Hot Paper).
Highlighted in: Synfacts 2020, 16, 155.


[19] Progress toward the total synthesis of mirabalin isomers
Echeverria, P.-G.; Pons, A.; Prévost, S.; Férard, C.; Cornil, J.; Guérinot, A.; Cossy, J.; Phansavath, P.; Ratovelomanana-Vidal, V.
Arkivoc 2019,  44-68.


[18] Azetidine‐Containing Alkaloids Produced by a Quorum‐Sensing‐ Regulated Nonribosomal Peptide Synthetase Pathway in Pseudomonas aeruginosa
Hong, Z.; Bolard, A.; Giraud, C.; Prévost, S.; Genta-Jouve, G.; Deregnaucourt, C.; Häussler, S.; Jeannot, K.; Li, Y.
Angew. Chem. Int. Ed. 2019, 58, 3178-3182.


[17] Palladium triggered diene formation from nitro allylic compounds: a versatile entry into naphthalene derivatives
Kerim, M. D.; Jia, S.; Theodorakidou, C.; Prévost, S.; El Kaïm, L.
Chem. Commun. 2018, 54, 10917-10920.


[16] Multifaceted study on a cytochalasin scaffold: lessons on reactivity, multidentate catalysis and anticancer properties
Zaghouani, M.; Gayraud, O.; Jactel, V.; Prévost, S.; Dezaire, A.; Sabbah, M.; Escargueil, A.; Lai, T.-L.; Le Clainche, C.; Rocques, N.; Romero, S.; Gautreau, A.; Blanchard, F.; Frison, G.; Nay, B.
Chem. Eur. J. 2018, 24, 16686-16691.


[15] Reoptimization of the Organocatalyzed Double Aldol Domino Process to a Key Enal Intermediate and Its Application to the Total Synthesis of D12-Prostaglandin J3
Pelss, A.; Handhamsetty, N.; Smith, J. R.; Mailhol, D.; Silvi, M.; Watson, A. J. A.; Perez-Powell, I.; Prévost, S.; Schützenmeister, N.; Moore, P. R.; Aggarwal, V. K.
Chem. Eur. J. 2018, 24, 9542-9545.
Highlighted in Synfacts: Synfacts 2018, 14, 892.

[14] Intramolecular Aryne-Furan Cycloadditions for the Synthesis of Anticancer Naphthalimides
Prévost, S.; Dezaire, A.; Escargueil, A.
J. Org. Chem. 2018, 83, 4871-4881.


[13] Activation of Olefins via Asymmetric Brønsted Acid Catalysis
Tsuji, N.; Kennemur, J. L.; Buyck, T.; Lee, S.; Prévost, S.; Kaib, P. S. J.; Bykov, D.; Farès, C.; List, B.
Science 2018, 359, 1501-1505.
Highlighted in Synfacts: Synfacts 2018, 14, 757.


[12] Bioinspired Adventures in Total Synthesis of Mixed Polyketide-Nonribosomal Peptide Natural Products
Nay, B.; Zaghouani, M.; Laroche, B.; Prévost, S.; Li, X.-W.; Ear, A.; Riache, N.
In Strategies and Tactics in Organic Synthesis; Harmata, M., Ed.; Elsevier Academic Press Inc, 2017; Vol. 13, pp. 55-80.


[11] Synthesis of Prostaglandin Analogues, Latanoprost and Bimatoprost Using Organocatalysis via a Key Bicyclic Enal Intermediate
Prévost, S.; Thai, K.; Schützenmeister, N.; Coulthard, G.; Erb, W.; Aggarwal, V. K.
Org. Lett. 2015, 17, 504-507.
Selected for ACS Select Virtual Issue on Organocatalysis: ACS Catal. 2015, 5, 6980-6988.


[10] Catalytic Asymmetric Synthesis of Thiols
Monaco, M. R.; Prévost, S.; List, B.
J. Am. Chem. Soc. 2014, 136, 16982-16985.
Highlighted in Synfacts: Synfacts 2015, 11, 326.


[9] Catalytic Asymmetric Torgov Cyclization: A Concise Total Synthesis of (+)-Estrone
Prévost, S.; Dupré, N.; Leutzsch, M.; Wang, Q.; Wakchaure, V.; List, B.
Angew. Chem. Int. Ed. 2014, 53, 8770-8773.
Highlighted in Synfacts: Synfacts 2014, 10, 1212.


[8] Organocatalytic Asymmetric Hydrolysis of Epoxides
Monaco, M. R.; Prévost, S.; List, B.
Angew. Chem. Int. Ed. 2014, 53, 8142-8145.
Highlighted in Synfacts: Synfacts 2014, 10, 986.


[7] Synthetic Strategy Toward the C44-C65 Fragment of Mirabalin
Echeverria, P.-G.; Prévost, S.; Cornil, J.; Ferard, C.; Reymond, S.; Guérinot, A.; Cossy, J.; Ratovelomanana-Vidal, V.; Phansavath, P.
Org. Lett. 2014, 16, 2390-2393.


[6] DIFLUORPHOS and SYNPHOS in asymmetric catalysis : Synthetic applications
Prévost, S.; Ayad, T.; Genêt, J.-P.; Phansavath, P.; Vidal, V.
J. Chem. Sci. 2014, 126, 325-340.


[5] Palladium-Catalyzed Allylic Alkylation of Allyl Dienol Carbonates: Reactivity, Regioselectivity, Enantioselectivity and Synthetic Applications
Arseniyadis, S.; Fournier, J.; Saravanan, T.; Lozano, O.; Prévost, S.; Archambeau, A.; Menozzi, C.; Cossy, J.
Synlett 2013, 2350-2364.


[4] Lyngbouilloside and Related Macrolides from Marine Cyanobacteria
ElMarrouni, A.; Kolleth, A.; Lebeuf, R.; Gebauer, J.; Prévost, S.; Heras, M.; Arseniyadis, S.; Cossy, J.
Nat. Prod. Commun. 2013, 8, 965-972.


[3] Total Synthesis of Symbioramide: a Flexible Approach for the Efficient Preparation of Structural Isomers
Prévost, S.; Ayad, T.; Phansavath, P.; Vidal, V.
Adv. Synth. Catal. 2011, 353, 3213-3226.


[2] Dynamic kinetic resolution of α-chloro β-keto esters and phosphonates: hemisynthesis of Taxotere® through Ru-DIFLUORPHOS asymmetric hydrogenation
Prévost, S.; Gauthier, S.; Cano de Andrade, M.C.; Mordant, C.; Touati, A.R.; Lesot, P.; Savignac, P.; Ayad, T.; Phansavath, P.; Ratovelomanana-Vidal, V.; Genêt, J.-P.
Tetrahedron: Asymmetry 2010, 21, 1436-1446.


[1] A stereoselective synthesis of (+)-L-733,060 from ethyl (R)-(+)-2,3-epoxypropanoate
Prévost, S.; Phansavath, P.; Haddad, M.
Tetrahedron: Asymmetry 2010, 21, 16-20.


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