François-hugues Porée
Affiliations: | Université de Cergy-Pontoise |
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Parents
Sign in to add mentorJanick Ardisson | grad student | 2003 | Université de Cergy-Pontoise | |
(Vers la synthèse totale du (+)-discodermolide nouvel antitumoral stabilisant du fuseau) | ||||
Ange Pancrazi | grad student | 2003 | Université de Cergy-Pontoise | |
(Vers la synthèse totale du (+)-discodermolide nouvel antitumoral stabilisant du fuseau) |
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Publications
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Alleman C, Gadais C, Legentil L, et al. (2023) Strategies to access the [5-8] bicyclic core encountered in the sesquiterpene, diterpene and sesterterpene series. Beilstein Journal of Organic Chemistry. 19: 245-281 |
Le Roch M, Afonso D, Chirkin E, et al. (2022) Structure simplification of the Securinine skeleton reveals the importance of BCD ring system for the cytotoxic activity on HCT116 and HL60 cell lines. Bioorganic & Medicinal Chemistry. 58: 116658 |
Chirkin E, Bouzidi C, Porée F. (2019) Tungsten-Promoted Hetero-Pauson–Khand Cycloaddition: Application to the Total Synthesis of (–)-Allosecurinine Synthesis. 51: 2001-2006 |
Menelle P, Cottet K, Fromentin Y, et al. (2017) Progress on PPAPs cyclization: Guttiferone A as a case study Tetrahedron Letters. 58: 4876-4879 |
Markovi D, Porée F. (2016) Editorial (Thematic Issue: Diels-Alder Reaction (Part 2)) Current Organic Chemistry. 20: 2283-2283 |
Markovic D, Porée F. (2016) Editorial (Thematic Issue: Diels-Alder Reaction (Part 1)) Current Organic Chemistry. 20: 2135-2135 |
Chirkin E, Michel S, Porée FH. (2015) Viability of a [2 + 2 + 1] Hetero-Pauson-Khand Cycloaddition Strategy toward Securinega Alkaloids: Synthesis of the BCD-Ring Core of Securinine and Related Alkaloids. The Journal of Organic Chemistry. 80: 6525-8 |
Chirkin E, Atkatlian W, Porée FH. (2015) The Securinega alkaloids. The Alkaloids. Chemistry and Biology. 74: 1-120 |
Chirkin E, Atkatlian W, Do Q, et al. (2015) Chiroptical study and absolute configuration of securinine oxidation products. Natural Product Research. 29: 1235-42 |
Marković D, Kolympadi M, Deguin B, et al. (2015) The isolation and synthesis of neodolastane diterpenoids. Natural Product Reports. 32: 230-55 |