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Xavier Moreau
Researcher at Université Paris-Saclay
Publications - 130
Citations - 1978
Xavier Moreau is an academic researcher from Université Paris-Saclay. The author has contributed to research in topics: Enantioselective synthesis & Catalysis. The author has an hindex of 22, co-authored 120 publications receiving 1726 citations. Previous affiliations of Xavier Moreau include University of Bordeaux & University of Manchester.
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Journal ArticleDOI
Macrolactonizations in the Total Synthesis of Natural Products
Journal ArticleDOI
Update 1 of: macrolactonizations in the total synthesis of natural products.
TL;DR: Products A. Parenty,† X. Moreau,†,§ Gilles Niel,‡ and J.-M.
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Gold‐ and Platinum‐Catalyzed Cycloisomerization of Enynyl Esters versus Allenenyl Esters: An Experimental and Theoretical Study
Nicolas Marion,Gilles Lemière,Andrea Correa,Chiara Costabile,Rubén S. Ramón,Xavier Moreau,Pierre de Frémont,Rim Dahmane,Alexandra Hours,Denis Lesage,Jean-Claude Tabet,Jean-Philippe Goddard,Vincent Gandon,Luigi Cavallo,Louis Fensterbank,Max Malacria,Steven P. Nolan,Steven P. Nolan +17 more
TL;DR: It is shown that bicyclo[3.1.0]hexene 5 is likely formed by a 1,3-OAc shift/allene-ene cyclization/1,2-Oac shift sequence, as calculated by DFT and supported by Au-catalyzed cyclization of isolated allenenyl acetate 7, which leads to improved selectivity in the formation of 5.
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Catalytic and asymmetric vinylogous mukaiyama reactions on aliphatic ketones: formal asymmetric synthesis of taurospongin a.
TL;DR: Catalytic asymmetric vinylogous Mukaiyama reactions on ketones, leading to the formation of alpha,beta-unsaturated lactones with tertiary alcohols, have been described and applied in a formal enantioselective synthesis of taurospongin A.
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Merging oxidative dearomatization and aminocatalysis: one-pot enantioselective synthesis of tricyclic architectures.
Francois Portalier,Flavien Bourdreux,Jerome Marrot,Xavier Moreau,Vincent Coeffard,Christine Greck +5 more
TL;DR: The combination of oxidative dearomatization and trienamine/enamine activation in a single vessel generates functionalized tricyclic architectures with up to six contiguous stereocenters with excellent stereoselectivities from readily available planar substrates.