Emmanuel Roulland, PhD

Affiliations: 
2005-2012 ICSN-CNRS CNRS Gif sur Yvette France, Gif-sur-Yvette, Île-de-France, France 
 2012-2017 UMR 8638 CNRS Universite Paris Descartes, Paris, Île-de-France, France 
Area:
Total Synthesis of Natural Products and Organometallic Chemistry
Website:
http://www.comete.cnrs.fr/index.php/equipes/10-synthese-totale-et-chimie-organometallique/22-dr-emmanuel-roulland
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Publications

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Tresse C, François-Heude M, Servajean V, et al. (2021) Total Synthesis of Tiacumicin B: Study of the Challenging β-Selective Glycosylations. Chemistry (Weinheim An Der Bergstrasse, Germany)
Aimond A, Calabro K, Audoin C, et al. (2020) Cytotoxic and Anti-Inflammatory Effects of -Kaurane Derivatives Isolated from the Alpine Plant . Molecules (Basel, Switzerland). 25
Norsikian S, Tresse C, François-Eude M, et al. (2020) Total Synthesis of Tiacumicin B: Implementing H-bond-Directed Acceptor Delivery for Highly Selective β-Glycosylations. Angewandte Chemie (International Ed. in English)
Jeanne-Julien L, Masson G, Kouoi R, et al. (2019) Stereoselective Access to ( E)-1,3-Enynes through Pd/Cu-Catalyzed Alkyne Hydrocarbation of Allenes. Organic Letters
Roulland E, Solanki H, Calabro K, et al. (2018) Stereochemical Study of Puna'auic Acid, an Allenic Fatty Acid from the Eastern Indo-Pacific Cyanobacterium Pseudanabaena sp. Organic Letters
Jeanne-Julien L, Astier E, Lai-Kuen R, et al. (2018) Palladium Nanoparticle-Catalyzed Stereoretentive Cross-Coupling of Alkenyl Sulfides with Grignard Reagents. Organic Letters
Roulland E. (2018) Tiacumicin B: An Antibiotic of Prime Importance and a Natural Product with an Inspiring Complex Structure Synthesis. 50: 4189-4200
Jeanne-Julien L, Masson G, Astier E, et al. (2017) Study of the Construction of the Tiacumicin B Aglycone. The Journal of Organic Chemistry
Jeanne-Julien L, Masson G, Astier E, et al. (2017) Synthesis of a Tiacumicin B Protected Aglycone. Organic Letters
Caumes X, Jeanne-Julien L, Khelifi C, et al. (2016) Diastereoselective synthesis of 2,5-disubstituted-3-hydroxy-tetrahydrofurans through a counterion-directed Tsuji–Trost reaction Organic Chemistry Frontiers. 3: 1462-1466
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