M
Maud Reiter
Researcher at University of Oxford
Publications - 21
Citations - 384
Maud Reiter is an academic researcher from University of Oxford. The author has contributed to research in topics: Aldol reaction & Catalysis. The author has an hindex of 9, co-authored 20 publications receiving 347 citations. Previous affiliations of Maud Reiter include Merck & Co. & Princeton University.
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Journal ArticleDOI
The organocatalytic three-step total synthesis of (+)-frondosin B
TL;DR: A combination of X-ray crystallographic data, deuterium labeling, and chemical correlation studies provides further evidence as to the correct absolute stereochemical assignment of (+)-frondosin B.
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Microscale High-Throughput Experimentation as an Enabling Technology in Drug Discovery: Application in the Discovery of (Piperidinyl)pyridinyl-1H-benzimidazole Diacylglycerol Acyltransferase 1 Inhibitors
Tim Cernak,Nathan J. Gesmundo,Kevin D. Dykstra,Yang Yu,Zhicai Wu,Zhi-Cai Shi,Petr Vachal,Donald M. Sperbeck,Shuwen He,Beth Ann Murphy,Lisa M. Sonatore,Steven Williams,Maria Madeira,Andreas Verras,Maud Reiter,Claire Lee,James Cuff,Edward C. Sherer,Jeffrey T. Kuethe,Stephen D. Goble,Nicholas Perrotto,Shirly Pinto,Dong-Ming Shen,Ravi P. Nargund,James M. Balkovec,Robert J. DeVita,Spencer D. Dreher +26 more
TL;DR: The application of miniaturized high-throughput experimentation methods to resolve synthetic chemistry challenges on the frontlines of a lead optimization effort to develop diacylglycerol acyltransferase (DGAT1) inhibitors is demonstrated.
Journal ArticleDOI
Biocatalytic Approaches to Hetero‐Diels–Alder Adducts of Carbonyl Compounds
Veronique Gouverneur,Maud Reiter +1 more
TL;DR: This work has shown that a conceptually novel biocatalytic approach to hetero-Diels-Alder (HDA) adducts derived from carbonyl dienophiles has been developed mirroring a stepwise aldol Michael mechanism instead of a concerted pathway, and is best applied for the preparation of enantioenriched HDA adduction derived from poorly electrophilic acceptors.
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Palladium-Catalyzed Oxidative Cyclizations: Synthesis of Dihydropyranones and Furanones
TL;DR: The sole product of the oxidative cyclization of alpha,beta-dihydroxyenone was a five-membered furan-3(2H)-one derivative, suggesting that the ring closure of these diols is both chemo- and regioselective.
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Intramolecular Hetero-Michael Addition of β-Hydroxyenones for the Preparation of Highly Substituted Tetrahydropyranones
TL;DR: Experimental results suggest that C=O coordination was the preferred mode of activation for reactions performed in the presence of Al(ClO(4) x 9 H(2)O or [Pd(MeCN)(4)](BF(4))(2), and this catalyst can promote enolisation.