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Maciej A. Walczak

Researcher at University of Warsaw

Publications -  83
Citations -  2351

Maciej A. Walczak is an academic researcher from University of Warsaw. The author has contributed to research in topics: Nucleophile & Chemistry. The author has an hindex of 23, co-authored 70 publications receiving 1767 citations. Previous affiliations of Maciej A. Walczak include Adam Mickiewicz University in Poznań & University of Colorado Boulder.

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Combined measurements of Higgs boson couplings in proton–proton collisions at √s=13Te

Albert M. Sirunyan, +2268 more
TL;DR: Combined measurements of the production and decay rates of the Higgs boson, as well as its couplings to vector bosons and fermions, are presented and constraints are placed on various two Higgs doublet models.
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Search for Narrow Resonances in Dijet Final States at sqrt[s]=8 TeV with the Novel CMS Technique of Data Scouting.

Vardan Khachatryan, +2245 more
TL;DR: A search for narrow resonances decaying into dijet final states is performed on data from proton-proton collisions at a center-of-mass energy of 8 TeV, corresponding to an integrated luminosity of 18.8 fb^{-1}.
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Inclusive Search for a Highly Boosted Higgs Boson Decaying to a Bottom Quark-Antiquark Pair

Albert M. Sirunyan, +2226 more
TL;DR: An inclusive search for the standard model Higgs boson produced with large transverse momentum (p_{T}) and decaying to a bottom quark-antiquark pair (bb[over ¯]) is performed using a data set of pp collisions collected with the CMS experiment at the LHC.
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Highly Stereospecific Cross-Coupling Reactions of Anomeric Stannanes for the Synthesis of C-Aryl Glycosides

TL;DR: It is demonstrated that configurationally stable anomeric stannanes undergo a stereospecific cross-coupling reaction with aromatic halides in the presence of a palladium catalyst with exceptionally high levels of stereocontrol.
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Glycosyl Cross-Coupling of Anomeric Nucleophiles: Scope, Mechanism, and Applications in the Synthesis of Aryl C-Glycosides

TL;DR: In this article, a novel approach to stereoselective synthesis of C-aryl glycosides capitalizing on the highly stereospecific reaction of anomeric nucleophiles was described.