D
Dmitrii S. Yufit
Researcher at Durham University
Publications - 104
Citations - 1459
Dmitrii S. Yufit is an academic researcher from Durham University. The author has contributed to research in topics: Pyridine & Nucleophilic aromatic substitution. The author has an hindex of 22, co-authored 102 publications receiving 1384 citations. Previous affiliations of Dmitrii S. Yufit include University of Göttingen.
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Journal ArticleDOI
Palladium-Catalyzed C−F Activation of Polyfluoronitrobenzene Derivatives in Suzuki−Miyaura Coupling Reactions
Matthew R. Cargill,Graham Sandford,Andrezj J. Tadeusiak,Dmitrii S. Yufit,Judith A. K. Howard,Pinar Kilickiran,Gabrielle Nelles +6 more
TL;DR: Investigations into the regioselectivity and reactivity of several tetrafluoro- and trifluoronitrobenzene derivatives provides further evidence for the highly nucleophilic character of the oxidative addition step in contrast to the concerted mechanism of more conventional Suzuki-Miyaura coupling reactions involving aryl iodides and bromides.
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The CF bond as a tool in the conformational control of amides
Caroline R.S. Briggs,Caroline R.S. Briggs,David O'Hagan,Judith A. K. Howard,Dmitrii S. Yufit +4 more
TL;DR: In this paper, the authors demonstrate the predictive power of using the CF bond as a tool in influencing the conformation of amides and peptides, and demonstrate that it is possible to predict solid state conformation for amides.
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Tetrahydropyrido[3,4-b]pyrazine scaffolds from pentafluoropyridine.
TL;DR: The potential of the polyfluorinated ring fused pyridine system as a scaffold for the synthesis of previously inaccessible poly-substituted pyridopyrazine derivatives is demonstrated, in which low molecular weight, polyfunctional heterocyclic derivatives are playing an increasingly important role.
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Polyhalogenated heterocyclic compounds. Macrocycles from perfluoro-4-isopropylpyridine.
Richard D. Chambers,Philip R. Hoskin,Alan R. Kenwright,Ali Kh. Khalil,Paul Richmond,Graham Sandford,Dmitrii S. Yufit,Judith A. K. Howard +7 more
TL;DR: In this article, a two-step synthesis of a variety of macrocyclic systems bearing pyridine sub-units was described by X-ray crystallography, and it was shown that complexation of either cations and anions is possible depending on the structure of the macrocycle.
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The First Enantiomerically Pure Triangulane (M)‐Trispiro[2.0.0.2.1.1]nonane Is a σ‐[4]Helicene
Armin de Meijere,Alexander F. Khlebnikov,Rafael R. Kostikov,Sergei I. Kozhushkov,Peter R. Schreiner,Alexander Wittkopp,Dmitrii S. Yufit +6 more
TL;DR: In this article, the first σ-bond analogue of the aromatic [n]helicenes, (M)-1, has been shown to have a remarkably high specific rotation, even at 589 nm, and it has no chromophore that would lead to significant absorption above 200 nm.