G
Grigoriy Ya. Remennikov
Researcher at Ludwig Maximilian University of Munich
Publications - 8
Citations - 691
Grigoriy Ya. Remennikov is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: Aryl & Carbocation. The author has an hindex of 4, co-authored 8 publications receiving 646 citations.
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Journal ArticleDOI
Reference Scales for the Characterization of Cationic Electrophiles and Neutral Nucleophiles
Herbert Mayr,Thorsten Bug,Matthias F. Gotta,Nicole Hering,Bernhard Irrgang,Brigitte Janker,Bernhard Kempf,Robert Loos,Armin R. Ofial,Grigoriy Ya. Remennikov,Holger Schimmel +10 more
TL;DR: Mayr et al. as discussed by the authors used correlation analysis to determine the electrophilicity parameters E and N and s as defined by the equation log k(20 °C) = s(N + E).
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Switching between penta- and hexacoordination with salen-silicon-complexes
Jörg Wagler,Uwe Böhme,Erica Brendler,B. Thomas,Sigrid Goutal,Herbert Mayr,Bernhard Kempf,Grigoriy Ya. Remennikov,Gerhard Roewer +8 more
TL;DR: The reaction between phenyltrichlorosilane and tetradentate ligands, supported by an amine base, yields pentacoordinate silicon complexes (C6H5)Si as discussed by the authors, which can be transferred onto various ligands of 2-iminomethylphenolate type.
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5‐Methoxyfuroxano[3,4‐d]pyrimidine: a highly reactive neutral electrophile
TL;DR: In this article, the second-order rate constants of 6.7-dihydro-5-methoxyfuroxano[3,4-d]pyrimidines were derived for nucleophiles of N ≥ 3.37.
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Kinetics of the Reactions of Flavylium Ions with π-Nucleophiles
TL;DR: In this article, the kinetics of the reactions of the flavylium ion 1a and the 4′-methoxyflavylium ions 1b with various π-nucleophiles and tributylstannane were investigated photometrically in dichloromethane.
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Synthesis of Condensed Heterocycles, Containing Partially Saturated Pyrimidine Nuclei, from Aromatic Pyrimidine Derivatives
TL;DR: In this article, the authors summarized current developments in the preparation of condensed heterocycles containing dihydropyrimidine and tetrahydropyridine nuclei by various transformations of preexisting aromatic pyrimidine derivatives and presented a variety of strategies for the construction of these highly functional heterocyclic systems.