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Gökçe Merey

Researcher at Hittite University

Publications -  16
Citations -  492

Gökçe Merey is an academic researcher from Hittite University. The author has contributed to research in topics: Carbenoid & Diazo. The author has an hindex of 7, co-authored 16 publications receiving 428 citations. Previous affiliations of Gökçe Merey include Emory University & University of Maryland, College Park.

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Nucleotide, c-di-GMP, c-di-AMP, cGMP, cAMP, (p)ppGpp signaling in bacteria and implications in pathogenesis

TL;DR: An update of nucleotide signaling in bacteria is provided and it is shown how these signals intersect or integrate to regulate the bacterial phenotype and the chemical syntheses of the various nucleotide second messengers and the use of analogs thereof as antibiofilm or immune modulators are discussed.
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Nucleotide, c-di-GMP, c-di-AMP, cGMP, cAMP, (p)ppGpp Signaling in Bacteria and Implications in Pathogenesis

TL;DR: In this paper, the authors provide an update of nucleotide signaling in bacteria and show how these signals intersect or integrate to regulate the bacterial phenotype, and discuss the chemical syntheses of various nucleotide second messengers and the use of analogs thereof as antibiofilm or immune modulators.
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The rhodium(II) carbenoid cyclization–cycloaddition cascade of α-diazo dihydroindolinones for the synthesis of novel azapolycyclic ring systems

TL;DR: The power of the intramolecular cascade sequence is that it rapidly assembles a pentacyclic ring system containing three new stereocenters and two adjacent quaternary centers stereospecifically in a single step and in high yield.
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Utilization of the antiaromatic 2H-indol-2-one ring system for the synthesis of substituted spiro-oxindoles

TL;DR: The utility of the quasi-antiaromatic 2H-indol-2-one system for the synthesis of substituted oxindoles and spiro-oxindoles was investigated and it was found that it could be readily generated by treating a 3-hydroxy substituted 1,3-dihydroindol -2- one with a Lewis acid.
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N-O tethered carbenoid cyclopropanation facilitates the synthesis of a functionalized cyclopropyl-fused pyrrolidine.

TL;DR: A facile approach to a cyclopropyl-fused pyrrolidine, which contains four stereogenic centers, is reported by employing the N-O tethered carbenoid methodology, demonstrating the potential of this methodology for making cycloprostyl- fused heterocycles.