Zobrazeno 1 - 10
of 288
pro vyhledávání: '"Bezhan CHANKVETADZE"'
Autor:
Naomi KNAVS, Andreea ZUBAŞ, Georgiana APOSTOL, Christophe FURMAN, Adrian Sorin NICA, Bezhan CHANKVETADZE, Alina GHINET, Emmanuelle LIPKA
Publikováno v:
Journal of Chromatography Open, Vol 5, Iss , Pp 100129- (2024)
Eleven polysaccharide-based chiral stationary phases were screened to separate stereoisomers of six lactam derivatives by supercritical fluid chromatography (SFC). Those molecules are antagonists of the P2×7 receptor with potential anti-inflammatory
Externí odkaz:
https://doaj.org/article/868d52519edd4a5aa8bb00a9fd5ac45f
Autor:
Roberto Dallocchio, Alessandro Dessì, Barbara Sechi, Bezhan Chankvetadze, Sergio Cossu, Victor Mamane, Emmanuel Aubert, Carla Rozzo, Giuseppe Palmieri, Ylenia Spissu, Paola Peluso
Publikováno v:
Journal of Chromatography Open, Vol 2, Iss , Pp 100030- (2022)
In the last few years, chiral 4,4′-bipyridine derivatives have been developed for different applications in catalysis, enantioseparation science, supramolecular and theoretical chemistry by modulating the activity of the molecular system through th
Externí odkaz:
https://doaj.org/article/c2d5b6ddcb9d481e8c71f7a1c707ae75
Autor:
Bezhan Chankvetadze, Salvatore Fanali
Publikováno v:
Journal of Chromatography Open, Vol 2, Iss , Pp 100040- (2022)
Externí odkaz:
https://doaj.org/article/d923fd5c895449359497ac0d544d84a9
Autor:
Paola Peluso, Alessandro Dessì, Roberto Dallocchio, Barbara Sechi, Carlo Gatti, Bezhan Chankvetadze, Victor Mamane, Robin Weiss, Patrick Pale, Emmanuel Aubert, Sergio Cossu
Publikováno v:
Molecules, Vol 26, Iss 1, p 221 (2021)
The chalcogen bond (ChB) is a noncovalent interaction based on electrophilic features of regions of electron charge density depletion (σ-holes) located on bound atoms of group VI. The σ-holes of sulfur and heavy chalcogen atoms (Se, Te) (donors) ca
Externí odkaz:
https://doaj.org/article/82dfe9fa896d4b9c9f83133b07d7cad5
Autor:
Kenan Can Tok, Mehmet Gumustas, Giorgi Jibuti, Halit Sinan Suzen, Sibel A. Ozkan, Bezhan Chankvetadze
Publikováno v:
Molecules, Vol 25, Iss 24, p 5865 (2020)
In a recent study, opposite enantiomer elution order was observed for ketoprofen enantiomers on two amylose-phenylcarbamate-based chiral columns with the same chemical composition of the chiral selector but in one case with coated while in the other
Externí odkaz:
https://doaj.org/article/655da5fa64654fe18baba9488d9b8353
Autor:
Paola Peluso, Bezhan Chankvetadze
Publikováno v:
Chemical Reviews. 122:13235-13400
It is not a coincidence that both chirality and noncovalent interactions are ubiquitous in nature and synthetic molecular systems. Noncovalent interactivity between chiral molecules underlies enantioselective recognition as a fundamental phenomenon r
Autor:
Paola Peluso, David Landy, Lamia Nakhle, Roberto Dallocchio, Alessandro Dessì, Sulaiman Krait, Antonio Salgado, Bezhan Chankvetadze, Gerhard K.E. Scriba
Publikováno v:
Carbohydrate Polymers. 313:120870
Autor:
Alessandro Dessì, Barbara Sechi, Roberto Dallocchio, Bezhan Chankvetadze, Mireia Pérez‐Baeza, Sergio Cossu, Victor Mamane, Patrick Pale, Paola Peluso
Publikováno v:
Chirality (N.Y.N.Y., Online) (2022). doi:10.1002/chir.23417
info:cnr-pdr/source/autori:Alessandro Dessì, Barbara Sechi, Roberto Dallocchio, Bezhan Chankvetadze, Mireia Pérez-Baeza, Sergio Cossu, Victor Mamane, Patrick Pale, Paola Peluso/titolo:Comparative enantioseparation of planar chiral ferrocenes on polysaccharide-based chiral stationary phases/doi:10.1002%2Fchir.23417/rivista:Chirality (N.Y.N.Y., Online)/anno:2022/pagina_da:/pagina_a:/intervallo_pagine:/volume
Dessì, Alessandro Sechi, Barbara Dallocchio, Roberto Chankvetadze, Bezhan Pérez Baeza, Mireia Cossu, Sergio Mamane, Victor Pale, Patrick Peluso, Paola 2022 Comparative enantioseparation of planar chiral ferrocenes on polysaccharide-based chiral stationary phases. Chirality 34 4 609 619
info:cnr-pdr/source/autori:Alessandro Dessì, Barbara Sechi, Roberto Dallocchio, Bezhan Chankvetadze, Mireia Pérez-Baeza, Sergio Cossu, Victor Mamane, Patrick Pale, Paola Peluso/titolo:Comparative enantioseparation of planar chiral ferrocenes on polysaccharide-based chiral stationary phases/doi:10.1002%2Fchir.23417/rivista:Chirality (N.Y.N.Y., Online)/anno:2022/pagina_da:/pagina_a:/intervallo_pagine:/volume
Dessì, Alessandro Sechi, Barbara Dallocchio, Roberto Chankvetadze, Bezhan Pérez Baeza, Mireia Cossu, Sergio Mamane, Victor Pale, Patrick Peluso, Paola 2022 Comparative enantioseparation of planar chiral ferrocenes on polysaccharide-based chiral stationary phases. Chirality 34 4 609 619
Planar chiral ferrocenes are well-known compounds that have attracted interest for application in synthesis, catalysis, material science, and medicinal chemistry for several decades. In spite of the fact that asymmetric synthesis procedures for obtai
Autor:
Adham Ahmed, Jeanethe A. Anguizola, Katia Arena, Sanka N. Atapattu, Juan José Baeza-Baeza, Kimber L. Barnett, Bogusław Buszewski, Francesco Cacciola, Andrea Carotti, Martina Catani, Alberto Cavazzini, Bezhan Chankvetadze, G. D’Orazio, John W. Dolan, Paola Dugo, Filip Duša, C. Fanali, Salvatore Fanali, Tivadar Farkas, Attila Felinger, František Foret, T. Fornstedt, P. Forssén, María Celia García-Alvarez-Coque, Timothy W. Graul, Paul R. Haddad, David S. Hage, Brent Harrington, Srishti Joshi, Malte Kaspereit, Julia Kuligowski, Margaret E. LaCourse, William R. LaCourse, Fernando Mauro Lanças, Bernhard Lendl, Rong Li, Edvaldo Vasconcelos Soares Maciel, Ryan Matsuda, Sven W. Meckelmann, Laura Mercolini, Luigi Mondello, José Antonio Navarro-Huerta, P.N. Nesterenko, Efthimia Papastavros, P. Peluso, Erika Pfaunmiller, Colin F. Poole, S. Della Posta, Jan Přikryl, Michele Protti, Guillermo Quintás, M. Asensio Ramon, Anurag S. Rathore, Marja-Liisa Riekkola, M.J. Ruiz-Angel, Antonio Salgado, J. Samuelsson, Roccaldo Sardella, Deepika Sarin, Oliver J. Schmitz, Andreas Seidel-Morgenstern, Jozef Šesták, Kevin Skinley, Lloyd R. Snyder, Matthew Sobansky, André M. Striegel, José Ramón Torres-Lapasió, Anna Týčová, Deyber Arley Vargas Medina, Justyna Walczak-Skierska, Susanne K. Wiedmer, Haifei Zhang, Xiwei Zheng
Publikováno v:
Liquid Chromatography ISBN: 9780323999687
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d201e7fbcf93efff9dab01b62e405e93
https://doi.org/10.1016/b978-0-323-99968-7.09991-4
https://doi.org/10.1016/b978-0-323-99968-7.09991-4
Autor:
Amparo Alfonso, Gerardo Álvarez-Rivera, Damia Barceló, Diletta Berardinelli, Paolo Berretta, Balázs Bobály, Ana M. Botana, Luis M. Botana, Grazia Bottillo, Stefania Briganti, C. Brunelli, Carlos Calderón, Emanuela Camera, Mira Čelić, Bezhan Chankvetadze, Alejandro Cifuentes, Maura D’Amato, Chiara Dal Bosco, Miren Lopez de Alda, Annagiulia Di Trana, Cristopher Domínguez-Hernández, Paola Donato, Paola Dugo, Cemil Can Eylem, Yuchen Fan, Marinella Farré, Antonia Garrido Frenich, Alessandra Gentili, Barbara Gieroba, Helen Gika, Jesús M. González-Jartín, Javier González-Sálamo, Alexandre Goyon, Kenji Hamase, M. Hanna-Brown, Kari Hartonen, Javier Hernández-Borges, Miguel Herrero, J. Hradski, Paolo Iadarola, Elena Ibáñez, Chiharu Ishii, Gabriel Jiménez-Skrzypek, Krzysztof Jóźwiak, Hiroyuki Kataoka, Engin Koçak, Reiko Koga, Radoslaw P. Kozak, Michael Lämmerhofer, F. Lestremau, Shaoping Li, Rosalía López-Ruiz, Miriam Maiellaro, Roberto Mandrioli, M.D. Marazuela, Jesús Marín-Sáez, Joanna Matys, Laura Mercolini, Bernhard Michalke, Luigi Mondello, Eva Montanari, Emirhan Nemutlu, Volker Nischwitz, Monica Ottaviani, Jevgeni Parshintsev, Paola Peluso, Sandra Perez, Mira Petrovic, Robert S Plumb, Colin F. Poole, Michele Protti, You Qin, Marja-Liisa Riekkola, Roberto Romero-González, Louise Royle, José David Sánchez-Martínez, Lorenzo Sciuto, Bárbara Socas-Rodríguez, R. Szucs, Georgios Theodoridis, Anastasio Tini, Kenichiro Todoroki, Alberto Valdés, Mercedes R. Vieytes, Simona Viglio, Ian D Wilson, Kelly Zhang, Jing Zhao
Publikováno v:
Liquid Chromatography ISBN: 9780323999694
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8f013c0fab032f66adf5a854dbc1565
https://doi.org/10.1016/b978-0-323-99969-4.09991-5
https://doi.org/10.1016/b978-0-323-99969-4.09991-5