Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Maria Ciaccia"'
Autor:
Ian Priestley, Claudio Battilocchio, Andrei V. Iosub, Fabien Barreteau, Gavin W. Bluck, Kenneth B. Ling, Katharine Ingram, Maria Ciaccia, Jamie A. Leitch, Duncan L. Browne
Publikováno v:
Organic Process Research & Development. 27:269-275
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b489b56fe9097f08c4688c0b9890d2c5
https://doi.org/10.1021/acs.oprd.2c00226
https://doi.org/10.1021/acs.oprd.2c00226
Publikováno v:
Journal of the American Chemical Society. 141:10862-10875
Covalent templating provides an attractive solution to the controlled synthesis of linear oligomers because a template oligomer can be used to define the precise length and sequence of the product. If the monomer units are attached to the template us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::471676c3978d24d5de5aa7107eaca919
https://doi.org/10.1021/jacs.9b04973
https://doi.org/10.1021/jacs.9b04973
Publikováno v:
RSC Advances. 9:29566-29569
Covalent template-directed synthesis was used to oligomerise monomer building blocks in a controlled manner to give exclusively the linear trimer. Competing reaction pathways were blocked by addition of a large excess of a monomeric capping agent. At
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::154460d1e19a47fc51ebd83cfc0645f2
https://doi.org/10.1039/c9ra07233k
https://doi.org/10.1039/c9ra07233k
Publikováno v:
Chemical Science. 10:5258-5266
Template-directed synthesis is the biological method for the assembly of oligomers of defined sequence, providing the molecular basis for replication and the process of evolution. To apply analogous processes to synthetic oligomeric molecules, method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a357b522c7324377a41e691fa52a67f8
https://doi.org/10.1039/c9sc01460h
https://doi.org/10.1039/c9sc01460h
Publikováno v:
RSC advances. 9(51)
Covalent template-directed synthesis was used to oligomerise monomer building blocks in a controlled manner to give exclusively the linear trimer. Competing reaction pathways were blocked by addition of a large excess of a monomeric capping agent. At
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db37da6db4ce02b43c2c6b3a11d01211
https://pubmed.ncbi.nlm.nih.gov/35531529
https://pubmed.ncbi.nlm.nih.gov/35531529
Autor:
Matthew J. Langton, Christopher A. Hunter, Nicholas H. Williams, Maria Ciaccia, Flore Keymeulen
Publikováno v:
Nature Chemistry. 9:426-430
Transmission and amplification of chemical signals across lipid bilayer membranes is of profound significance in many biological processes, from the development of multicellular organisms to information processing in the nervous system. In biology, m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7654a83b594a7ecf41f6c2c4aa55e785
https://doi.org/10.1038/nchem.2678
https://doi.org/10.1038/nchem.2678
Autor:
Roberta Cacciapaglia, Irene Tosi, Maria Ciaccia, Luigi Mandolini, Stefano Di Stefano, Christopher A. Hunter, Laura Baldini
Publikováno v:
Chemical science (Camb. 2010. Online) 6 (2015): 144–151. doi:10.1039/c4sc02347a
info:cnr-pdr/source/autori:Ciaccia M., Tosi I., Baldini L., Cacciapaglia R., Mandolini L., Di Stefano S., Hunter C. A./titolo:Applications of dynamic combinatorial chemistry for the determination of effective molarity/doi:10.1039%2Fc4sc02347a/rivista:Chemical science (Camb. 2010. Online)/anno:2015/pagina_da:144/pagina_a:151/intervallo_pagine:144–151/volume:6
Chemical Science
info:cnr-pdr/source/autori:Ciaccia M., Tosi I., Baldini L., Cacciapaglia R., Mandolini L., Di Stefano S., Hunter C. A./titolo:Applications of dynamic combinatorial chemistry for the determination of effective molarity/doi:10.1039%2Fc4sc02347a/rivista:Chemical science (Camb. 2010. Online)/anno:2015/pagina_da:144/pagina_a:151/intervallo_pagine:144–151/volume:6
Chemical Science
Chain-stoppers give rise to ring-chain equilibria in dynamic libraries allowing determination of thermodynamic effective molarities for macrocylisation reactions.
A new strategy for determining thermodynamic effective molarities (EM) for macrocy
A new strategy for determining thermodynamic effective molarities (EM) for macrocy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44e09e4f76d9ad70fa8d1a72b6cc9ca5
https://doi.org/10.1039/c4sc02347a
https://doi.org/10.1039/c4sc02347a
Autor:
Michael J.O. Wakelam, Jane A. McKeating, Thomas F. Baumert, Simon A. Rudge, Maria Ciaccia, Laurent Mailly, Ke Hu, Margaret Ashcroft, Isla S. Humphreys, Stephanie Roessler, Bishnupriya Bhattacharya, Qifeng Zhang, Garrick K. Wilson, Michelle J. Farquhar, Gary M. Reynolds, Peter Balfe
Publikováno v:
Journal of Hepatology
Journal of Hepatology, Elsevier, 2017, 66 (5), pp.919-929. ⟨10.1016/j.jhep.2017.01.009⟩
Journal of Hepatology, Elsevier, 2017, 66 (5), pp.919-929. ⟨10.1016/j.jhep.2017.01.009⟩
BACKGROUND AND AIMS: Chronic hepatitis C is a global health problem with an estimated 170 million HCV infected individuals at risk of progressive liver disease and hepatocellular carcinoma (HCC). Autotaxin (ATX) is a phospholipase with diverse roles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::395813d374cd959633d92d58ff2fc329
https://pubmed.ncbi.nlm.nih.gov/28126468
https://pubmed.ncbi.nlm.nih.gov/28126468
Autor:
Stefano Di Stefano, Maria Ciaccia
Publikováno v:
ChemInform. 46
The state of the art in the mechanisms operating in imine chemistry in organic solvents is critically discussed in the present review. In particular, the reaction pathways involved in imine formation, transimination and imine metathesis in organic me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ad33dabde069440d156476184972e07
https://doi.org/10.1002/chin.201511324
https://doi.org/10.1002/chin.201511324
Autor:
Stefano Di Stefano, Maria Ciaccia
Publikováno v:
Organic & biomolecular chemistry 13 (2015): 646–654. doi:10.1039/c4ob02110j
info:cnr-pdr/source/autori:M: Ciaccia, S. Di Stefano/titolo:Mechanisms of imine exchange reactions in organic solvents/doi:10.1039%2Fc4ob02110j/rivista:Organic & biomolecular chemistry/anno:2015/pagina_da:646/pagina_a:654/intervallo_pagine:646–654/volume:13
info:cnr-pdr/source/autori:M: Ciaccia, S. Di Stefano/titolo:Mechanisms of imine exchange reactions in organic solvents/doi:10.1039%2Fc4ob02110j/rivista:Organic & biomolecular chemistry/anno:2015/pagina_da:646/pagina_a:654/intervallo_pagine:646–654/volume:13
The state of the art in the mechanisms operating in imine chemistry in organic solvents is critically discussed in the present review. In particular, the reaction pathways involved in imine formation, transimination and imine metathesis in organic me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6cb0c94d6027c6d716db642e82c08db
