Zobrazeno 1 - 10
of 3 257
pro vyhledávání: '"CHIM/06"'
Publikováno v:
Canadian Journal of Chemistry. 101:326-333
Herein we describe a convenient method for the synthesis of the β-substituted Cys analogs 1a, b and trans-β-mercapto proline 1c, from their corresponding α,β-unsaturated-α-amino esters using p-methoxybenzyl mercaptan as the sulfur source. The in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::151b87a84786ed9d41c38ad70d2b7551
https://doi.org/10.1139/cjc-2022-0161
https://doi.org/10.1139/cjc-2022-0161
Publikováno v:
The Journal of Organic Chemistry. 88:5285-5290
The regioselective nitration of 9,9′-spirobifluorene under mild conditions is reported for the first time by operating under Menke’s and Crivello’s conditions. The optimized protocol allows obtaining 2-nitro and 2,2′-dinitro-9,9′-spirobiflu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d09b7bff41fd55f386962d8ca232116
https://doi.org/10.1021/acs.joc.2c02596
https://doi.org/10.1021/acs.joc.2c02596
Autor:
Paola Bambina, Alberto Spinella, Giuseppe Lo Papa, Delia Francesca Chillura Martino, Paolo Lo Meo, Onofrio Corona, Luciano Cinquanta, Pellegrino Conte
Publikováno v:
Journal of Agricultural and Food Chemistry. 71:5823-5835
In this study, the soil effect on the micro-component composition of Nero d'Avola wines obtained from different locations was investigated through 1H NMR-based metabolomics. Two different approaches were applied: the targeted (TA) and the non-targete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e56aac69cf1c7cd34b45f275c2d694d
https://doi.org/10.1021/acs.jafc.2c08654
https://doi.org/10.1021/acs.jafc.2c08654
Autor:
Daniele Del Giudice, Matteo Valentini, Carla Sappino, Emanuele Spatola, Aurora Murru, Gianfranco Ercolani, Stefano Di Stefano
Publikováno v:
The Journal of Organic Chemistry. 88:4379-4386
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::296bd45c2f7ad7732c80d5a49fbcdd16
https://doi.org/10.1021/acs.joc.2c02992
https://doi.org/10.1021/acs.joc.2c02992
Autor:
Andrea Citarella, Davide Moi, Martina Pedrini, Helena Pérez-Peña, Stefano Pieraccini, Alessandro Dimasi, Claudio Stagno, Nicola Micale, Tanja Schirmeister, Giulia Sibille, Giorgio Gribaudo, Alessandra Silvani, Clelia Giannini, Daniele Passarella
Publikováno v:
Organic & Biomolecular Chemistry. 21:3811-3824
A panel of novel cinnamic ester derivatives showed a potent inhibitory effect against SARS-CoV-2 Mpro and efficiently impaired the in vitro replication of two human coronaviruses in the low micromolar range.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26bbb8c08deeebf180f9bebf1f8c6ece
https://doi.org/10.1039/d3ob00381g
https://doi.org/10.1039/d3ob00381g
Autor:
Daniele Polidoro, Daniel Ballesteros-Plata, Alvise Perosa, Enrique Rodríguez-Castellón, Daily Rodríguez-Padrón, Maurizio Selva
Publikováno v:
Catalysis Science & Technology. 13:2223-2238
Non-noble metal nanoparticles supported on biomass-derived N-doped carbons as efficient and selective catalytic systems in alcohols oxidation reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77f546d8677bee91a063da219206a56f
https://doi.org/10.1039/d3cy00082f
https://doi.org/10.1039/d3cy00082f
Publikováno v:
Chemical Communications. 59:3281-3284
A redox umpolung strategy for the synthesis of complex tetrahydrocarbazoles is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8b704be7cf67f1a01676473a81689ff
https://doi.org/10.1039/d2cc06723d
https://doi.org/10.1039/d2cc06723d
Publikováno v:
RSC Advances. 13:9065-9077
KuQuinones: from serendipity synthesis to photo(electro)chemical and biomedical applications.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::604ad52839cc737ac74f52537888f6c2
https://doi.org/10.1039/d3ra00539a
https://doi.org/10.1039/d3ra00539a
Autor:
Longbin Liu, Peter D. Johnson, Michael E. Prime, Vinod Khetarpal, Christopher J. Brown, Luca Anzillotti, Daniele Bertoglio, Xuemei Chen, Samuel Coe, Randall Davis, Anthony P. Dickie, Simone Esposito, Elise Gadouleau, Paul R. Giles, Catherine Greenaway, James Haber, Christer Halldin, Scott Haller, Sarah Hayes, Todd Herbst, Frank Herrmann, Manuela Heßmann, Ming Min Hsai, Yaser Khani, Adrian Kotey, Angelo Lembo, John E. Mangette, Gwendolyn A. Marriner, Richard W. Marston, Matthew R. Mills, Edith Monteagudo, Anton Forsberg-Morén, Sangram Nag, Laura Orsatti, Christine Sandiego, Sabine Schaertl, Joanne Sproston, Steven Staelens, Jack Tookey, Penelope A. Turner, Andrea Vecchi, Maria Veneziano, Ignacio Muñoz-Sanjuan, Jonathan Bard, Celia Dominguez
Publikováno v:
Journal of Medicinal Chemistry. 66:641-656
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74e78d658107fd1300b7add11eee0911
https://doi.org/10.1021/acs.jmedchem.2c01585
https://doi.org/10.1021/acs.jmedchem.2c01585
Publikováno v:
Chemistry; Volume 4; Issue 4; Pages: 1624-1653
Since chlorohydrazones are planar molecules, it is in principle possible to distinguish between their E and Z stereoisomers. Chlorohydrazones are known to preferentially assume the Z configuration around the C=N double bond, and their (E, Z) isomeriz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5061eb55d8ab20bf04cf093795685131
https://doi.org/10.3390/chemistry4040106
https://doi.org/10.3390/chemistry4040106