Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Claudio Monasterolo"'
Autor:
Claudio Monasterolo, Mauro F. A. Adamo
Publikováno v:
Organic Letters. 24:4729-4733
The first example of an aromatic haloform reaction is reported, defining a conceptually new haloform-type approach to the metal-free functionalization of arenes. We demonstrated that heteroarenes bearing a vinylogous nitromethane system, via the stag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03ee58e08fc969709e4d10d605e293e4
https://doi.org/10.1021/acs.orglett.2c01494
https://doi.org/10.1021/acs.orglett.2c01494
Autor:
Brian G. Kelly, Martina Costanzo, Mauro Cortigiani, Claudio Monasterolo, Malachi W. Gillick-Healy, Mauro F. A. Adamo
Publikováno v:
European Journal of Organic Chemistry. 2021:4560-4565
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edfdd5f6afa5f45703dcfe4c106eea5c
https://doi.org/10.1002/ejoc.202100502
https://doi.org/10.1002/ejoc.202100502
Autor:
Claudio Monasterolo, Ryan O'Gara, Saranna E. Kavanagh, Sadbh E. Byrne, Bartosz Bieszczad, Orla Murray, Michael Wiesinger, Rebecca A. Lynch, Kirill Nikitin, Declan G. Gilheany
Publikováno v:
Chemical science. 13(21)
A new class of biaryl chiral ligands derived from 1,2-diaminocyclohexane (1,2-DACH) has been designed to enable the asymmetric addition of aliphatic and, for the first time, aromatic Grignard reagents to ketones for the preparation of highly enantioe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17d56c1f3fbe2cf6b2b9df72fe514084
https://pubmed.ncbi.nlm.nih.gov/35733895
https://pubmed.ncbi.nlm.nih.gov/35733895
Publikováno v:
Chemical Science. 10:6531-6538
Phenones with elongated chains are shown to be excellent substrates for ligand-promoted asymmetric Grignard synthesis of tertiary alcohols. In turn this enables the simple, short and highly enantioselective (up to 96% ee) preparation of chiral 2,2-di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55fa4676fad4d89526c1f3c3aa489996
https://doi.org/10.1039/c9sc00978g
https://doi.org/10.1039/c9sc00978g
Autor:
Martina Costanzo, Claudio Monasterolo, Brian G. Kelly, Mauro Cortigiani, Mauro F. A. Adamo, Malachi W. Gillick-Healy
Publikováno v:
European Journal of Organic Chemistry. 2021:4559-4559
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54a2e01f244181de4271d353eaf6d6ea
https://doi.org/10.1002/ejoc.202100933
https://doi.org/10.1002/ejoc.202100933
Publikováno v:
Tetrahedron Letters. 58:4205-4208
Herein we describe the preparation of a new class of sterically demanding organocatalysts derived from d -fructose and their use, alongside hitherto unreported doubly quaternarised Cinchona ammonium salts, in the Michael reaction of nitromethane with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb312d50e1e544c6644753fbcb80312e
https://doi.org/10.1016/j.tetlet.2017.09.067
https://doi.org/10.1016/j.tetlet.2017.09.067
Publikováno v:
Tetrahedron Letters. 56:7168-7171
Herein, we report our investigation into the reactivity of 5-enamino-4-nitroisoxazoles. This study revealed that the title compounds, in spite of conjugation to the 4-nitroisoxazole, displayed similar reactivity to enamines, reacting with electrophil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::578d7f11329afda76d0a272b4818951c
https://doi.org/10.1016/j.tetlet.2015.11.037
https://doi.org/10.1016/j.tetlet.2015.11.037
Autor:
Pedro Blas González, Mauro Comes Franchini, Lorenzo Caruana, Mariafrancesca Fochi, Jay Zumbar Chandanshive, Luca Bernardi, Andrea Mazzanti, Erica Locatelli, Claudio Monasterolo, Bianca F. Bonini
Publikováno v:
European Journal of Organic Chemistry. 2013:8108-8114
The reactivity of the ynamide tert-butyl N-ethynyl-N-phenylcarbamate (1) in the 1,3-dipolar cycloaddition (1,3-DC) with C-carboxymethyl-N-phenylnitrilimine was investigated. This [3+2] cycloaddition affords the 5-amino pyrazole as a single regioisome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cdeb376cdd22fee37a92584bb78b3aa
https://doi.org/10.1002/ejoc.201301054
https://doi.org/10.1002/ejoc.201301054
ChemInform Abstract: Preparation and Reactivity of [2-(3-Methyl-4-nitro-isoxazol-5-yl)-vinyl]-amines
Publikováno v:
ChemInform. 47
Herein, we report our investigation into the reactivity of 5-enamino-4-nitroisoxazoles. This study revealed that the title compounds, in spite of conjugation to the 4-nitroisoxazole, displayed similar reactivity to enamines, reacting with electrophil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4d59be0b50429895012df333754b1af
https://doi.org/10.1002/chin.201621173
https://doi.org/10.1002/chin.201621173
Autor:
Anna Rita Bilia, Maria Camilla Bergonzi, Claudio Monasterolo, Maria Cristina Falconieri, Marcella Coronnello, Mauro F. A. Adamo
Publikováno v:
Planta medica. 83(5)
Curcumin, the main curcuminoid of the popular Indian spice turmeric, is a potent chemopreventive agent and useful in many different diseases. A major limitation of applicability of curcumin as a health promoting and medicinal agent is its extremely l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::649a3f9ccb8b03ffe162c68aa3c1d651
https://pubmed.ncbi.nlm.nih.gov/27002394
https://pubmed.ncbi.nlm.nih.gov/27002394