Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Manuele Musolino"'
Publikováno v:
Frontiers in Chemistry, Vol 7 (2019)
This review focuses on the use of dialkyl carbonates (DACs) as green reagents and solvents for the synthesis of several 5- and 6-membered heterocycles including: tetrahydrofuran and furan systems, pyrrolidines, indolines, isoindolines, 1,4-dioxanes,
Externí odkaz:
https://doaj.org/article/de9c8ef2072c41309d833af824b2dda9
Autor:
Francesco Airaghi, Andrea Fiorati, Giordano Lesma, Manuele Musolino, Alessandro Sacchetti, Alessandra Silvani
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 147-154 (2013)
Aiming at restricting the conformational freedom of tryptophan-containing peptide ligands, we designed a THBC (tetrahydro-β-carboline)-DKP (diketopiperazine)-based peptidomimetic scaffold capable of arranging in an unusual α-turn conformation. The
Externí odkaz:
https://doaj.org/article/d8a4593719364517a9a670aa59667958
Publikováno v:
Catalysis Science & Technology. 11:3411-3421
Dimethyl isosorbide (DMI) is a well-known bio-based green replacement for conventional dipolar solvents such as dimethyl sulfoxide and dimethylformamide. The synthesis of DMI mainly relies on the etherification of the bio-based platform chemical isos
Autor:
Manuele Musolino, Fabio Arico
Publikováno v:
Synthesis. 51:1770-1778
A novel halogen-free synthesis of benzo-fused six-membered 1,4-heterocycles through the chemistry of dialkyl carbonates is reported. Commercially available catechol, 2-aminophenol, and 2-aminothiophenol were reacted first with ethylene carbonate in
Autor:
Matteo Zanda, Sergio Dall'Angelo, David O'Hagan, Ian N. Fleming, Manuele Musolino, Lutz Frank Schweiger
Publikováno v:
European journal of organic chemistry (Online) 2021 (2021): 1429–1439. doi:10.1002/ejoc.202001670
info:cnr-pdr/source/autori:Musolino M.; Fleming I.N.; Schweiger L.F.; O'Hagan D.; Dall'Angelo S.; Zanda M./titolo:Synthesis, Radiosynthesis, and in vitro Studies on Novel Hypoxia PET Tracers Incorporating [18F]FDR/doi:10.1002%2Fejoc.202001670/rivista:European journal of organic chemistry (Online)/anno:2021/pagina_da:1429/pagina_a:1439/intervallo_pagine:1429–1439/volume:2021
info:cnr-pdr/source/autori:Musolino M.; Fleming I.N.; Schweiger L.F.; O'Hagan D.; Dall'Angelo S.; Zanda M./titolo:Synthesis, Radiosynthesis, and in vitro Studies on Novel Hypoxia PET Tracers Incorporating [18F]FDR/doi:10.1002%2Fejoc.202001670/rivista:European journal of organic chemistry (Online)/anno:2021/pagina_da:1429/pagina_a:1439/intervallo_pagine:1429–1439/volume:2021
M.M. thanks SULSA for a PhD studentship. We gratefully acknowledge financial support from the EPSRC (grant EP/I034793/1). We report the synthesis of five radiotracers incorporating different oxyamine spacers between the hypoxia‐reactive 2‐nitroim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c0690d787ab8e9660dc3349bcce6bcf
https://hdl.handle.net/10023/25139
https://hdl.handle.net/10023/25139
Publikováno v:
Green Chemistry. 20:28-85
The worldwide urge to embrace a sustainable and bio-compatible chemistry has led industry and academia to develop of chlorine-free methodologies focused on the use of CO2 and CO2-based compounds as feedstocks, promoters and reaction media. In this sc
Publikováno v:
Pure and Applied Chemistry. 90:93-107
Cyclization of 2-(2-hydroxyethyl)phenol via DMC chemistry in acidic conditions is herein discussed for the first time. Reaction conditions have been investigated and optimized. This substrate is quite appealing as it incorporates a 2-hydroxyethyl moi
A sustainable methodology to synthesise and screen libraries of new low-environmental impact products, suitable for removing graffiti and murals from historic building, masonries and stone artworks has been developed. This approach provided a novel s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db548e2cd9cf0f6346be1e8b2d36dca5
http://hdl.handle.net/10278/3711184
http://hdl.handle.net/10278/3711184
Publikováno v:
New York: Springer, 2019
info:cnr-pdr/source/autori:Pietro Tundo, Manuele Musolino, Fabio Aricò/titolo:Replacement of Toxic Feedstocks in Chemical Synthesis/editore: /anno:2019
info:cnr-pdr/source/autori:Pietro Tundo, Manuele Musolino, Fabio Aricò/titolo:Replacement of Toxic Feedstocks in Chemical Synthesis/editore: /anno:2019
Definition of the Subject: Phosgene and phosgene-like reagents are still employed in industry in the production of aliphatic and aromatic carbamates, along with their isocyanate derivatives. Those compounds are important precursors for the synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::a0dedc49243164a887b951efc3195a97
https://publications.cnr.it/doc/403962
https://publications.cnr.it/doc/403962
Publikováno v:
Green Chemistry and Chemical Engineering
Encyclopedia of Sustainability Science and Technology ISBN: 9781493924936
Encyclopedia of Sustainability Science and Technology ISBN: 9781493924936
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e38f683e0ed5e73b81555232790f26f5
https://doi.org/10.1007/978-1-4939-9060-3_1002
https://doi.org/10.1007/978-1-4939-9060-3_1002