Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Alberto Oppedisano"'
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-7 (2017)
Alkenes are versatile buildings blocks in organic synthesis. Here, the authors developed a three-membered ring strategy to access a variety of functionalized alkenes by coupling of in-situ generated azines with sulfoxonium ylides.
Externí odkaz:
https://doaj.org/article/8f17816b542a465ca9b3389209a9c74a
Autor:
Rafael Gomes, Thomas Alexander Stephens, Iakovos Saridakis, Nuno Maulide, Rik Oost, Christian Knittl-Frank, Alberto Oppedisano, Antonio Misale, James D. Neuhaus
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
The metal‐promoted nucleophilic addition of sulfur ylides to π‐systems is a well‐established reactivity. However, the driving force of such transformations, elimination of a sulfide moiety, entails stoichiometric byproducts making them unfavor
Autor:
Alberto Oppedisano, Veronica Tona, Saad Shaaban, Daniel Kaiser, Carlos R. Gonçalves, Nuno Maulide
Publikováno v:
Angewandte Chemie. 131:14781-14785
Autor:
Stefano Nejrotti, Andrea Maranzana, Annamaria Deagostino, Cristina Prandi, Gabriele Prina Cerai, Ernesto G. Occhiato, Dina Scarpi, Alberto Oppedisano
Publikováno v:
European Journal of Organic Chemistry. 2017:6228-6238
The gold-catalyzed oxidation of N-tosyl-protected 6-alkynyl-3,4-dihydro-2H-pyridines was studied in detail to obtain divinyl ketones in which one of the double bond is embedded in a heterocyclic framework. The best reaction conditions were then exten
Autor:
James D. Neuhaus, Rik Oost, Alberto Oppedisano, Christian Knittl-Frank, Iakovos Saridakis, Antonio Misale, Thomas Alexander Stephens, Nuno Maulide, Rafael Gomes
Publikováno v:
Chemistry – A European Journal. 26:10905-10905
Autor:
Ernesto G. Occhiato, Cristina Prandi, Annamaria Deagostino, Enrique Gómez-Bengoa, Stefano Begliomini, Alberto Oppedisano, Dina Scarpi, Béla Fiser
Publikováno v:
European Journal of Organic Chemistry. 2015:3251-3265
The gold(I)-catalysed reaction of N-Boc-protected 6-alkynyl-3,4-dihydro-2H-pyridines, which gives synthetically useful vinylogous amides (β-enaminones), has been studied in detail, in order to optimize the reaction conditions, enlarge the scope and
Publikováno v:
Nature Communications
Nature Communications, Vol 8, Iss 1, Pp 1-7 (2017)
Nature Communications, Vol 8, Iss 1, Pp 1-7 (2017)
The carbon–carbon double bond, with its diverse and multifaceted reactivity, occupies a prominent position in organic synthesis. Although a variety of simple alkenes are readily available, the mild and chemoselective introduction of a unit of unsat
Publikováno v:
Journal of the American Chemical Society
Few methods permit the hydrogenation of alkenes to a thermodynamically favored configuration when steric effects dictate the alternative trajectory of hydrogen delivery. Dissolving metal reduction achieves this control, but with extremely low functio
Autor:
Nicoletta Protti, Alberto Oppedisano, Emanuele Azzi, Annamaria Deagostino, Stefano Parisotto, Saverio Altieri, Diego Alberti, Simonetta Geninatti-Crich
Publikováno v:
Bioorganic Chemistry. 93:103324
Curcumin is currently being investigated for its capacity to treat many types of cancer and to prevent the neuron damage that is observed in Alzheimer’s disease (AD). However, its clinical use is limited by its low stability and solubility in aqueo
Autor:
Silvia Tabasso, Ernesto G. Occhiato, Helena Rosso, Gabriele Alberto, Marco Blangetti, Cristina Prandi, Alberto Oppedisano, Beatrice Lace
Publikováno v:
Molecular Plant. 6:113-127
Originally identified as allelochemicals involved in plant-parasite interactions, more recently, Strigolactones (SLs) have been shown to play multiple key roles in the rhizosphere communication between plants and mycorrhizal fungi. Even more recent i