Zobrazeno 1 - 10
of 167
pro vyhledávání: '"Paolo Venturello"'
Publikováno v:
Molecules, Vol 18, Iss 1, Pp 1188-1213 (2013)
Since the first report and due to its handiness and wide scope, the Suzuki-Miyaura (SM) cross coupling reaction has become a routine methodology in many laboratories worldwide. With respect to other common transition metal catalyzed cross couplings,
Externí odkaz:
https://doaj.org/article/d2ea955394344bebadbe6237429cbe58
Publikováno v:
Molecules, Vol 15, Iss 4, Pp 2667-2685 (2010)
This review is an overview of the last ten years’ use of the Mizoroki–Heck coupling applied to 1,2- and 1,3-dienes. Since both these systems form π-allyl palladium intermediates in Pd(0) coupling, they show particular chemical behavior. Many exa
Externí odkaz:
https://doaj.org/article/ba655084fc52434fa56ec95f217952c9
Autor:
Silvano Cadamuro, Paolo Venturello, Giulia Spano, Marta Rucci, Margherita Barbero, Stefano Dughera
Publikováno v:
Tetrahedron. 70:1818-1826
A simple and efficient alkylation of aromatic and heteroaromatic compounds via the direct S N 1-type nucleophilic substitution of benzylic alcohols in the presence of catalytic amounts of the strong Bronsted acid o -benzenedisulfonimide under neat co
Autor:
Paolo Arru, Niccolo Bianco, Annamaria Deagostino, Cristina Prandi, Antonio Toppino, Paolo Venturello
Publikováno v:
European Journal of Organic Chemistry. 2013:6990-6997
A Mizoroki–Heck–heteroannulation cascade reaction has been used to prepare substituted dihydrobenzofurans and indolines in good yields by the reaction between functionalised alkoxy-1,3-dienes and several o-iodophenols or protected o-iodoanilines.
Publikováno v:
Molecules
Molecules, Vol 18, Iss 1, Pp 1188-1213 (2013)
Molecules, Vol 18, Iss 1, Pp 1188-1213 (2013)
Since the first report and due to its handiness and wide scope, the Suzuki-Miyaura (SM) cross coupling reaction has become a routine methodology in many laboratories worldwide. With respect to other common transition metal catalyzed cross couplings,
Publikováno v:
ChemInform. 47
The reactivity of metalated alkoxy-1,3-dienes and α-aryl-N-phenylnitrones in the presence of LIC-KOR base, equimolar mixture of alkyllithium (LIC) and potassium alcoxides (KOR), (Schlosser, 1994) [1] has been studied. A cascade reaction involving a
Publikováno v:
Synthesis. 44:3688-3692
The enantiodivergent synthesis of the Streptomyces alkaloid 4- epi -SS20846A was based on a Takai olefination/Suzuki–Miyaura coupling sequence for the highly stereoselective introduction of the E , E -pentadienyl side chain on the piperidine skel
Publikováno v:
ResearcherID
Autor:
Eleonora Mussano, Cristina Prandi, Gianluca Croce, Paolo Venturello, Marco Blangetti, Annamaria Deagostino
Publikováno v:
The Journal of Organic Chemistry. 76:1814-1820
The direct addition of metalated alkoxydiene 2, obtained from α,β-unsaturated acetal 1 through a LIC-KOR-promoted conjugated elimination reaction, to enantiopure sulfinimines 3 (both R and SN-sulfinyl imines) afforded N-sulfinyl alkoxydienyl amines
Autor:
Silvano Cadamuro, Stefano Dughera, Claudio Magistris, Paolo Venturello, Stefano Bazzi, Margherita Barbero
Publikováno v:
Synlett. 2010:1803-1806
Arene mono- and disulfonyl chlorides have been easily synthesized starting from the corresponding anilines via aqueous oxidative chlorination of S-aryl O-ethyl dithiocarbonates intermediates, aryl methyl sulfides, or from arenethiols.