Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Mattia Moiola"'
Publikováno v:
ChemistryOpen, Vol 9, Iss 2, Pp 195-199 (2020)
Abstract 1,2,4‐Oxadiazole[4,5‐a]piridinium salts add alcohols and alkoxides to undergo electrocyclic ring opening affording alkoxybutadienyl 1,2,4‐oxadiazole derivatives. The pyridinium salts represent a special class of Zincke salts that are p
Externí odkaz:
https://doaj.org/article/24d1557a23c847538f3ef6fae14108c0
Autor:
Dr. Mattia Moiola, Dr. Antonio Bova, Dr. Stefano Crespi, Dr. Misal G. Memeo, Prof. Mariella Mella, Prof. Herman S. Overkleeft, Dr. Bogdan I. Florea, Prof. Paolo Quadrelli
Publikováno v:
ChemistryOpen, Vol 8, Iss 6, Pp 770-780 (2019)
Abstract Anthracenenitrile oxide undergoes 1,3‐dipolar cycloaddition reaction with propargyl bromide affording the expected isoxazole as single regioisomer, suitably synthetically elaborated and functionalized with a protected triple bond. The intr
Externí odkaz:
https://doaj.org/article/eaae9e8dc30346c3ad3d98857a076d77
Autor:
Mattia Moiola, Stefano Crespi, Misal Memeo, Simona Collina, Herman Overkleeft, Bogdan Florea, Paolo Quadrelli
Publikováno v:
ACS Omega, Vol 4, Iss 4, Pp 7766-7774 (2019)
Externí odkaz:
https://doaj.org/article/22860778d8c74f9eb677c561775ba10e
Autor:
Misal Giuseppe Memeo, Elena Valletta, Beatrice Macchi, Alessio Porta, Bruna Bovio, Mattia Moiola, Paolo Quadrelli
Publikováno v:
ACS Omega, Vol 3, Iss 7, Pp 7621-7629 (2018)
Externí odkaz:
https://doaj.org/article/22b1d91c233241c8b7087c95bceeec79
Publikováno v:
Molecules, Vol 24, Iss 20, p 3654 (2019)
Peptide-based drugs, despite being relegated as niche pharmaceuticals for years, are now capturing more and more attention from the scientific community. The main problem for these kinds of pharmacological compounds was the low degree of cellular upt
Externí odkaz:
https://doaj.org/article/8dd942609b1c4aa6afc8c329b20ffed9
Publikováno v:
Synthesis. 53:574-586
The generation and trapping of two new nitrosocarbonyl intermediates bearing carbohydrate-based chiral substituents is achieved by the mild oxidation of the corresponding nitrile oxides with tertiary amine N-oxides. Their capture with suitable dienes
Publikováno v:
ChemistrySelect. 5:5367-5373
Publikováno v:
ChemistryOpen
ChemistryOpen, Vol 9, Iss 2, Pp 195-199 (2020)
ChemistryOpen, Vol 9, Iss 2, Pp 195-199 (2020)
1,2,4‐Oxadiazole[4,5‐a]piridinium salts add alcohols and alkoxides to undergo electrocyclic ring opening affording alkoxybutadienyl 1,2,4‐oxadiazole derivatives. The pyridinium salts represent a special class of Zincke salts that are prone to r
Autor:
Bogdan I. Florea, Misal Giuseppe Memeo, Herman S. Overkleeft, Paolo Quadrelli, Mattia Moiola, Mariella Mella, Stefano Crespi, Antonio Bova
Publikováno v:
ChemistryOpen, Vol 8, Iss 6, Pp 770-780 (2019)
ChemistryOpen, 8(6), 770-780
ChemistryOpen
ChemistryOpen, 8(6), 770-780
ChemistryOpen
Anthracenenitrile oxide undergoes 1,3‐dipolar cycloaddition reaction with propargyl bromide affording the expected isoxazole as single regioisomer, suitably synthetically elaborated and functionalized with a protected triple bond. The introduction
Autor:
Paolo Quadrelli, Mattia Moiola, Misal Giuseppe Memeo, Faiq Hamasaid Hussain, Karzan Khaleel Hameed, Ahmed Anwar Amin
Publikováno v:
Synthesis. 51:1383-1390
An easy approach to N-hydroxy-N-cycloalkenylamides, ene adducts of cyclic alkenes of different sizes, is presented. The products can be obtained both through the thermal generation of the nitrosocarbonyl intermediates and via the photochemical fragme