Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Margherita De Bonis"'
Autor:
Federico Berti, Carlo Bonini, Francesco Tramutola, Paolo Lupattelli, Rocco Pandolfo, Margherita De Bonis, Maria Funicello, Lucia Chiummiento, Nadia Di Blasio
Publikováno v:
Journal of Medicinal Chemistry. 53:1451-1457
A series of new thienyl ring containing analogues of nelfinavir and saquinavir with different substitution patterns were synthesized from suitable enantiopure diols. Their inhibitory activity against wild type recombinant HIV-1 protease was evaluated
Publikováno v:
Molecular Crystals and Liquid Crystals. 481:56-72
Synthesis and mesomorphism of novel non-symmmetric mono β-aryl (octylsulfanyl)porphyrazines and their Ni(II) complexes were reported. A recently disclosed asymmetrization procedure led to mono β-bromo substituted porphyrazines, which provided acces
Autor:
Lucia Chiummiento, Rocco Pandolfo, Carlo Bonini, Paolo Lupattelli, Margherita De Bonis, Maria Funicello
Publikováno v:
Tetrahedron: Asymmetry. 17:2919-2924
Optimized conditions for the catalytic asymmetric dihydroxylation have been applied to thiophene and benzothiophene containing acrylates and crotonates to afford the corresponding diols in good overall yields and good to excellent enantiomeric excess
Autor:
Margherita De Bonis, Francesco Lelj, Mario Amati, Tommaso R. I. Cataldi, Giuliana Bianco, Sandra Belviso
Publikováno v:
Journal of the American Society for Mass Spectrometry. 24(4)
A new hexadentate, tripodal 8-hydroxyquinoline based ligand (QH3) and its gadolinium(III) tris-chelated (GdQ) complex with hemicage structure was investigated by using high resolution Fourier-transform ion cyclotron resonance mass spectrometry (FTICR
Autor:
Maria Funicello, Carlo Bonini, Margherita De Bonis, Rocco Pandolfo, Lucia Chiummiento, Paolo Lupattelli
Publikováno v:
ChemInform. 38
Autor:
Carlo Bonini, Gerardina Suanno, Margherita De Bonis, Federico Berti, Maria Funicello, Lucia Chiummiento, Paolo Lupattelli, Pietro Campaner
An efficient method has been developed for the synthesis of a versatile intermediate bearing azido, hydroxyl and ester functions, a useful precursor for peptidomimetic compounds. The two main features for this synthesis were the use of the Sharpless
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::223dde34e29391c6f7fc8a8a58c8f0f2
http://hdl.handle.net/11368/1690770
http://hdl.handle.net/11368/1690770
A stereoselective and efficient preparation of a thiophene containing intermediate 2 from ethyl 3-thienyl propenoate 4 as the core of new possible HIV protease inhibitors is described. The chiral intermediate has been successfully used for the prepar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b485f4a96fdfd7f640929e8677029642
http://hdl.handle.net/11573/1653055
http://hdl.handle.net/11573/1653055