Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Panzalorto"'
Publikováno v:
In Inorganica Chimica Acta 2 September 1999 292(1):84-95
Publikováno v:
In Thermochimica Acta 1999 329(1):39-46
Publikováno v:
Inorganica Chimica Acta. 292:84-95
The bis-4-phosphinito ligands [( p -Ph 2 POC 6 H 4 ) 2 X] (X=O, 1 ; X=CMe 2 , 2 ; X=S, 3 ) react with [Ru(η 6 - p -cymene)Cl 2 ] 2 to form the binuclear complexes {[Ru(η 6 - p -cymene)Cl 2 ] 2 [μ-( p -Ph 2 POC 6 H 4 ) 2 X]} (X=O, 4 ; X=CMe 2 , 5 ;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a4975fc8d750cec6d9fe4ec52ceab60
https://doi.org/10.1016/s0020-1693(99)00174-7
https://doi.org/10.1016/s0020-1693(99)00174-7
Publikováno v:
Scopus-Elsevier
Gold on iron oxides catalysts have been characterized by temperature programmed reduction (TPR) and X-ray diffraction spectroscopy (XRD). The influence of preparation method, gold loading and pretreatment conditions on the reducibility of iron oxides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::610000a1ad7edf87c31ab9e10f31b7e8
https://doi.org/10.1016/s0040-6031(98)00664-9
https://doi.org/10.1016/s0040-6031(98)00664-9
Publikováno v:
Inorganica Chimica Acta. 277:119-126
The chiral diphenylphosphinoxy P,N-ligands (+)-(2S,3R)-4-dimethylamino-3-methyl-1,2-diphenyl-2-diphenylphophinoxybutane (2) and (+)-(1S,2R)-2-dimethyl-amino-1-phenyl-1-diphenylphosphinoxy-propane (3) have been prepared starting from the corresponding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::836238d279254852f0030b821e60c358
https://doi.org/10.1016/s0020-1693(97)06085-4
https://doi.org/10.1016/s0020-1693(97)06085-4
Autor:
Placido Giannetto, Giuseppe Bruno, Anna Barattucci, Manuela Panzalorto, Maria C. Aversa, Paola Bonaccorsi
Publikováno v:
Tetrahedron: Asymmetry. 8:2989-2995
LiClO 4 catalyzed cycloaddition of (R S ,E)-3-[(1S)-isoborneol-10-sulfinyl]-1-methoxybuta-1,3-diene 1 with ethyl glyoxalate occurred with good endo and facial diastereoselectivities to give (2R,6S,R S )-6-ethoxycarbonyl-4-[(1S)-isoborneol-10-sulfinyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::303f185d9ee16ea500d333146757a136
https://doi.org/10.1016/s0957-4166(97)00345-5
https://doi.org/10.1016/s0957-4166(97)00345-5
Autor:
Anna Barattucci, Placido Giannetto, Paola Bonaccorsi, Manuela Panzalorto, Simona Rizzo, Maria C. Aversa
Publikováno v:
ChemInform. 29
Uncatalyzed cycloadditions of (RS,E)-1 and (RS,Z)-3-[(1S)-isoborneol-10-sulfinyl]-1-methoxybuta-1,3-diene 2 with maleimide and N-phenylmaleimide occurred with complete endo and very high facial diastereoselectivities. The effects of Lewis acid cataly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f46537a19acef9fd4d012f3008460d4a
https://doi.org/10.1002/chin.199838048
https://doi.org/10.1002/chin.199838048
Autor:
Giuseppe Bruno, G. Saitta, Manuela Panzalorto, Alessia Arena, Salvatore Patanè, Rosario Scopelliti
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 54:2003-2005
The title compound, C12H6N4, may be considered as the hydrogenated form of tetracyanoquinodimethane. The main property shown in the solid state is determined by the luminescence (blue-green emission) and it is due to the stacking interaction establ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fecd79c9bc2fda7e6f422a611138d63c
https://doi.org/10.1107/s0108270198009500
https://doi.org/10.1107/s0108270198009500
Autor:
Ambra, De Gregorio, Roberto, Battistutta, Nicoletta, Arena, Manuela, Panzalorto, Pietro, Francescato, Giovanna, Valentini, Giuseppe, Bruno, Giuseppe, Zanotti
Publikováno v:
Organicbiomolecular chemistry. 1(18)
Ornithine transcarbamoylase from ovine liver has been purified to homogeneity. Like all anabolic OTCs, the ovine enzyme is a trimer, constituted by identical subunits of 34 kDa. Sequence analysis of the 54 N-terminal residues of ovine OTC shows a hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::58246bef1a7aa1211d135f890a63bb97
https://pubmed.ncbi.nlm.nih.gov/14527149
https://pubmed.ncbi.nlm.nih.gov/14527149
