Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Alberto Guaragna"'
Autor:
Hans Peter Schnebli, Gino Amiconi, Alberto Guaragna, Martino Bolognesi, Patrizia Aducci, Enea Menegatti, Paolo Ascenzi, Alessandro Ballio
Publikováno v:
Journal of Molecular Recognition. 4:113-119
The binding of the recombinant proteinase inhibitor eglin c from the leech Hirudo medicinalis to serine (pro)enzymes belonging to the chymotrypsin and subtilisin families has been investigated from the thermodynamic viewpoint, between pH 4.5 and 9.5
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2369-2375
The condensation of lithium bis-p-tolylthiomethanide with protected ethyl-L-lactates gave a series of 3-alkoxy-(or 3-hydroxy-) 1, 1-bis-p-tolylthiobutan-2-ones, which were stereoselectively reduced to the corresponding syn- or anti-alcohols with dias
Publikováno v:
Tetrahedron. 44:3685-3692
4-Vinyl-substituted oxamazins 15,16, and 3 have been prepared. Key steps of the synthesis are: the preparation of protected α-amino-β-hydroxyacid 6 through ester enolate condensation of ethyl glycinate STABASE adduct 8 with CH-protected propiolalde
Publikováno v:
J. Chem. Soc., Chem. Commun.. :138-140
Several 3-substituted 2-hydroxy-1,1-bis-p-tolylthiopropanes, which are precursors of protected α-hydroxy-aldehydes, have been readily prepared in high optical purity via acylation of lithium bis-p-tolylthiomethanide and subsequent baker's yeast redu
Publikováno v:
ChemInform. 19
4-Vinyl-substituted oxamazins 15,16, and 3 have been prepared. Key steps of the synthesis are: the preparation of protected α-amino-β-hydroxyacid 6 through ester enolate condensation of ethyl glycinate STABASE adduct 8 with CH-protected propiolalde
Publikováno v:
ChemInform. 19
The condensation of lithium bis-p-tolylthiomethanide with protected ethyl-L-lactates gave a series of 3-alkoxy-(or 3-hydroxy-) 1, 1-bis-p-tolylthiobutan-2-ones, which were stereoselectively reduced to the corresponding syn- or anti-alcohols with dias
Publikováno v:
Chemischer Informationsdienst. 17
Several 3-substituted 2-hydroxy-1,1-bis-p-tolylthiopropanes, which are precursors of protected α-hydroxy-aldehydes, have been readily prepared in high optical purity via acylation of lithium bis-p-tolylthiomethanide and subsequent baker's yeast redu