Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Beatriz N. Brousse"'
Autor:
Pablo D. Rouge, Beatriz N. Brousse, Albertina G. Moglioni, Guillermo A. Cozzi, Angel Alvarez-Larena, Norma D´Accorso, Graciela Y. Moltrasio
Publikováno v:
ARKIVOC, Vol 2005, Iss 12, Pp 8-21 (2005)
Externí odkaz:
https://doaj.org/article/c84a892411c14bd2bcc96408a6c9cd08
Autor:
Beatriz N. Brousse, Albertina G. Moglioni, Miriam Martins Alho, Ángel Álvarez-Larena, Graciela Y. Moltrasio, Norma B. D´Accorso
Publikováno v:
ARKIVOC, Vol 2002, Iss 10, Pp 14-23 (2002)
Externí odkaz:
https://doaj.org/article/5f2086943e9142c6b2380da86133f204
Autor:
Norma D´Accorso, Graciela Y. Moltrasio, Angel Alvarez-Larena, Pablo D. Rouge, Guillermo A. Cozzi, Beatriz N. Brousse, Albertina G. Moglioni
Publikováno v:
ARKIVOC, Vol 2005, Iss 12, Pp 8-21 (2005)
Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural α,β-unsaturated and bicyclic terpenones is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy and X-ray
Publikováno v:
Tetrahedron: Asymmetry. 14:2445-2451
Optically active cyclobutyl (Z)-α,β-dehydro-α-dipeptides have been efficiently synthesized through the coupling of conveniently protected glycine or (S)-phenylalanine residues with a (Z)-dehydro-α-amino acid derivative prepared, in turn, from (
Autor:
Angel Alvarez-Larena, Albertina G. Moglioni, Graciela Y. Moltrasio, Norma D´Accorso, Miriam A. Martins Alho, Beatriz N. Brousse
Publikováno v:
ARKIVOC, Vol 2002, Iss 10, Pp 14-23 (2002)
Preparation of chiral heterocyclic compounds of the thiadiazoline types, starting from natural terpenones such as fenchone, camphor and menthone, is described. Stereochemical assignment of the compounds synthesized was performed by NMR spectroscopy a
Autor:
Graciela Y. Moltrasio, Angel Alvarez-Larena, Albertina G. Moglioni, Beatriz N. Brousse, Rosa M. Ortuño
Publikováno v:
Tetrahedron: Asymmetry. 13:451-454
The highly stereoselective conjugate addition of nitromethane to α,β-unsaturated cyclobutyl esters derived from (−)-(S)-verbenone has been executed to afford the adducts as single stereoisomers in good yields. These products furnish cyclobutyl GA
Autor:
M. A. Martins Alho, Beatriz N. Brousse, Albertina G. Moglioni, Norma D´Accorso, Graciela Y. Moltrasio
Publikováno v:
ARKIVOC, Vol 2000, Iss 4, Pp 627-640 (2000)
Scopus-Elsevier
Arkivoc 2000;2000(4 SPECISS):627-640
Biblioteca Digital (UBA-FCEN)
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
Scopus-Elsevier
Arkivoc 2000;2000(4 SPECISS):627-640
Biblioteca Digital (UBA-FCEN)
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
The synthesis of new 1,3,4-thiadiazolines derived from diaryl and aryl-cycloalkyl ketones, via the corresponding thiosemicarbazones, is described. Hand C-NMR spectra as well as mass spectrometry disclosed the structures of the precursors and heterocy
Autor:
Albertina G. Moglioni, Miriam A. Martins Alho, Cybele C. García, Elsa B. Damonte, Marla J Carlucci, Norma B. D'Accorso, Beatriz N. Brousse, Graciela Y. Moltrasio
Publikováno v:
Antiviral chemistrychemotherapy. 14(2)
The inhibitory effect of several thiosemicarbazones (TSCs), synthesized from aromatic ketones and terpenones, and their heterocyclic thiadiazoline (TDZ) derivatives, was investigated against Junin virus (JUNV), an arenavirus agent of Argentine haemor