Zobrazeno 1 - 4
of 4
pro vyhledávání: '"§ Ma Dolores García-Grávalos"'
Autor:
Arturo San Feliciano, Aurora Molinari, Pablo Chamorro, Ma Angeles Castro, José M. Miguel del Corral, and Howard B. Broughton, Ma Mar Mahiques, § Ma Dolores García-Grávalos, M. Gordaliza
Publikováno v:
Journal of Medicinal Chemistry. 44:1257-1267
A new series of diterpenylquinone/hydroquinones has been prepared by Diels-Alder cycloaddition between three labdanic diterpenoids (myrceocommunic acid, methyl myrceocommunate, and myrceocommunyl acetate) and p-benzoquinone or 1,4-naphthoquinone. Inf
Autor:
Ma Luisa López-Vázquez, Howard B. Broughton, Marina Gordaliza, § Ma Dolores García-Grávalos, Arturo San Feliciano, Ma Angeles Castro, JoséMa Miguel del Corral
Publikováno v:
Tetrahedron. 53:6555-6564
A new type of cyclolignans with an isoxazoline ring fused to the cyclolignan core has been prepared from 7-ketolignanolides by reaction with hydroxylamine. The corresponding 7-oxime derivatives have also been obtained. The compounds prepared have bee
Autor:
Alfonso Oliva, José M. Miguel del Corral, Marina Gordaliza, Nanet Aguilera, Aurora Molinari, § Ma Dolores García-Grávalos, Ma Angeles Castro, Arturo San Feliciano
Publikováno v:
Boletín de la Sociedad Chilena de Química v.46 n.1 2001
SciELO Chile
CONICYT Chile
instacron:CONICYT
Boletín de la Sociedad Chilena de Química, Volume: 46, Issue: 1, Pages: 33-39, Published: MAR 2001
SciELO Chile
CONICYT Chile
instacron:CONICYT
Boletín de la Sociedad Chilena de Química, Volume: 46, Issue: 1, Pages: 33-39, Published: MAR 2001
Several new 2,3-functionally dialkyl-1,4-benzohydroquinone diacetates have been prepared by oxidative cleavage of epoxide compounds III, obtained from the Diels-Alder condensation product between the monoterpene myrcene and 1,4-benzoquinone. The natu
Autor:
José M. Miguel del Corral, § Ma Dolores García-Grávalos, Nanet Aguilera, Aurora Molinari, Ma Angeles Castro, Alfonso Oliva, Arturo San Feliciano, Marina Gordaliza
Publikováno v:
Bioorganicmedicinal chemistry. 8(5)
Several prenylhydroquinones have been prepared through Diels-Alder condensation, further functionalized or degraded chemically and then evaluated for their cytotoxic activity against some neoplastic cultured cell lines. A number of them have shown IC