Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Maria Luisa Marino"'
Publikováno v:
Neurophysiologie Clinique. 50:72-73
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01a6636d38f1216cc9922b63fa7e7e80
https://doi.org/10.1016/j.neucli.2020.01.002
https://doi.org/10.1016/j.neucli.2020.01.002
Autor:
Umberto Volpe, Maria Luisa Marino, Luca Autiero, Diana Facchini, Armida Mucci, Silvana Galderisi, Carlo Gianoglio
Objective: Previous studies have proposed music therapy (MT) as a useful rehabilitation approach for patients with psychosis, but few studies have focused on acute settings. The aim of the study was to evaluate the effects of a structured MT program
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68342fca782ae2a05aee694f15c0f5f3
http://hdl.handle.net/11591/401942
http://hdl.handle.net/11591/401942
Publikováno v:
Phytochemistry. 38:527-530
From the aerial parts of Sideritis syriaca a new flavone glycoside, 5,8,3′-trihydroxy-4′-methoxyflavone 7-(6‴- O -acetylsophoroside) was identified together with apigenin 7-(6″- p -coumaroylglucoside) and apigenin 7-(4″- p -coumaroylglucosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbac053ff99b6d0f45f6567ddf298835
https://doi.org/10.1016/0031-9422(94)00634-6
https://doi.org/10.1016/0031-9422(94)00634-6
Publikováno v:
Giornale botanico italiano. 122:291-294
Carnosol (11,12-dihydroxyabieta-8,11,13-trien-20-oic acid 20,7-lactone), and rosmanol (7α, 11, 12-trihydroxy-abieta-8, 11, 13-trien-20 oic acid-20, 6-lactone), two abietane diterpenes previously isolated from Rosmarinus officinalis, have been isolat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75ef39cb7eaad246b62b12b36c04e4dc
https://doi.org/10.1080/11263508809429410
https://doi.org/10.1080/11263508809429410
Autor:
Orietta Servettaz, Aurora Bellino, Maria Luisa Marino, Pietro Venturella, Giuseppe Venturella
Publikováno v:
Phytochemistry. 25:1195-1199
A new khellactone, bocconin, in addition to known compounds, have been isolated from Seseli bocconi subsp. bocconi and subsp. praecox Gamisans . Their structures were elucidated on the basis of spectral analyses and hydrolytic studies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb48aae6040a3f0715e989d26d87a728
https://doi.org/10.1016/s0031-9422(00)81579-4
https://doi.org/10.1016/s0031-9422(00)81579-4
Publikováno v:
Journal of Heterocyclic Chemistry. 11:603-606
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8caf0f4a965b1b04d80eb896ef46b44a
https://doi.org/10.1002/jhet.5570110427
https://doi.org/10.1002/jhet.5570110427
Publikováno v:
Synthetic Communications. 5:207-211
It is well known that 1, 4-diarylphthalazines are prepared by condensation of the appropriate ortho-diaroylbenzenes with hydrazine hydrate.1 As ortho-diaroylbenzenes can be obtained by oxidation of ortho-dibenzylbenzenes, a rapid method is proposed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a9f2d406c1b9423214b4ff5435bc005
https://doi.org/10.1080/00397917508064111
https://doi.org/10.1080/00397917508064111
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :759-762
The secondary hydroxy-group of sideridiol [(–)-kaur-15-ene-7β,19-diol](I) has been confirmed as being in the 7- rather than the 12-position. Bromination of methyl (–)-7-oxokauran-19-oate (IXb) gives methyl (–)-6β-bromo-7-oxokauran-19-oate (Xb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6397c42b5d7b508ed8256ac825380930
https://doi.org/10.1039/p19720000759
https://doi.org/10.1039/p19720000759
Publikováno v:
Tetrahedron. 29:3159-3164
The reactivity of indole derivatives towards nitrilimines has been studied. Substituents at positions 1, 2 and 3 of the indole ring greatly affect the course of the reaction. 1,3-Dipolar cycloaddition products (3a,8a,dihydropyrazole-[3,4-b]-indole de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2bde6e92981ffe7faf4bb30e52ede00
https://doi.org/10.1016/s0040-4020(01)93459-3
https://doi.org/10.1016/s0040-4020(01)93459-3
Publikováno v:
Journal of Heterocyclic Chemistry. 12:581-583
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::707924b07164adcaf13064eb0bc5e104
https://doi.org/10.1002/jhet.5570120329
https://doi.org/10.1002/jhet.5570120329