Zobrazeno 1 - 10
of 137
pro vyhledávání: '"Bruno Rindone"'
Publikováno v:
Molecules, Vol 13, Iss 1, Pp 129-148 (2008)
Enantiopure chiral amidic derivatives of sinapic acid were oxidised withhydrogen peroxide using horseradish peroxidase (HRP) as the catalyst to give thearyltetraline dilignol thomasidioic acid. Trans-diastereoselectivity and enantioselectivity inthe
Externí odkaz:
https://doaj.org/article/f8218b1ff4174316965559e1cf7d7d9d
Autor:
Ricardo Suarez-Bertoa, Michol Rindone, Francesco Saliu, Luca Zoia, Marco Orlandi, Bruno Rindone, Maurizio Bruschi, Eva Liisa Tollpa
Publikováno v:
Biomimetics Learning from Nature
Organic compounds obtained from radical coupling of phenylpropenoidic phenols have an important biological role. In fact, they constitute organic polymers such as lignin (Higuchi,1985) lignans (Ayers & Loike, 1990), suberin (Berdards et al. 1995) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25ae052b424ef2e4189e087c35d549a7
http://www.intechopen.com/articles/show/title/podophyllotoxin-and-antitumor-synthetic-aryltetralines-toward-a-biomimetic-preparation
http://www.intechopen.com/articles/show/title/podophyllotoxin-and-antitumor-synthetic-aryltetralines-toward-a-biomimetic-preparation
Publikováno v:
Synthetic Communications. 43:749-757
3-Benzyl-5-methyl-1,3-oxazolidine-3,4-diones react with Grignard reactants and with lithium alkyls to yield 4-substituted 3-benzyl-4-hydroxy-5-methyl-1,3-oxazolidine-2-ones. The reaction is stereoselective and follows Cram's rule.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d85693455d96cb03764fcfcd47b931f4
https://doi.org/10.1080/00397911.2011.609301
https://doi.org/10.1080/00397911.2011.609301
Autor:
Eeva-Liisa Tolppa, Marco Orlandi, Francesco Saliu, Bruno Rindone, Ricardo Suarez-Bertoa, Guido Galliani
Publikováno v:
Synthetic Communications. 41:956-962
(Chemical Equation Presented) The reaction between aliphatic amines and propylene carbonate can be performed in solventless conditions under microwave irradiation, becoming nearly complete within 15 min of irradiation. Oxidation of the formed mixture
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20016f2e4dd8e289ff70271b25ff683b
https://doi.org/10.1080/00397911003707154
https://doi.org/10.1080/00397911003707154
Autor:
Bruno Rindone, Maurizio Bruschi, Jens Hjorth, Marco Orlandi, Guido Galliani, Ezio Bolzacchini
Publikováno v:
Journal of Physical Organic Chemistry. 19:570-578
Product studies, kinetic isotope effect measurements, linear free energy relationships and calculations have been used to study the NO3-promoted nitration of toluene and phenol in presence of NO2. The competition between of a rate-determining hydroge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72aa88096eab6aab65009cb74722f558
https://doi.org/10.1002/poc.1060
https://doi.org/10.1002/poc.1060
Autor:
Vito Librando, Simone Meinardi, Bruno Rindone, Ezio Bolzacchini, Marco Orlandi, Claudio Scicali, Barbara Barletta
Publikováno v:
Ozone: Science & Engineering. 24:271-280
Five azaarenes were oxidized with ozone. The rate constant was measured for three of them. Product studies showed that ring fragmentation occurs with phenanthrolines, acridine and phenazine. Ring fragmentation and oxygen insertion is observed with ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8df880f462bf9789c5f31d68e307289a
https://doi.org/10.1080/01919510208901618
https://doi.org/10.1080/01919510208901618
Publikováno v:
Tetrahedron. 57:371-378
Stereoselective bimolecular radical coupling of enantiopure phenylpropenoidic phenols are described, starting from enantiopure amidic derivatives of ferulic acid. The latter were prepared from ferulic acid by reaction with (S)-alanine or Oppolzer cam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cca035a8fe467a03e70b1e20b2dc9ea3
https://doi.org/10.1016/s0040-4020(00)00944-3
https://doi.org/10.1016/s0040-4020(00)00944-3
Publikováno v:
Tetrahedron Letters. 50:5123-5125
Diazabicyclo[5.4.0]undecene (DBU) reacts with carbon dioxide and N-subsititued-2-chloroacetoamides in a very simple one-step procedure, to give the corresponding 3-substituted oxazolidin-2,4-diones in excellent yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d523ce3821ec0f75847076138a220b2
https://doi.org/10.1016/j.tetlet.2009.06.109
https://doi.org/10.1016/j.tetlet.2009.06.109
Publikováno v:
Chemical Physics Letters. 309:364-368
Fourier-transformed infrared spectroscopy (FT-IR) was used to determine the rate constants and products for the reactions of tetrafluoroethylene (C 2 F 4 ) with OH, NO 3 and O 3 at 298±4 K and 740±5 Torr. The rate constants ( k ) measured were: k C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5824aed30b29ae156407c037c818c60
https://doi.org/10.1016/s0009-2614(99)00698-3
https://doi.org/10.1016/s0009-2614(99)00698-3
Publikováno v:
Aarhus University
Cavalli, F, Glasius, M, Hjorth, J L, Rindone, B & Jensen, N R 1998, ' Atmospheric lifetimes, infrared spectra and degradation products of a series of hydrofluoroethers ', Atmospheric Environment, vol. 32, pp. 3767-3773 .
Cavalli, F, Glasius, M, Hjorth, J L, Rindone, B & Jensen, N R 1998, ' Atmospheric lifetimes, infrared spectra and degradation products of a series of hydrofluoroethers ', Atmospheric Environment, vol. 32, pp. 3767-3773 .
The rate constants of the reactions between the OH radical and a series of hydrofluoroethers (HFE) have been measured. The reaction of OH with CHF 2 OCF 2 OCHF 2 (1), CHF 2 OCF 2 CF 2 OCHF 2 (2), CHF 2 OCF 2 CF 2 OCF 2 OCHF 2 (3) and CH 3 OC 4 F 9 (4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8db6ba290cfc4a9eaeff1edeb29f2e57
https://doi.org/10.1016/s1352-2310(98)00106-x
https://doi.org/10.1016/s1352-2310(98)00106-x