Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sergio Crippa"'
Publikováno v:
Tetrahedron. 70:3994-4001
A simple, efficient and general two step procedure, through a sequential Ugi reaction followed by a Bischler–Napieralski/heterocyclization tandem closure, to give novel 6,11-dihydro-5H-imidazo[1′,5′:1,2]pyrido[3,4-b]indol-2-ium salt derivatives
Autor:
Sergio Crippa, Bruno Danieli, Giovanna Pressi, Anacleto Minghetti, Fabiana Antognoni, Ferruccio Poli, Roberto Dal Toso, Nicoletta Crespi Perellino
Publikováno v:
Fitoterapia. 82:950-954
3,5-O-dicaffeoyl-4-O-malonilquinic acid (1) (irbic acid) has been isolated for the first time from cell cultures of Centella asiatica and till now it has never been reported to be present in the intact plant. Evidence of its structure was obtained by
Autor:
Andrea Virdis, Alessandro Sacchetti, Alessandra Silvani, Daniele Passarella, Bruno Danieli, Sergio Crippa, Giordano Lesma
Publikováno v:
Tetrahedron. 60:6437-6442
A ruthenium-catalyzed ring opening–ring closing metathesis reaction serves as the key step in the stereoselective synthesis of a new enantiopure 2-substituted-4,5-dehydropiperidine skeleton, a valuable intermediate for the synthesis of piperidine a
Publikováno v:
ChemInform. 45
A simple, efficient and general two step procedure, through a sequential Ugi reaction followed by a Bischler–Napieralski/heterocyclization tandem closure, to give novel 6,11-dihydro-5H-imidazo[1′,5′:1,2]pyrido[3,4-b]indol-2-ium salt derivatives
Publikováno v:
Fitoterapia. 75(5)
Two new compounds, 10-O-beta-D-glucopyranosyl aloenin (4) and 8-C-beta-D-glucopyranosyl-7-O-methyl-(R)-aloesol (6), were isolated from a commercial sample of Kenya aloe together with the known products aloenin (2), aloenin 2'-p-coumaroyl ester (3), a
Autor:
Fiorella Meneghetti, Giordano Lesma, Sergio Crippa, Manuele Musolino, Alessandra Silvani, Alessandro Sacchetti, Paola Giovanelli, Roberto Cecchi
Publikováno v:
Organic & Biomolecular Chemistry. 10:9004
We report here a two step efficient route for the synthesis of 1,2,3,4-tetrahydro-β-carboline (THBC)-based tetracyclic peptidomimetics from a Ugi 4-CR/Pictet-Spengler reaction sequence. Suitably N-protected 2-aminoacetaldehyde was for the first time
Autor:
Sergio Crippa, Paola Cairoli, Carlo F. Morelli, Paolo Manitto, Giovanna Speranza, Daniela Monti
Publikováno v:
Natural Product Communications. 1:1934578X0600101
A new naphthalene O,O,O-triglycoside, kenyaloside (1), was isolated from the dried exudate of Kenyan Aloe species, a bittering and laxative agent. Its structure was established by combined spectral and chemical methods as 1-(β-D-glucopyranosyloxy)-8
Publikováno v:
Journal of Chemical Research. :160
1 H and 13 C NMR spectra were obtained for a series of sixteen paramagnetic complexes of general formula [CoX 2 LO 2 ], where X is Cl or Br and L is a methylpyridine (picoline) or a dimethylpyridine (lutidine); use of inverse NMR and heteronuclear co
Autor:
Sergio Crippa, Vittorio Vecchietti, Giordano Lesma, Giovanni Palmisano, Daniele Passarella, Bruno Danieli
Publikováno v:
Scopus-Elsevier
Four natural N-methylindolines have been isolated from the roots of Vinca sardoa (Stearn) Pignati. They are ent-N(1)-methyl-14,15-didehydroaspidospermidine (7),N(1)-methyl-14,15-didehydroaspidofractinine (10), N(1)-methylaspidofractinine (11) and N(1
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https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59645b0e1b662fb36f4c6c3ccdf97fbe
http://www.scopus.com/inward/record.url?eid=2-s2.0-0001477415&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0001477415&partnerID=MN8TOARS