A new alkaloid of Strychnos. The ocurrence of 11-methoxy-diaboline in Strychnos romeu-belenii Krukoff and Barneby
Author | dc.contributor.author | Marini-Bettòlo, G. B. | |
Author | dc.contributor.author | Delle Monache, E. M. | es_CL |
Author | dc.contributor.author | Erazo, Silvia | es_CL |
Author | dc.contributor.author | Galeffi, Corrado | es_CL |
Admission date | dc.date.accessioned | 2011-03-16T14:38:54Z | |
Available date | dc.date.available | 2011-03-16T14:38:54Z | |
Publication date | dc.date.issued | 1971 | |
Cita de ítem | dc.identifier.citation | Gazzetta Chimica Italiana 111: 971-980 | en_US |
Identifier | dc.identifier.issn | 0016-5603 | |
Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/121156 | |
Abstract | dc.description.abstract | From the stem bark of Strychnos romeu-belenii Krukoff and Barneby, a Longaniacea of South America, a new indolinic alkaloid has been isolated to which the structure of 11-,11-methoxy-diaboline(I) has been assigned on the basis of UV, IR, NMR, ORD and MS data. The structure was confirmed by converting(I) into α-colubrine(II) (11-methoxy-strychnine) through the N-deacetyl-derivative(III) (11-methoxy-Wieland-Gumlich aldehyde). (I) by acetylation gives the isomer C-17 of condensamine (IV) for which we propose the name isocondensamine(v). In addition, 11-methoxy-Wieland-Gumlich aldehyde(III) yields on heating with acetic acid and sodium acetate the dimeric 11,11'-dimethoxy-caracurine v (vi). | en_US |
Lenguage | dc.language.iso | en | en_US |
Publisher | dc.publisher | Societá Chimica Italiana | en_US |
Keywords | dc.subject | Strychnos | en_US |
Título | dc.title | A new alkaloid of Strychnos. The ocurrence of 11-methoxy-diaboline in Strychnos romeu-belenii Krukoff and Barneby | en_US |
Document type | dc.type | Artículo de revista |
Files in this item
This item appears in the following Collection(s)
-
Artículos de revistas
Artículos de revistas