DSpace JSPUI
DSpace preserves and enables easy and open access to all types of digital content including text, images, moving images, mpegs and data sets
Learn More
Please use this identifier to cite or link to this item:
https://repositorio.ufba.br/handle/ri/3829| metadata.dc.type: | Artigo de Periódico |
| Title: | Determinação da Estereoquímica Relativa de Pimaradienos Através de Produtos de Oxidação |
| Other Titles: | Química Nova |
| Authors: | Cruz, Frederico Guare Roque, Nídia Franca |
| metadata.dc.creator: | Cruz, Frederico Guare Roque, Nídia Franca |
| Abstract: | Relative stereochemistry determination of pimaradienes through oxidative products. Pimaradienes, including isopimaradienes, with an endocyclic double bond between C-9 and C-11 are uncommon compounds in nature. The diterpenoid pimar-9(11),15-dien-19-oic acid (1) was isolated from Mikania triangularis (Asteraceae) and the correct stereochemistry of 1was established by 1H and 13C NMR studies of several oxidative products, mainly epoxides, of this compound and its double bond isomers. |
| Keywords: | Diterpenes Pimaradienes Stereochemistry |
| URI: | http://www.repositorio.ufba.br/ri/handle/ri/3829 |
| Issue Date: | 1997 |
| Appears in Collections: | Artigo Publicado em Periódico (Química) |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.