101. Constituintes qu?micos isolados das cascas de Simira glaziovii (Rubiaceae)
- Author
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Bastos, Ana Beatriz Farias D' Oliveira, Carvalho, Mario Geraldo de, Alves, H?lio de Mattos, Sant'Anna, Carlos Maur?cio de, and M?rcia Cristina Campos, Oliveira
- Subjects
Qu?mica - Abstract
Submitted by Celso Magalhaes (celsomagalhaes@ufrrj.br) on 2020-11-26T15:09:42Z No. of bitstreams: 1 2001 - Ana Beatriz Farias D'Oliveira Bastos.pdf: 13367000 bytes, checksum: 779af4e670ada212c1d61ee4a5e55504 (MD5) Made available in DSpace on 2020-11-26T15:09:42Z (GMT). No. of bitstreams: 1 2001 - Ana Beatriz Farias D'Oliveira Bastos.pdf: 13367000 bytes, checksum: 779af4e670ada212c1d61ee4a5e55504 (MD5) Previous issue date: 2001-02-12 Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES The phytochemical study of the bark of Simira glaziovii (Rubiaceae) afforded the sitostenone and estigmastenone isolated from hexanic extract and sitosterol, stigmasterol, methyl dimethoxy cynamate, the harman alkaloid and the new enantiomer of ophiorine B, (-)ophiorine B from methanolic extract. The structures of the compounds were established by IR, NMR and mass spectra analysis of the natural substances and derivatives. The methyl lialosilate of ophiorone B, after treatment with acetic anhydride and pyridine, yielded the tetraacetyl derivative. The same treatment of ophiorine B yielded two new acetyl derivatives, pentaacetyl lyalosidic acid and the ?-carboline monoterpene tetraacetyl glucoside (1,22-lactam-lyaloside) O estudo fitoqu?mico das cascas de Simira glaziovii conduziu ao isolamento e identifica??o dos ester?ides sitostenona e estigmastenona do extrato hex?nico; do extrato metan?lico foram isolados sitosterol, estigmasterol, 3,4-dimetoxicinamato de metila e dois alcal?ides ?-carbol?nicos harmana (9Hpirido[3,4b]indol) e um novo enanti?mero da ofiorina B, a (-)ofiorina B. As estruturas destas subst?ncias naturais foram determinadas com base na an?lise de espectros de IV, RMN e de massas. A rea??o da (-)ofiorina B com diazometano, forneceu o lialosilato de metila. Este ?ster met?lico foi tratado com anidrido ac?tico e piridina e forneceu o tetra-O-acetil lialosilato de metila. O mesmo tratamento da (-)ofiorina B forneceu dois novos derivados acetilados, o ?cido pentaacetil lialos?dico e o monoterpeno ?-carbol?nico, tetraacetil glicos?deo (1,22-lactamil-lialos?deo). ABSTRACT
- Published
- 2001