Zobrazeno 1 - 10
of 16
pro vyhledávání: '"faveline"'
Autor:
Paulo Fernando Machado Paredes, Selene Maia de Morais, Fernando César Rodrigues Brito, Luiz Francisco Wemmenson Gonçalves Moura, Patrícia de Araújo Rodrigues, Stephen Rathinaraj Benjamin, Francisco Ernani Alves Magalhães, Eridan Orlando Pereira Tramontina Florean, Maria Izabel Florindo Guedes
Publikováno v:
Asian Pacific Journal of Tropical Biomedicine, Vol 8, Iss 7, Pp 345-351 (2018)
Objective: To evaluate the chemical components of active extract from Cnidoscolus quercifolius root bark and its cytotoxic potential against several tumor strains. Methods: The high-performance liquid chromatography with diode-array detection and 1H
Externí odkaz:
https://doaj.org/article/b66b989d938a46108a73ac2f4cd1a335
Autor:
Luiz Francisco Wemmenson Gonçalves Moura, Francisco Ernani Alves Magalhães, Maria Izabel Florindo Guedes, Stephen Rathinaraj Benjamin, Fernando César Rodrigues Brito, Eridan Orlando Pereira Tramontina Florean, Selene Maia de Morais, Patrícia de Araújo Rodrigues, Paulo Fernando Machado Paredes
Publikováno v:
Asian Pacific Journal of Tropical Biomedicine, Vol 8, Iss 7, Pp 345-351 (2018)
Objective: To evaluate the chemical components of active extract from Cnidoscolus quercifolius root bark and its cytotoxic potential against several tumor strains. Methods: The high-performance liquid chromatography with diode-array detection and 1H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fed5920ee1b92fb5ca0ad2beecde08b
https://doi.org/10.4103/2221-1691.237077
https://doi.org/10.4103/2221-1691.237077
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Chun-Kuei Chen, Tse‐Lok Ho
Publikováno v:
Tetrahedron. 51:5819-5824
A convergent approach to faveline methyl ether based on Claisen rearrangement is delineated. Thus the benzylic and allylic alcohol substrate was assembled by a Grignard reaction, and the rearrangement product was oxidized and cyclized. Double bond is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b228a4799f7ad71d768f7c96693d7b63
https://doi.org/10.1016/0040-4020(95)00240-9
https://doi.org/10.1016/0040-4020(95)00240-9
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :327-332
Simple and efficient syntheses have been developed for the cytotoxic dinorditerpenoids, (±)-deoxofaveline 1, (±)-faveline methyl ether 2 and (±)-faveline 3, having a hexahydrodibenzo[a,d]cycloheptene ring system, through the enolizable tricyclic k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edbb5cb336ad6adeedc8e889cb37b601
https://doi.org/10.1039/p19940000327
https://doi.org/10.1039/p19940000327
Publikováno v:
ChemInform. 25
Simple and efficient syntheses have been developed for the cytotoxic dinorditerpenoids, (±)-deoxofaveline 1, (±)-faveline methyl ether 2 and (±)-faveline 3, having a hexahydrodibenzo[a,d]cycloheptene ring system, through the enolizable tricyclic k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2e2aa1ab56c67a7e6e4d8ab6d13918a
https://doi.org/10.1002/chin.199422213
https://doi.org/10.1002/chin.199422213
Autor:
Tse‐Lok Ho, Chun-Kuei Chen
Publikováno v:
ChemInform. 26
A convergent approach to faveline methyl ether based on Claisen rearrangement is delineated. Thus the benzylic and allylic alcohol substrate was assembled by a Grignard reaction, and the rearrangement product was oxidized and cyclized. Double bond is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::062918ae0d2d41af32ea7e61c32d781c
https://doi.org/10.1002/chin.199537222
https://doi.org/10.1002/chin.199537222
Publikováno v:
Tetrahedron Letters. 33:655-658
Simple and efficient syntheses of the cytotoxic benzocycloheptenes (±)-deoxofaveline(1) and (±)-faveline methyl ether(2) have been developed by a convergent route from the ketone 7 via the tricyclic ketone12.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e2eb61d1523572a520f60015b40ef55
https://doi.org/10.1016/s0040-4039(00)92335-9
https://doi.org/10.1016/s0040-4039(00)92335-9
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae8bc7359ce6cbeecf79298084bf671b
https://doi.org/10.1002/chin.200606191
https://doi.org/10.1002/chin.200606191
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.