dc.creator | de Fatima, A | |
dc.creator | Kohn, LK | |
dc.creator | Antonio, MA | |
dc.creator | de Carvalho, JE | |
dc.creator | Pilli, RA | |
dc.date | 2005 | |
dc.date | APR 15 | |
dc.date | 2014-11-14T14:08:53Z | |
dc.date | 2015-11-26T17:15:09Z | |
dc.date | 2014-11-14T14:08:53Z | |
dc.date | 2015-11-26T17:15:09Z | |
dc.date.accessioned | 2018-03-29T00:03:24Z | |
dc.date.available | 2018-03-29T00:03:24Z | |
dc.identifier | Bioorganic & Medicinal Chemistry. Pergamon-elsevier Science Ltd, v. 13, n. 8, n. 2927, n. 2933, 2005. | |
dc.identifier | 0968-0896 | |
dc.identifier | WOS:000228254000021 | |
dc.identifier | 10.1016/j.bmc.2005.02.007 | |
dc.identifier | http://www.repositorio.unicamp.br/jspui/handle/REPOSIP/52443 | |
dc.identifier | http://www.repositorio.unicamp.br/handle/REPOSIP/52443 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/52443 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1281974 | |
dc.description | The total syntheses of (R)-goniothalamin (1), a styryl lactone isolated from several Goniothalamus species, via catalytic asymmetric allylation of alpha-benzyloxyacetaldehyde (2), followed by ring-closing metathesis and Wittig olefination and via catalytic asymmetric allylation of trans-cinnamaldehyde (12), followed by ring-closing metathesis are reported. The anti proliferative activities of (R)-1 and its Z-isomer 10 as well as of the synthetic dihydropyranone intermediates 7 and 8 against eight different cancer cell lines are also described. (c) 2005 Elsevier Ltd. All rights reserved. | |
dc.description | 13 | |
dc.description | 8 | |
dc.description | 2927 | |
dc.description | 2933 | |
dc.language | en | |
dc.publisher | Pergamon-elsevier Science Ltd | |
dc.publisher | Oxford | |
dc.publisher | Inglaterra | |
dc.relation | Bioorganic & Medicinal Chemistry | |
dc.relation | Bioorg. Med. Chem. | |
dc.rights | fechado | |
dc.rights | http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy | |
dc.source | Web of Science | |
dc.subject | (R)-goniothalamin | |
dc.subject | asymmetric synthesis | |
dc.subject | cytotoxic activity | |
dc.subject | cancer cells | |
dc.subject | Catalytic Asymmetric Allylation | |
dc.subject | Mevinic Acid Analogs | |
dc.subject | Chiral Lewis-acid | |
dc.subject | Enantioselective Syntheses | |
dc.subject | Bis(((s)-binaphthoxy)(isopropoxy)titanium) Oxide | |
dc.subject | Alternative Approach | |
dc.subject | Organic-synthesis | |
dc.subject | Formal Synthesis | |
dc.subject | Benzyl Ethers | |
dc.subject | Goniothalamin | |
dc.title | (R)-goniothalamin: total syntheses and cytotoxic activity against cancer cell lines | |
dc.type | Artículos de revistas | |