Chemical constituents from Piper marginatum Jacq. (Piperaceae)-antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435)
dc.contributor.author | Reigada J.B. | |
dc.contributor.author | Tcacenco Celize.M. | |
dc.contributor.author | Andrade L.H. | |
dc.contributor.author | Kato M.J. | |
dc.contributor.author | Porto A.L.M. | |
dc.contributor.author | Lago J.H.G. | |
dc.date.accessioned | 2024-03-13T01:39:53Z | |
dc.date.available | 2024-03-13T01:39:53Z | |
dc.date.issued | 2007 | |
dc.description.abstract | The leaves of Piper marginatum contain the antifungal compounds 3,4-methylenedioxypropiophenone 1, 2-methoxy-4,5-methylenedioxypropiophenone 2, 1-(3,4-methylenedioxyphenyl)propan-1-ol 3 (marginatumol), 5,4′-dihydroxy-7-methoxyflavanone 4 and 5,7-dihydroxy-4′-methoxyflavanone 5. The absolute configuration of natural marginatumol was determined as (+)-(R)-3 (ee 48%) by comparison of its optical properties with the chiral forms obtained by kinetic resolution of racemic 3 using Candida antarctica lipase (Novozym 435). © 2007 Elsevier Ltd. All rights reserved. | |
dc.description.firstpage | 1054 | |
dc.description.issuenumber | 9 | |
dc.description.lastpage | 1058 | |
dc.description.volume | 18 | |
dc.identifier.doi | 10.1016/j.tetasy.2007.05.006 | |
dc.identifier.issn | 0957-4166 | |
dc.identifier.uri | https://dspace.mackenzie.br/handle/10899/37649 | |
dc.relation.ispartof | Tetrahedron Asymmetry | |
dc.rights | Acesso Restrito | |
dc.title | Chemical constituents from Piper marginatum Jacq. (Piperaceae)-antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435) | |
dc.type | Artigo | |
local.scopus.citations | 30 | |
local.scopus.eid | 2-s2.0-34249864780 | |
local.scopus.updated | 2024-05-01 | |
local.scopus.url | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34249864780&origin=inward |