Feroniellic acids A-C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida

Three new isomeric furanocoumarins named feroniellic acids A-C (1-3) were isolated from the BuOH extract of Feroniella lucida roots. They are diastereomerically different to each other in configuration at C-2″ and C-3″. The structures were elucidated on the basis of spectroscopic data while their co...

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Main Authors: Preecha Phuwapraisirisan, Chalouyluk Phoopichayanun, Butsarakham Supudompol
Other Authors: Mahidol University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/18921
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spelling th-mahidol.189212018-07-12T09:50:56Z Feroniellic acids A-C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida Preecha Phuwapraisirisan Chalouyluk Phoopichayanun Butsarakham Supudompol Mahidol University Phetchaburi Rajabhat University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Three new isomeric furanocoumarins named feroniellic acids A-C (1-3) were isolated from the BuOH extract of Feroniella lucida roots. They are diastereomerically different to each other in configuration at C-2″ and C-3″. The structures were elucidated on the basis of spectroscopic data while their configurations were established by synthesis of model compounds together with application of Mosher's method. © 2008 Elsevier Ltd. All rights reserved. 2018-07-12T02:18:40Z 2018-07-12T02:18:40Z 2008-05-05 Article Tetrahedron Letters. Vol.49, No.19 (2008), 3133-3136 10.1016/j.tetlet.2008.03.027 00404039 2-s2.0-41649118612 https://repository.li.mahidol.ac.th/handle/123456789/18921 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=41649118612&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
Preecha Phuwapraisirisan
Chalouyluk Phoopichayanun
Butsarakham Supudompol
Feroniellic acids A-C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida
description Three new isomeric furanocoumarins named feroniellic acids A-C (1-3) were isolated from the BuOH extract of Feroniella lucida roots. They are diastereomerically different to each other in configuration at C-2″ and C-3″. The structures were elucidated on the basis of spectroscopic data while their configurations were established by synthesis of model compounds together with application of Mosher's method. © 2008 Elsevier Ltd. All rights reserved.
author2 Mahidol University
author_facet Mahidol University
Preecha Phuwapraisirisan
Chalouyluk Phoopichayanun
Butsarakham Supudompol
format Article
author Preecha Phuwapraisirisan
Chalouyluk Phoopichayanun
Butsarakham Supudompol
author_sort Preecha Phuwapraisirisan
title Feroniellic acids A-C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida
title_short Feroniellic acids A-C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida
title_full Feroniellic acids A-C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida
title_fullStr Feroniellic acids A-C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida
title_full_unstemmed Feroniellic acids A-C, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from Feroniella lucida
title_sort feroniellic acids a-c, three new isomeric furanocoumarins with highly hydroxylated geranyl derived moieties from feroniella lucida
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/18921
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