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| - wetenschappelijk artikel (nl)
- наукова стаття, опублікована в травні 1995 (uk)
- im Mai 1995 veröffentlichter wissenschaftlicher Artikel (de)
- artículu científicu espublizáu en mayu de 1995 (ast)
- scientific article published on 01 May 1995 (en)
- գիտական հոդված հրատարակված 1995 թվականի մայիսի 1-ին (hy)
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| - Y Miyata
- A Fujii
- Y Mimaki
- Y Sashida
- A Kameyama
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| - A novel hexahydrodibenzofuran derivative with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells from Lindera umbellata bark (en)
- A novel hexahydrodibenzofuran derivative with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells from Lindera umbellata bark (nl)
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| - A novel hexahydrodibenzofuran derivative with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells from Lindera umbellata bark (en)
- A novel hexahydrodibenzofuran derivative with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells from Lindera umbellata bark (nl)
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| name
| - A novel hexahydrodibenzofuran derivative with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells from Lindera umbellata bark (en)
- A novel hexahydrodibenzofuran derivative with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells from Lindera umbellata bark (nl)
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| title
| - A novel hexahydrodibenzofuran derivative with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells from Lindera umbellata bark (en)
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| is cites work
of | - Novel cytotoxic chalcones from Litsea rubescens and Litsea pedunculata.
- Chemical constituents of the stems and twigs of Lindera umbellata
- Melanin biosynthesis inhibitors from the bark of Machilus thunbergii
- Organocatalyzed Asymmetric Synthesis of Dihydrodibenzofurans Based on a Dienamine Process
- Electrochemical synthesis of selenyl-dihydrofurans via anodic selenofunctionalization of allyl-naphthol/phenol derivatives and their anti-Alzheimer activity
- Asymmetric total synthesis of (-)-Linderol A.
- First total synthesis of (+/-)-Linderol A, a tricyclic hexahydrodibenzofuran constituent of Lindera umbellata bark, with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells
- Novel stereoconvergent transformation of 1,2a-disubstituted 1,2,2a,8b-tetrahydro-3H-benzo[b]cyclobuta[d]pyran-3-ones to 1,3-disubstituted 1,2,4a,9b-tetrahydrodibenzofuran-4-ols and its application to the second-generation synthesis of (+/-)-linderol
- The first total synthesis of (+/-)-linderol A, a tricyclic hexahydrodibenzofuran constituent of Lindera umbellata bark, with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells
- Phosphine-catalysed asymmetric dearomative formal [4+2] cycloadditions of 3-benzofuranyl vinyl ketones
- Synthetic approaches to natural products containing 2,3-dihydrobenzofuran skeleton
- Improved enantioselective synthesis of (-)-linderol A: hindered rotation about aryl-Csp(3) bond.
- Synthesis of (±)-8-deisopropyladunctin B
- Asymmetric conjugate additions of 2-substituted benzofuran-3(2H)-ones to α,β-unsaturated ketones catalyzed by chiral copper complexes.
- Asymmetric dearomatic Diels-Alder reactions of diverse heteroarenes via π-system activation
- Enantioselective total syntheses of (+)-hostmanin A, (-)-linderol A, (+)-methyllinderatin and structural reassignment of adunctin E
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