Phenolic Compounds from the Fresh Leaves of Eucalyptus maideni (Q118256187)

http://api.crossref.org/works/10.1002%2Fhlca.201000067

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[2,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxybenzoyl)oxyoxan-3-yl] 3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoate

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(3,4,5,12,13,21,22,23-Octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl) 3,4,5-trihydroxybenzoate

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4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one

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beta-D-Glucopyranose, 6-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)-

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2,3,5-Trihydroxy-6-(hydroxymethyl)oxan-4-yl 3,4,5-trihydroxybenzoate

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6-[[3,4,12,13,21,22,23-Heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-5-yl]oxy]-2,3,4-trihydroxybenzoic acid

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3-(3,4,5,11,17,18,19-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl)-3-hydroxy-2-(3,4,5-trihydroxybenzoyl)oxypropanoic acid

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2-[[2-(3,4-dihydroxyphenyl)-3-hydroxy-7-methoxy-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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4,6-Dihydroxy-3-methyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzaldehyde

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2-[4-[6-(1,3-Benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-hydroxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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1-[6-[3,4-Dihydroxy-6-(hydroxymethyl)-5-methyloxan-2-yl]oxy-2,4-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methylbutan-1-one

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[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate

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Li-Wen Tian

1

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http://api.crossref.org/works/10.1002%2Fhlca.201000067

Chong-Ren Yang

series ordinal

2

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.201000067

Ying-Jun Zhang

series ordinal

3

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http://api.crossref.org/works/10.1002%2Fhlca.201000067

publication date

November 2010

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16 September 2022

Helvetica Chimica Acta

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http://api.crossref.org/works/10.1002%2Fhlca.201000067

volume

93

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http://api.crossref.org/works/10.1002%2Fhlca.201000067

issue

11

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http://api.crossref.org/works/10.1002%2Fhlca.201000067

page(s)

2194-2202

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http://api.crossref.org/works/10.1002%2Fhlca.201000067

cites work

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Synthesis of optically active vomifoliol and roseoside stereoisomers

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Two acylated flavonol glycosides from Eucalyptus rostrata

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Bioactive acylphloroglucinol derivatives from Eucalyptus species

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Lignans from Apollonias barbujana

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Phloroglucinol compounds of natural origin

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Inhibitors of skin-tumor promotion. VIII. Inhibitory effects of euglobals and their related compounds on Epstein-Barr virus activation. (1).

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Triterpenoids from the Leaves ofEucalyptus camaldulensisvar.obtusa

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Eucalbanins A,B and C, Monomeric and Dimeric Hydrolyzable Tannins from Eucalyptus alba REINW.

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Phloroglucinol glycosides from the fresh fruits of Eucalyptus maideni

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Gemins D, E and F, ellagitannins from Geum japonicum

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Bioactive monoterpene glycosides conjugated with gallic acid from the leaves of Eucalyptus globulus

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Tannins of cornaceous plants. I. Cornusiins A, B and C, dimeric monomeric and trimeric hydrolyzable tannins from Cornus officinalis, and orientation of valoneoyl group in related tannins

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Polyphenols from Eucalyptus ovata.

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Resveratrol/phloroglucinol glycosides from the roots of Lysidice rhodostegia

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Eucalmaidins A-E, (+)-oleuropeic acid derivatives from the fresh leaves of Eucalyptus maideni

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/HLCA.201000067

Identifiers

DOI

10.1002/HLCA.201000067

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