(Q104972255)

http://api.crossref.org/works/10.1002%2Fhlca.200890118

1 reference

1 reference

2-hexyl-5-hydroxy-7-methoxychromen-4-one

1 reference

(2S)-2-(dimethylamino)-3-methyl-N-[(3S,4S,7S,10Z)-7-(2-methylpropyl)-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]butanamide

1 reference

(2S,3R,4R,5R,6S)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-methyloxane-3,4,5-triol

1 reference

(1R,2R,5R,6S,7S,10S,14R,15R,16S,21R)-6,7,16-trihydroxy-1,2,5,8,8,15,20,20-octamethyl-19-oxapentacyclo[12.9.0.02,11.05,10.015,21]tricos-11-ene-18,23-dione

1 reference

(8S,8aR)-5-[(2S)-1-hydroxypropan-2-yl]-3,8-dimethyl-6,7,8,8a-tetrahydro-1H-azulen-2-one

1 reference

(8S,8aR)-3,8-dimethyl-5-propan-2-yl-1,7,8,8a-tetrahydroazulene-2,6-dione

1 reference

1 reference

(6R,8S,8aR)-6-hydroxy-3,8-dimethyl-5-propan-2-yl-6,7,8,8a-tetrahydro-1H-azulen-2-one

1 reference

Tiliaceae

1 reference

1

Serge Michalet

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

author name string

Laëtitia Payen‐Fattaccioli

2

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

Chantal Beney

3

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

Pascale Cégiéla

4

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

Christine Bayet

5

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

Gilbert Cartier

6

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

Diderot Noungoué‐Tchamo

7

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

Etienne Tsamo

8

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

Anne‐Marie Mariotte

9

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

Marie‐Geneviève Dijoux‐Franca

10

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

publication date

June 2008

1 reference

16 September 2022

Helvetica Chimica Acta

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

volume

91

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

issue

6

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

page(s)

1106-1117

1 reference

http://api.crossref.org/works/10.1002%2Fhlca.200890118

cites work

Circumscription of Malvaceae (Malvales) as Determined by a Preliminary Cladistic Analysis of Morphological, Anatomical, Palynological, and Chemical Characters

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Phylogeny of the core Malvales: evidence from ndhF sequence data.

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Anti-carcinogenic activity of Taraxacum plant. II.

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

New cyclopeptide alkaloids from Melochia tomentosa

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Analysis of metabolic pathways via quantitative prediction of isotope labeling patterns: a retrobiosynthetic 13C NMR study on the monoterpene loganin

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

New Bis-Iridoids from Dipsacus laciniatus

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Lycium chinense, III: isolation of scopoletin and vanillic acid (author's transl)

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

A Novel Lignan and Flavonoids from Polygonum aviculare

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Plant anticancer agents XXIX. Cleomiscosin A from Simaba multiflora, Soulamea soulameoides, and Matayba arborescens

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Tyrosinase inhibitors from Rhododendron collettianum and their structure-activity relationship (SAR) studies.

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Structures of cleomiscosins, coumarinolignoids of cleome viscosa seeds

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Chemical constituents from the peels of Citrus sudachi

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Glucosides of acidic limonoids in citrus

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

A chromone from Zanthoxylum species

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Alkyl, aryl, alkylarylquinoline, and related alkaloids

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Antimitotic activity of 5-hydroxy-7-methoxy-2-phenyl-4-quinolones.

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

A cyperane and trixanes from Jungia polita

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Daucane sesquiterpenes from Ferula hermonis

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Anti-inflammatory activity of new guaiane type sesquiterpene from Wikstroemia indica.

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Guaiane- and aristolane-type sesquiterpenoids of Nardostachys chinensis roots

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Medicinal foodstuffs. XXVIII. Inhibitors of nitric oxide production and new sesquiterpenes, zedoarofuran, 4-epicurcumenol, neocurcumenol, gajutsulactones A and B, and zedoarolides A and B, from Zedoariae Rhizoma

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Dictamnol, a New Trinor-Guaiane Type Sesquiterpene, from the Roots of Dictamnus dasycarpus Turcz.

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Sesqui- and diterpenoids from Ptilidium ciliare and Barbilophozia species (liverworts)

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Isoreiswigin, a New Diterpene from a Marine Sponge

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Guaiane dimers from Xylopia vielana

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Bioactive 12-oleanene triterpene and secotriterpene acids from Maytenus undata.

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Secomultiflorane-type triterpenoid acids from stem bark of Sandoricum koetjape

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

A-seco-oleane-type triterpene acids from Ligularia intermedia

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

A seco-olean-18-ene triterpene acid from Vahlia capensis

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Bioassay-guided isolation of antifungal alkaloids from Melochia odorata

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Cyclopeptide alkaloids

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021

Two cyclopeptide alkaloids from Zizyphus lotus

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.200890118

7 January 2021