(Q104851267)

http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900352-5

main subject

Stenochlaena palustris

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beta-Sitosterol 3-O-beta-D-galactopyranoside

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(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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(4S,5R)-3,3,5-trimethyl-4-[(Z,2R,5S,13R)-5,9,10-trimethyl-8-oxo-2,13-bis[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]tetradec-9-en-5-yl]cyclohexan-1-one

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(2S,3S)-2,4,4-trimethyl-3-[(E,3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohexan-1-one

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Longan cerebroside II

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(4R,5S)-3,3,5-trimethyl-4-[(Z,2S,5R,13R)-5,9,10-trimethyl-8-oxo-2,13-bis[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]tetradec-9-en-5-yl]cyclohexan-1-one

indole-3-carboxaldehyde

1 reference

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Hongmei Liu

1

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900352-5

Jimmy Orjala

series ordinal

2

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900352-5

Topul Rali

series ordinal

3

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900352-5

Otto Sticher

series ordinal

4

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900352-5

publication date

December 1998

3 references

16 September 2022

16 September 2022

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900352-5

volume

49

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900352-5

issue

8

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900352-5

page(s)

2403-2408

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900352-5

cites work

Direct evidence by carbon-13 NMR spectroscopy for the erythro configuration of the sphingoid moiety in Gaucher cerebroside and other natural sphingolipids

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900352-5

7 January 2021

Biologically active glycosides from asteroidea, XX. Glycosphingolipids from the starfishAsterina pectinifera,1. Isolation and characterization of acanthacerebroside B and structure elucidation of related, nearly homogeneous cerebrosides

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900352-5

7 January 2021

Application of multilayer coil countercurrent chromatography for the study of Vitis vinifera cv. Riesling leaf glycosides

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900352-5

7 January 2021

3-formylindole from Murraya exotica

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900352-5

7 January 2021

Glycosidically Bound Norisoprenoids from Vitis vinifera cv. Riesling Leaves

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900352-5

7 January 2021

Marine Natural Products: 3-Formylindole from the Red Algae Botryocladia leptopoda

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900352-5

7 January 2021

Isolation of Indole-3-Aldehyde from Psuedomonas syringae pv. savastanoi

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900352-5

7 January 2021