Two isomeric epoxysitosterols from Rhododendron formosanum: 1H and 13C NMR chemical shift assignments (Q83841718)

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28 January 2020

title

Two isomeric epoxysitosterols from Rhododendron formosanum: 1H and 13C NMR chemical shift assignments (English)

1 reference

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[(3S,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-formyl-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate

28 January 2020

main subject

Rhododendron formosanum

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inferred from

reverse claim

alpha-Epoxysitostanol

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inferred from

reverse claim

(3R,3aR,5aS,5bR,9S,11aS,11bS,13aR,13bR)-3a,5a,8,8,11b,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,9,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-ol

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[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate

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Vivek Krishna

1

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28 January 2020

Chi-I Chang

series ordinal

2

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28 January 2020

Chang-Hung Chou

series ordinal

3

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Magnetic Resonance in Chemistry

28 January 2020

publication date

2006

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16 September 2022

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28 January 2020

volume

44

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28 January 2020

issue

8

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28 January 2020

page(s)

817-819

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Carbon-13 nmr studies on sitosterol biosynthesized from [13C]mevalonates

28 January 2020

cites work

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Crossref

https://api.crossref.org/works/10.1002%2FMRC.1844

Triterpenoids of the bark of Pieris japonica D. Don (Japanese name: asebi). II. 13C Nuclear magnetic resonance of the .GAMMA.-lactones of ursane- and oleanane-type triterpenes.

21 January 2018

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Crossref

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Two epimeric friedelane triterpenes isolated fromMaytenus truncata Reiss:1H and13C chemical shift assignments

21 January 2018

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Flavonoids from the root-bark of Dioclea grandiflora

1 reference

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Identifiers

DOI

10.1002/MRC.1844

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16724364%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

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