Ent-labdane-type diterpene glucosides from leaves of Rubus chingii (Q104971169)

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2980393-3

main subject

Rubus chingii var. suavissimus

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QIOMMMCQFIBVKA-NARXWROJSA-N

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(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1S,4aS,5R,8aS)-1,4a-dimethyl-5-[(3E)-3-methyl-5-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pent-3-en-1-yl]-6-methylidene-hexahydro-2H-naphthalene-1-carboxylate

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(2R,3R,4S,5S,6R)-2-[[(1S,2R,4aS,5R,8aR)-2-hydroxy-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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(2R,3R,4S,5S,6R)-2-[(E)-5-[(1R,4aR,5S,8aS)-5,8a-dimethyl-2-methylidene-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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inferred from

reverse claim

(2R,3R,4S,5S,6R)-2-[(E)-5-[(1R,4aR,5S,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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Takashi Tanaka

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ORCID Public Data File 2021

author name string

Keiko Kawamura

2

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2980393-3

Takumi Kitahara

3

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2980393-3

Hiroshi Kohda

4

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2980393-3

Osamu Tanaka

5

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2980393-3

publication date

January 1984

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16 September 2022

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2980393-3

volume

23

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2980393-3

issue

3

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2980393-3

page(s)

615-621

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2980393-3

cites work

Rubusoside (.BETA.-D-glucosyl ester of 13-O-.BETA.-D-glucosyl-steviol),a sweet principle of Rubus chingii Hu (Rosaceae).

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https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2980393-3

7 January 2021

Sweet and bitter glycosides of the Chinese plant drug, Bai-Yun-Shen (roots of Salvia digitaloides).

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2980393-3

7 January 2021

Isolation of trilobatin, a sweet dihydrochalcone-glucoside from leaves of Vitis piasezkii MAXIM. and V. saccharifera MAKINO.

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https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2980393-3

7 January 2021

Enzymatic hydrolysis of Ginseng saponins and their related glycosides (author's transl)

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https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2980393-3

7 January 2021

A diterpene glycoside and lignans from seed of Thujopsis dolabrata

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https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2980393-3

7 January 2021

Structures of stevia diterpene-glucosides : Application of 13C NMR

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https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2980393-3

7 January 2021

Studies on the constituents of Clematis species. V. On the saponins of the root of Clematis chinensis Osbeck. (5).

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7 January 2021

Saponin and sapogenol. XXXI. Chemical constituents of the seeds of Vigna angularis (Willd.) Ohwi et Ohashi. (1). Triterpenoidal sapogenols and 3-furanmethanol .BETA.-D-glucopyranoside.

1 reference

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7 January 2021