(Q104936444)

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

1 reference

methyl (1R,13R,14R)-15-ethylidene-1-hydroxy-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate

1 reference

inferred from

reverse claim

(1S,10R,12R,13R,15R,16S,17R)-15-ethenyl-13-methyl-13-oxido-19-oxa-3-aza-13-azoniahexacyclo[14.3.1.02,10.04,9.010,15.012,17]icosa-2,4,6,8-tetraene

1 reference

1 reference

1 reference

(1R,2S,4S,7E,8S,9R)-7-ethylidene-1'-methoxy-5-methylspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one

1 reference

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(1'R,3S,4'S,7'Z,8'R,9'S)-7'-ethylidene-1-methoxy-5'-methyl-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-2-one

1 reference

1 reference

1 reference

Dhavadee Ponglux

1

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

Sumphan Wongseripipatana

2

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

Sanan Subhadhirasakul

3

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

Hiromitsu Takayama

4

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

Masaki Yokota

5

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

Koreharu Ogata

6

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

Chada Phisalaphong

7

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

Norio Aimi

8

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

Shin-ichiro Sakai

9

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

publication date

1988

3 references

16 September 2022

16 September 2022

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

volume

44

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

issue

16

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

page(s)

5075-5094

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2986012-9

cites work

Absolute configuration oOf lyngbyatoxin A (teleocidin A-1) and teleocidin A-2

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7 January 2021

Indole alkaloids isolated from Gelsemium elegans (Thailand): 19-(Z)-akuammidine, 16-epi-voacarpine, 19-hydroxydihydrogelsevirine, and the revised structure of koumidine.

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7 January 2021

Studies on the NMR spectroscopic properties of gelsemine--revisions and refinements

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7 January 2021

21-Oxogelsevirine, a New Alkaloid from Gelsemium rankinii

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7 January 2021

14 beta-Hydroxygelsedine, a new oxindole alkaloid from Gelsemium sempervirens

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7 January 2021

[Studies of plants containing Indole alkaloids. (4). Alkaloids in Ochrosia nakaiana Koidz]

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7 January 2021

Alkaloids of Tabernaemontana psychotrifolia H.B.K.

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7 January 2021

Transformation of indole alkaloids. II. On the C-D ring opening and closing reactions of indole alkaloids and the syntheses of vobasine type alkaloids (author's transl)

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7 January 2021

NMR spectra of gelsemine derivatives. The structure and biogenesis of the alkaloid gelsemine

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7 January 2021

A plausible biogenetic proposal for koumine

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7 January 2021

Rankinidine, a new indole alkaloid from Gelsemium rankinii

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7 January 2021

Indolalkaloide aus Conopharyngia durissima STAPF. 134. Mitteilung über Alkaloide [1]

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COCI

https://opencitations.net/index/api/v1/citations/10.1002/HLCA.19690520318

THE CRYSTAL STRUCTURE AND MOLECULAR ABSOLUTE CONFIGURATION OF KOUMINE HYDROBROMIDE

9 March 2024

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COCI

https://opencitations.net/index/api/v1/citations/10.7498/APS.31.547