(Q104915209)

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2984121-7

main subject

Thermopsis lupinoides

1 reference

inferred from

reverse claim

Thermopsis lanceolata

1 reference

inferred from

reverse claim

(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one

1 reference

inferred from

reverse claim

(1S,9R,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one

1 reference

1 reference

(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one

1 reference

1 reference

(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane-6,16-dione

1 reference

1 reference

(1R,2R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one

1 reference

1 reference

Shigeru Ohmiya

1

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2984121-7

Hirotaka Otomasu

series ordinal

2

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2984121-7

Joju Haginiwa

series ordinal

3

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2984121-7

Isamu Murakoshi

series ordinal

4

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2984121-7

publication date

January 1984

3 references

16 September 2022

16 September 2022

3

1 reference

inferred from page(s)

published in

Phytochemistry

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2984121-7

volume

23

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2984121-7

page(s)

2665-2667

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2984121-7

issue

11

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2984121-7

cites work

N-Formylcytisine: A new alkaloid from Thermopsis chinensis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021

(+)-5α,9α-dihydroxymatrine, a new lupin alkaloid from Euchresta horsfeldii

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021

(−)-(Trans-4′-β-d-glycopyranosyloxy-3′-methoxycinnamyl)-lupinine, a new lupin alkaloid in Lupinus seedlings

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021

The alkaloid constituents of Euchresta japonica and the stereochemical assignment of two isomeric sophoridine N-oxides.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021

(−)-Epilamprolobine and its N-oxide, lupin alkaloids from Sophora tomentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021

Two cage-type lupin alkaloids from Sophora franchetiana

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021

Lupin alkaloids from Sophora mollis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021

Lupin alkaloids from Echinosophora koreensis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021

Isokuraramine and (−)-7,11-dehydromatrine, lupin alkaloids from flowers of Sophora flavescens

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021

STUDIES ON LUPIN ALKALOIDS. II. ABSOLUTE CONFIGURATION OF LUPIN ALKALOID. I

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021

STUDIES ON LUPIN ALKALOIDS. 3. ABSOLUTE CONFIGURATIONS OF LUPIN ALKALOIDS. II

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2984121-7

7 January 2021