(Q104914010)

http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900545-3

main subject

Selaginella delicatula

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5-[(6,8-dimethyl-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-4-yl)methyl]-1,7-dimethyl-3,4,6,7,8,8a-hexahydro-2H-quinoline

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1-[(7S,8aS)-5-[[(4S,6R,8R,9aS)-6,8-dimethyl-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-4-yl]methyl]-7-methyl-3,4,6,7,8,8a-hexahydro-2H-quinolin-1-yl]ethanone

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(7S,8aS)-5-[[(4S,6R,8R,9aS)-6,8-dimethyl-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-4-yl]methyl]-7-methyl-1,2,3,4,6,7,8,8a-octahydroquinoline

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Yusuke Hirasawa

1

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900545-3

Hiroshi Morita

series ordinal

2

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900545-3

Jun'ichi Kobayashi

series ordinal

3

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900545-3

publication date

May 2003

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16 September 2022

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900545-3

volume

59

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900545-3

issue

20

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900545-3

page(s)

3567-3573

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2803%2900545-3

cites work

The lycopodium alkaloids

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https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

Biosynthesis of lycopodine: incorporation of acetate via an intermediate with C2v symmetry

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https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

The structures of huperzine A and B, two new alkaloids exhibiting marked anticholinesterase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

A short synthesis of (+/-)-13-deoxyserratine

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https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

First total synthesis of Lycopodium alkaloids of the magellanane group. Enantioselective total syntheses of (-)-magellanine and (+)-magellaninone

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https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

Serratezomines A--C, new alkaloids from Lycopodium serratum var. serratum

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https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

Complanadine A, a new dimeric alkaloid from Lycopodium complanatum

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

Lyconadin A, a novel alkaloid from Lycopodium complanatum

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

Lyconesidines A–C, new alkaloids from Lycopodium chinense

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https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

Senepodine A, a novel C22N2 alkaloid from Lycopodium chinense

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

A biomimetic transformation of serratinine into serratezomine A through a modified Polonovski reaction

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

LYCOPODIUM ALKALOIDS: VII. LYCODOLINE (ALKALOID L.8)

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https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

A new type of Lycopodium alkaloid. The C30N3 alkaloids from Lycopodium lucidulum

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https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

Structure of oxolucidine A, a lycopodium alkaloid

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021

Four alkaloids, lucidine B, oxolucidine A, lucidine A, and lucidulinone from Lycopodium lucidulum

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900545-3

7 January 2021