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Colchicine is formed by para-para phenol coupling from autumnaline
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instance of
scholarly article
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title
Colchicine is formed by para-para phenol coupling from autumnaline
(English)
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main subject
(S)-(−)-colchicine
2 references
based on heuristic
inferred from title
inferred from
reverse claim
Colchicum autumnale
1 reference
inferred from
reverse claim
(S)-Autumnaline
1 reference
inferred from
reverse claim
Isoandrocymbine
1 reference
inferred from
reverse claim
author name string
Ulrich H. Maier
series ordinal
1
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Meinhart H. Zenk
series ordinal
2
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publication date
October 1997
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published in
Tetrahedron Letters
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volume
38
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page(s)
7357-7360
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issue
42
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cites work
Biosynthesis of the indole and Colchicum alkaloids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0040-4039%2897%2910011-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Incorporation of phenethylisoquinolines into colchicine in isolated seeds of Colchicum autumnale
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0040-4039%2897%2910011-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alkaloid biosynthesis. Part XVIII. Biosynthesis of colchicine from the 1-phenethylisoquinoline system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0040-4039%2897%2910011-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
444. Investigations on the biosynthesis of morphine alkaloids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0040-4039%2897%2910011-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Formation of salutaridine from (R)-reticuline by a membrane-bound cytochrome P-450 enzyme from Papaver somniferum
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0040-4039%2897%2910011-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0040-4039(97)10011-9
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