𝔖 Bobbio Scriptorium
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Cypridina bioluminescence III total synthesis of Cypridina luciferin

✍ Scribed by Yoshito Kishi; Toshio Goto; Shoji Inoue; Sumi Sugiura; Hisako Kishimoto


Publisher
Elsevier Science
Year
1966
Tongue
French
Weight
213 KB
Volume
7
Category
Article
ISSN
0040-4039

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✦ Synopsis


CYPRIDINA luciferin (I) has been shoosn to have the structure represented by Ia (1).

We wish to report in this oommunioation a total.


πŸ“œ SIMILAR VOLUMES


Cypridina bioluminescence I Sructure of
✍ Toshito Kishi; Toshio Goto; Yoshimasa Hirata; Osamu Shimomura; Frank H. Johnson πŸ“‚ Article πŸ“… 1966 πŸ› Elsevier Science 🌐 French βš– 421 KB

BIOLlEilNlSCENCE of Cypridina hilgendorfii (Japenese name:umi-hotaru) has been studied extensively since 1917, when Harvey (1) observed the luciferin-luciferase reaction with extracts of this animal. The luminescent system of Cypridina is one of the simplest among luminous animals and plantc 60 far

Cypridina bioluminescence VI a new route
✍ S. Inoue; S. Sugiura; H. Kakoi; T. Goto πŸ“‚ Article πŸ“… 1969 πŸ› Elsevier Science 🌐 French βš– 106 KB

A total synthesis of Cypridina luciferin (I), a bioluminescent substance obtained from Cypridina hilgendorfii (l), was achieved in 1966 (2) by reductive condensation of an appropriate 2-aminopyrazine derivative and a-keto acid, but the yield was too low to use th!s route for preparative purposes. Tw

The Structure of Cypridina Luciferin
✍ Yoshimasa Hirata; Osamu Shimomura; Shoji Eguchi πŸ“‚ Article πŸ“… 1959 πŸ› Elsevier Science 🌐 French βš– 231 KB
Biosynthesis of luciferin in the sea fir
✍ Yuichi Oba; Shin-ichi Kato; Makoto Ojika; Satoshi Inouye πŸ“‚ Article πŸ“… 2002 πŸ› Elsevier Science 🌐 French βš– 104 KB

Feeding experiment to the marine ostracod crustacean, Cypridina (Vargula) hilgendorfii, using L-tryptophan labeled with deuterium at indole ring revealed that the labeled L-tryptophan was incorporated into Cypridina luciferin as a component and the animals were able to synthesize the luciferin in a