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Chemical synthesis of lampteroflavin as light emitter in the luminous mushroom, lampteromyces japonicus

โœ Scribed by Hiroyuki Takahashi; Minoru Isobe; Toshio Goto


Publisher
Elsevier Science
Year
1991
Tongue
French
Weight
596 KB
Volume
47
Category
Article
ISSN
0040-4020

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โœฆ Synopsis


The synthesis of lamprerojlavin (the hght emitter of the lumrnous mushroom, Lampteromyces japonicus) is described. Protected riboflavin was stereoselecrively glycosylared wirh ribofuranosyl imidate to give largely rhe a-product Chloroethyl group which could be removed under neutral condition conrrrbured to this synthesis.

Lampteroflavin (Lf) 1 was isolated from the luminous mushroom, Lampteromyces japomcus, in 1987 by Isobe et al 1) as its bioluminescence light emitter. We are interested in the unique structure of 1 among


๐Ÿ“œ SIMILAR VOLUMES


Lampteroflavin, the first riboflavinyl a
โœ Duangchan Uyakul; Minoru Isobe; Toshio Goto ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 869 KB

## Lampteroflavin (1, Lf) was isolated from the suspension of alive gills of the luminous mushroom, Lampteromycea japonicus. It was hydrolyzed into riboflavin (2, Rf) and D-riboee, which were identified by means of HE&C, NMR, CD and FAB-MS/MS. The structure was concluded to be 5'-riboflavinyl a-