KINAMYCIN BIOSYNTHESIS - SYNTHESIS, ISOLATION, AND INCORPORATION OF STEALTHIN-C, AN AMINOBENZO[B]FLUORENE

Citation
Sj. Gould et al., KINAMYCIN BIOSYNTHESIS - SYNTHESIS, ISOLATION, AND INCORPORATION OF STEALTHIN-C, AN AMINOBENZO[B]FLUORENE, Journal of organic chemistry, 62(2), 1997, pp. 320-324
Citations number
31
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
00223263
Volume
62
Issue
2
Year of publication
1997
Pages
320 - 324
Database
ISI
SICI code
0022-3263(1997)62:2<320:KB-SIA>2.0.ZU;2-B
Abstract
A new intermediate in the biosynthesis of the benzo[b]fluorene antibio tic, kinamycin D, has been identified. 5,9-trihydroxy-2-methyl-10H-ben zo[b]fluoren-10-one was synthesized and shown to be present in extract s of treptomyces murayamaensis fermentations. A deuterated sample was prepared and shown to be specifically incorporated into kinamycin D. T his new intermediate, now named stealthin C, is also the probable hydr oxylation substrate for the biosynthesis of stealthin A by S. Viridoch romogenes.