Title of article :
Chemistry of renieramycins. Part 6: Transformation of renieramycin M into jorumycin and renieramycin J including oxidative degradation products, mimosamycin, renierone, and renierol acetate
Author/Authors :
Naoki Saito، نويسنده , , Chieko Tanaka، نويسنده , , Yu-ichi Koizumi، نويسنده , , Khanit Suwanborirux، نويسنده , , Surattana Amnuoypol، نويسنده , , Sunibhond Pummangura، نويسنده , , Akinori Kubo، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2004
Abstract :
The transformation of renieramycin M () into renieramycin J () and jorumycin () is presented along with the results of antiproliferative assay data. The chemical stability and the oxidative degradation of and renieramycin E () to generate simple isoquinoline alkaloids, such as mimosamycin (), renierol acetate (), and renierone () are also described.
Keywords :
Renieramycin M , Jorumycin , Transformation , Antitumor activity , Oxidative degradation
Journal title :
Tetrahedron
Journal title :
Tetrahedron