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
Pages
9
From page
3873
To page
3881
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
Serial Year
2004
Journal title
Tetrahedron
Record number
1085399
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