Preparation of fortamine and 6-epi-purpurosamine B from fortimicin B.
スポンサーリンク
概要
- 論文の詳細を見る
Benzyl alcoholysis and hydrolysis of tetrakis-<I>N</I>-(benzyloxycarbonyl)fortimicin B and further transformation of the solvolysis products are described. Several derivatives of 6-<I>epi</I>-purpurosamine B and fortamine potentially useful for the synthesis of fortimicin analogs are presented.
- 公益社団法人 日本化学会の論文
著者
-
Sano Hiroshi
Tokyo Research Laboratories Kyowa Hakko Kogyo Co. Ltd.:(present Office)shimizu Research Laboratories
-
Sakaguchi Tomoko
Tokyo Research Laboratory, Kyowa Hakko Kogyo Co., Ltd.
-
Mori Yasuki
Tokyo Research Laboratory, Kyowa Hakko
-
Sano Hiroshi
Tokyo Research Laboratory, Kyowa Hakko Kogyo Co., Ltd.
関連論文
- K-254-I(Genistein), a New Inhibitor of Ca^ and Calmodulin-Dependent Cyclic Nucleotide Phosphodiesterase from Streptosporangium vulgare(Biological Chemistry)
- Isolation and Purification of HS-142-1, a Novel Nonpeptide Antagonist for the Atrial Natriuretic Peptide Receptor, from Aureobasidium sp.(Biological Chemistry)
- K-251 Compounds, Inhibitors of Ca^ and Calmodulin-dependent Cyclic Nucleotide Phosphodiesterase from Streptoverticillium album(Biological Chemistry)
- PA157 STRUCTURE DETERMINATION OF THE NOVEL ANTHRAQUINONE ANTIBIOTICS DC92-B AND DC92-D
- Chemical transformation of seldomycin 5 into 3'-episeldomycin 5 and its antibacterial activity.
- Chemical transformation of seldomycin 5 into 3'-deoxyseldomycin 5 and related compounds.
- Preparation of fortamine and 6-epi-purpurosamine B from fortimicin B.