Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Synthesis of 15-Oxo- and Δ16-14β-Isobufadienolides
南原 利夫島田 和武
著者情報
ジャーナル フリー

1971 年 19 巻 1 号 p. 16-20

詳細
抄録
In order to clarify the structure-activity relationship, synthesis of the titled compounds has been undertaken. The acid-cleavage of 14α, 15α-epoxyisobufadienolide (I) followed by oxidation with chromium trioxide gave the 14β-hydroxy-15-ketone (III). The ring opening of the β-epoxide (IV) and subsequent epimerization at C-14 resulted in formation of 15-oxo-14β-isobufadienolide (VI). Upon treatment with N-bromosuccinimide and then with lithium chloride or sodium iodide 14β, 17α- and 14α, 17β-isobufadienolides (IX and XIII) were led to Δ16, Δ14, 16 and Δ16-14β, 15β-epoxy derivatives (X, XV and XVI), respectively.
著者関連情報
© The Pharmaceutical Society of Japan
前の記事 次の記事
feedback
Top