摘要

A concise synthesis of denbinobin is described via an intramolecular free radical cyclization and Fremy's salt mediated oxidation as a key reactions. A seven-step process starting from commercially available 3,5-dimethoxybenzyl bromide (6) and 2-bromoisovanillin (5) effectively constructs the natural product denbinobin (1).

原文英語
頁(從 - 到)8103-8104
頁數2
期刊Tetrahedron Letters
46
發行號47
DOIs
出版狀態已發佈 - 十一月 21 2005

ASJC Scopus subject areas

  • 生物化學
  • 藥物發現
  • 有機化學

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