Synthetic study on antitumor antibiotic terpentecin: Construction of the carbobicyclic decalin moiety

Kenichi Takao, Susumu Kobayashi

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Carbobicyclic decalin moiety of antitumor terpentecin is prepared in a stereoselective manner from (+)-Wieland-Miescher ketone via reductive alkylation and Birch reduction.

Original languageEnglish
Pages (from-to)6685-6688
Number of pages4
JournalTetrahedron Letters
Volume38
Issue number38
DOIs
Publication statusPublished - 1997 Sep 22
Externally publishedYes

Fingerprint

Betula
Alkylation
Ketones
Anti-Bacterial Agents
terpentecin
decalin

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Synthetic study on antitumor antibiotic terpentecin : Construction of the carbobicyclic decalin moiety. / Takao, Kenichi; Kobayashi, Susumu.

In: Tetrahedron Letters, Vol. 38, No. 38, 22.09.1997, p. 6685-6688.

Research output: Contribution to journalArticle

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