Work

Diterpenoids. XVI. Reduction of 6β-Hydroxy-enantio-podocarpa-8, 11, 13-trien-16-oic Acid Derivative

Year: 1971

Type: article

Abstract: Synthesis of 6β-hydroxy (acetoxy)-enantio-podocarpan-oic acid type compounds (e.g. V, VII ; XIV, XVI and XV, XVIII) were herein accomplished. These compounds are regarded as starting materials for examination of a notable epimerization at a lactonization. Furthermore, it is interesting that they have basic skeleton of many natural diterpenoids having C6-oxygen function.

Source: Chemical and Pharmaceutical Bulletin

DOI: 10.1248/cpb.19.1756

Authors: AKIRA TAHARA, YASUO OHTSUKA, NORIHIDE UMINO, KAZUO NAGASAWA, KENICHI HIRAO

Language: English

Topic: Bioactive Natural Diterpenoids Research

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

Open Access status: bronze

OpenAlex ID: W1488174331

FWCI: 0.708

Cites:

Cited by: 1

Related to: 10