EMAIL THIS PAGE TO A FRIEND

The Journal of organic chemistry

Synthesis of the scalarane sesterterpenoid 16-deacetoxy-12-epi-scalarafuranacetate.


PMID 21800844

Abstract

The marine natural product 16-deacetoxy-12-epi-scalarafuranacetate, isolated from Spongua officinalis , was synthesized in 18 linear steps, starting from (-)-sclareol, with high stereoselectivity and an overall yield of 6.1%. The intermediate 16-deacetoxy-12-epi-scalarafuran could be easily transformed into a series of natural scalarane sesterterpenoids in a few steps.

Related Materials

Product #

Image

Description

Molecular Formula

Add to Cart

357995
Sclareol, 98%
C20H36O2