Chemical Communications 2012-09-18

Total synthesis of ascididemin via anionic cascade ring closure.

Ida Nymann Petersen, François Crestey, Jesper Langgaard Kristensen

Index: Chem. Commun. (Camb.) 48(72) , 9092-4, (2012)

Full Text: HTML

Abstract

A new and convergent synthesis of ascididemin is presented. Using an anionic cascade ring closure as the key step, this natural product is obtained in 45% overall yield in just 6 steps starting from 2'-fluoroacetophenone. This new approach was extended to the synthesis of a new isomer of ascididemin.

Related Compounds

Structure Name/CAS No. Articles
3-Bromo-4-methylpyridine Structure 3-Bromo-4-methylpyridine
CAS:3430-22-6
1-(2-Fluorophenyl)ethanone Structure 1-(2-Fluorophenyl)ethanone
CAS:445-27-2