Modular Synthesis of a Semibuckminsterfullerene

Org Lett. 2022 Jul 22;24(28):5095-5098. doi: 10.1021/acs.orglett.2c01880. Epub 2022 Jul 12.

Abstract

A convergent synthesis of dibenzochrysenes and diindenochrysenes that proceeds from difluorofluorenes and acetoxyenone 15 has been used to prepare 5,6,11,12-tetrabromosemibuckminsterfullerene (31). The synthesis is highly modular and is distinguished by proceeding through an unsymmetrical intermediate. Our work will enable the straightforward preparation of semibuckminsterfullerenes from diindenochrysenes that lack bilateral symmetry using common reagents and nonpyrolytic conditions.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Indicators and Reagents*

Substances

  • Indicators and Reagents