Iodosulfonylation of [1.1.1]Propellane

Abstract

An efficient disubstituted functionalization of [1.1.1]propellane has been developed. The protocol utilizes sulfonyl hydrazides and N-iodosuccinimide, enabling the introduction of iodine and sulfonyl groups into bicyclo[1.1.1]pentane (BCP) in moderate to excellent yields. It has the advantages of simple operation, mild conditions, and broad substrate scope.

Key words

[1.1.1]propellane - bicyclo[1.1.1]pentane - sulfonyl hydrazides - iodosulfonylation - radical reaction

• References

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