Intramolecular Rhodium Catalyzed Sigmatropic Rearrangement of Diazo-Derived Oxo-nium and Sulfonium Ylides: A Versatile Approach for the Synthesis of Functionalized Chromenes and Thiochromenes

14 March 2025, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Dirhodium(II)-catalyzed regio-divergent intramolecular rearrangement of oxonium and sulfonium ylides, generated from diazo arylidene succinimides (DAS), has been achieved at room temperature. Allyloxy and thioallyl-substituted DAS deriva-tives were strategically designed and synthesized to explore their reactivity in these rearrangements. The transformations are proposed to proceed via oxonium or sulfur ylide intermediates, followed by [1,2]- or [1,4]-sigmatropic shifts, leading to chromene and thiochromene frameworks. This strategy employs mild reaction conditions and represents the first applica-tion of sigmatropic rearrangement for the construction of bioactive chromene and thiochromene scaffolds.

Keywords

Rhodium catalysis
Sigmatropic Rearrangement
Chromenes
Thiochromenes

Supplementary materials

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Title
Intramolecular Rhodium Catalyzed Sigmatropic Rearrangement of Diazo-Derived Oxo-nium and Sulfonium Ylides: A Versatile Approach for the Synthesis of Functionalized Chromenes and Thiochromenes
Description
The Supporting information provides detailed experimental procedure, analytical data, copies of 1H, 13C{1H}, F19 Spectra NMR spectra.
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