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Synthesis of ethynylphosphonate esters. A novel organosilicon rearrangement
Journal of the Chemical Society C: Organic Pub Date : , DOI:10.1039/J39690002273
Abstract

The synthesis of ethynylphosphonate esters in high yield is described. Di-isopropyl trimethylsilylethynylphosphonate, an intermediate in the synthesis of the di-isopropyl ester, undergoes a novel thermal rearrangement with loss of propene and migration of silicon from carbon to oxygen.

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