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CIDNP as a tool to unveil the reaction mechanism: interaction of mixed phosphonium-iodonium ylide with p-methoxyphenylacetylene.


ABSTRACT: In situ acquisition of the reaction between benzoyl phosphonium-iodonium ylide and p-methoxyphenylacetylene in an NMR spectrometer reveals the CIDNP effect in 31P and 1H NMR spectra of major products, substituted furan (emission) and phosphonium salt (enhanced absorption). The mechanism of products formation via radical pairs is discussed.

SUBMITTER: Levina II 

PROVIDER: S-EPMC9070124 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

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CIDNP as a tool to unveil the reaction mechanism: interaction of mixed phosphonium-iodonium ylide with <i>p</i>-methoxyphenylacetylene.

Levina Irina I II   Tarasov Valery F VF   Podrugina Tatyana A TA   Nekipelova Tatiana D TD  

RSC advances 20190821 45


<i>In situ</i> acquisition of the reaction between benzoyl phosphonium-iodonium ylide and <i>p</i>-methoxyphenylacetylene in an NMR spectrometer reveals the CIDNP effect in <sup>31</sup>P and <sup>1</sup>H NMR spectra of major products, substituted furan (emission) and phosphonium salt (enhanced absorption). The mechanism of products formation <i>via</i> radical pairs is discussed. ...[more]

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