Oppenauer-type synthesis of &amp;alpha;, &amp;beta;-acetylenic ketones from tetra(phenylethynyl)tin and aromatic aldehydes

Levashov, A. S.; Buriy, Dmitriy; Коншин, В. В.; Dotsenko, V. V.; Аксенова, И. В.; Аксенов, Н. А.

doi:10.3390/ecsoc-21-04807

Proceedings of the 21st International Electronic Conference on Synthetic Organic Chemistry 2017

DOI: 10.3390/ecsoc-21-04807

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Oppenauer-type synthesis of α, β-acetylenic ketones from tetra(phenylethynyl)tin and aromatic aldehydes

A. S. Levashov

Dmitriy Buriy

В. В. Коншин

et al.

Abstract: Tetra(phenylethynyl)tin reacts with aromatic aldehydes in the presence of a Lewis acid followed by the Oppenauer-type in situ oxidation of propargyl alcohols to give acetylenic ketones in a very good yield.

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Oppenauer-type synthesis of α, β-acetylenic ketones from tetra(phenylethynyl)tin and aromatic aldehydes

Abstract: Tetra(phenylethynyl)tin reacts with aromatic aldehydes in the presence of a Lewis acid followed by the Oppenauer-type in situ oxidation of propargyl alcohols to give acetylenic ketones in a very good yield.

Cited by 0 publications

References 16 publications

No citations

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