Reaction of secondary phosphine oxides with acylacetylenes View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2010-04

AUTHORS

M. Yu. Dvorko, T. E. Glotova, I. A. Ushakov, N. K. Gusarova

ABSTRACT

Secondary phosphine oxides reacted with 1-alkanoyl-2-phenylacetylenes in chemoselective fashion under mild conditions (20°C, THF) in the absence of a catalyst (diphenylphosphine oxide) or in the presence of potassium hydroxide [bis(2-phenylethyl)phosphine oxide] to give 1-alkyl-1-diphenyl(or 2-phenylethyl)-phosphoryl-3-phenylprop-2-yn-1-ols in up to 96% yield. The reaction of diphenylphosphine oxide with 1-alkanoyl-2-phenylacetylenes in the system KOH-THF (20°C) afforded not only adducts at the carbonyl group but also products of double α,β-addition at the triple bond, 2,3-bis(diphenylphosphoryl)-3-phenylpropan-1-ones. More... »

PAGES

485-490

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428010040056

DOI

http://dx.doi.org/10.1134/s1070428010040056

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1044998977


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