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1.
J Org Chem ; 87(23): 15820-15829, 2022 12 02.
Artículo en Inglés | MEDLINE | ID: mdl-36374155

RESUMEN

An efficient copper-catalyzed radical hydrazono-phosphorylation of alkenes with hydrazine derivatives and diarylphosphine oxides is described. The reaction provides a general and convenient method toward the synthesis of diverse ß-hydrazonophosphine oxides in satisfactory yields. Based on conducted mechanistic experiments, a mechanism involving Ag-catalyzed oxidative generation of phosphinoyl radicals and subsequent addition to alkenes followed by Cu-assisted hydrazonation is proposed. Moreover, the practicability of the reaction is successfully demonstrated by its successful application on a gram scale.


Asunto(s)
Alquenos , Cobre , Catálisis , Oxidación-Reducción , Óxidos
2.
J Org Chem ; 87(21): 14555-14564, 2022 Nov 04.
Artículo en Inglés | MEDLINE | ID: mdl-36264682

RESUMEN

A copper-catalyzed stereoselective phosphono-hydrazonation of terminal alkynes with alkyl carbazates and diarylphosphine oxides is described. This methodology provides facile access to a variety of ß-hydrazonophosphine oxides in satisfactory yields. The reaction proceeds under mild conditions and exhibits good functional group tolerance. A mechanism featuring persulfate-mediated oxidative generation of phosphinoyl radicals and copper-assisted hydrazonation is proposed.

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