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Copper tetrakis acetonitrile>, hexafluorophosphate

Similarly, the nitrene transfer reaction from 128 is facilitated by a variety of catalysts, including MTO (136) <01JCS(CC)235>, the lri(pyrazolyl)borate-coppcr(l) complex 137 <01OL1423>, and tetrakis(acetonitrile)copper(I) hexafluorophosphate (138) <01JA7707>. In the latter case, the reaction can be carried out using a sulfonamide and the primary oxidant, iodosylbenzene, whereby the actual nitrene transfer reagent 128 is presumed to be formed in situ. In all cases, acetonitrile appears to be the solvent of choice. [Pg.67]

Soleimani, E. Khodaei, M. M. Batooie, N. Samadi, S. Tetrakis(acetonitrile)copper(I) hexafluorophosphate catalyzed coumarin synthesis via Pechmann condensation under solvent-free condition. J. Heterocycl. Chem. 2012, 49, 409-412. [Pg.55]


See other pages where Copper tetrakis acetonitrile>, hexafluorophosphate is mentioned: [Pg.405]    [Pg.90]    [Pg.91]    [Pg.56]    [Pg.411]    [Pg.683]    [Pg.748]    [Pg.683]    [Pg.748]    [Pg.68]    [Pg.168]    [Pg.637]    [Pg.617]    [Pg.69]    [Pg.15]    [Pg.44]   
See also in sourсe #XX -- [ Pg.19 , Pg.90 ]




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Acetonitrile copper

Copper hexafluorophosphate

Copper tetrakis

Hexafluorophosphate

Hexafluorophosphates

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