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Direct C-H arylation and alkenylation of 1-substituted tetrazoles: phosphine as stabilizing factor

M. Spulak, R. Lubojacky, P. Senel, J. Kunes, M. Pour

Jazyk angličtina Země Spojené státy americké

Typ dokumentu práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc12008675

Direct arylation and alkenylation of 1-substituted tetrazoles was achieved via Pd catalysis in the presence of CuI and Cs(2)CO(3). Unlike the related reactions of imidazoles and purines, phosphine ligand was necessary to prevent the intermediate tetrazolyl-Pd(II) species from fragmentation into the corresponding cyanamide. Various 1,5-disubstituted tetrazoles were prepared with good to excellent isolated yields.

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$a Špulák, Marcel. $7 xx0248693 $u Centre for New Antivirals and Antineoplastics, Department of Inorganic and Organic Chemistry, Charles University in Prague, Faculty of Pharmacy in Hradec Kralove, CZ-500 03 Hradec Kralove, Czech Republic.
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$a Direct C-H arylation and alkenylation of 1-substituted tetrazoles: phosphine as stabilizing factor $c M. Spulak, R. Lubojacky, P. Senel, J. Kunes, M. Pour
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$a Direct arylation and alkenylation of 1-substituted tetrazoles was achieved via Pd catalysis in the presence of CuI and Cs(2)CO(3). Unlike the related reactions of imidazoles and purines, phosphine ligand was necessary to prevent the intermediate tetrazolyl-Pd(II) species from fragmentation into the corresponding cyanamide. Various 1,5-disubstituted tetrazoles were prepared with good to excellent isolated yields.
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