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pro vyhledávání: '"Touru Ibaragi"'
Publikováno v:
Tetrahedron. 56:1463-1468
A method for the preparation of α-azido-masked acyl cyanides as synthetic equivalents of N-protected–C-activated α-amino acids was developed using carbon–carbon bond formation between aldehydes and the Masked Acyl Cyanide Reagents, followed by
Publikováno v:
Tetrahedron Letters. 40:1319-1322
A highly stereoselective synthesis of an alkenylated malonic diamide starting from a γ,δ-epoxy-α,β-unsaturated carboxamide was accomplished using the masked acyl cyanide (MAC: the protected hydroxymalonitrile) via palladium-catalyzed regio- and s
Publikováno v:
ChemInform. 30
A highly stereoselective synthesis of an alkenylated malonic diamide starting from a γ,δ-epoxy-α,β-unsaturated carboxamide was accomplished using the masked acyl cyanide (MAC: the protected hydroxymalonitrile) via palladium-catalyzed regio- and s
Publikováno v:
ChemInform. 31
A method for the preparation of α-azido-masked acyl cyanides as synthetic equivalents of N-protected–C-activated α-amino acids was developed using carbon–carbon bond formation between aldehydes and the Masked Acyl Cyanide Reagents, followed by