The Schmidt rearrangement using trimethylsilyl azide with various α-dialkylated β-keto esters affords a convenientsynthesis of tetrazole, precursors of α-dialkylated α-amino acids.
Freylon, Annales de Chimie (Cachan, France), 1910, vol. <8>19, p. 566
作者:Freylon
DOI:——
日期:——
264. α-Methylenic reactivity in olefinic systems. Part IV. The structure of the dimeride formed by the stannic chloride-catalysed polymerisation of trimethylethylene. Synthesis and characterisation of isomeric methyl hexyl ketones