Title of article :
Facile conversion of Biginelli 3,4-dihydropyrimidin-2(1H)-thiones to 2-(2-hydroxy-2-arylvinyl) dihydropyrimidines via Eschenmoser coupling
Author/Authors :
Singh، نويسنده , , Sukhdeep and Schober، نويسنده , , Andreas and Gebinoga، نويسنده , , Michael and Alexander Groك، نويسنده , , G.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2009
Abstract :
A one-pot, two-step synthesis protocol for the conversion of Biginelli 3,4-dihydropyrimidin-2(1H)-thiones to 2-(2-hydroxy-2-arylvinyl) dihydropyrimidine (DHPM) derivatives via Eschenmoser sulfide contraction coupling is described. Solution phase as well as solid-supported protocol was carried out for the decoration of the Biginelli DHMP scaffold at the C-2 position. The scope of the optimized protocol is demonstrated for different DHMP precursors.
Keywords :
Eschenmoser , Sulfide contraction , Eschenmoser coupling , Polymer supported , DHPM , Biginelli , Drug research , Privileged structure , Triphenylphosphine
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters