The first chemoselective tandem acylation of the Blaise reaction intermediate: a novel method for the synthesis of α-acyl-β-enamino esters, key intermediate for pyrazoles
CASEY, M.;MOODY, CH. J.;REES, CH. W.;YOUNG, R. G., J. CHEM. SOC. PERKIN TRANS., 1985, N 4, 741-745
作者:CASEY, M.、MOODY, CH. J.、REES, CH. W.、YOUNG, R. G.
DOI:——
日期:——
The first chemoselective tandem acylation of the Blaise reaction intermediate: a novel method for the synthesis of α-acyl-β-enamino esters, key intermediate for pyrazoles
作者:Yu Sung Chun、Ki Kon Lee、Young Ok Ko、Hyunik Shin、Sang-gi Lee
DOI:10.1039/b813369g
日期:——
The Blaise reaction intermediate, a zinc bromide complex of β-enamino ester, could be activated in situ by addition of a stoichiometric or catalytic amount of n-BuLi to allow chemoselective tandem C2-acylation providing α-acyl-β-enamino esters, which are valuable intermediates for the syntheses of tri- and tetrasubstituted pyrazoles.