Synthéses de β-et δ-aryl α-amino esters: réactions d'anions benzyliques chrome tricarbonyle sur des halogéno α-amino esters
摘要:
Methyl arylacetate-tricarbonylchromium complexes are readily alkylated by halogeno alpha-amino esters in the presence of NaH or (t)BuOK to give, after decomplexation, beta- and delta-aryl amino esters in good yields.
JENHI, A.;LAVERGNE, J. -P.;VIALLEFONT, PH., J. ORGANOMET. CHEM., 401,(1991) N-2, C14-C16
作者:JENHI, A.、LAVERGNE, J. -P.、VIALLEFONT, PH.
DOI:——
日期:——
Synthéses de β-et δ-aryl α-amino esters: réactions d'anions benzyliques chrome tricarbonyle sur des halogéno α-amino esters
作者:A. Jenhi、J.-P. Lavergne、Ph. Viallefont
DOI:10.1016/0022-328x(91)86214-b
日期:1991.1
Methyl arylacetate-tricarbonylchromium complexes are readily alkylated by halogeno alpha-amino esters in the presence of NaH or (t)BuOK to give, after decomplexation, beta- and delta-aryl amino esters in good yields.