EFFICIENT SYNTHESIS OF BETA-AMINO-ACID AND GAMMA-AMINO-ACID DERIVATIVES USING NEW FUNCTIONALIZED ZINC REAGENTS - ENHANCED STABILITY AND REACTIVITY OF BETA-AMIDO ZINC REAGENTS IN DIMETHYLFORMAMIDE
Cs. Dexter et Rfw. Jackson, EFFICIENT SYNTHESIS OF BETA-AMINO-ACID AND GAMMA-AMINO-ACID DERIVATIVES USING NEW FUNCTIONALIZED ZINC REAGENTS - ENHANCED STABILITY AND REACTIVITY OF BETA-AMIDO ZINC REAGENTS IN DIMETHYLFORMAMIDE, Chemical communications, (1), 1998, pp. 75-76
The new zinc reagents 3 and 4 are not sufficiently stable to be prepar
ed efficiently in THF, but they can be prepared in DMF under mild and
convenient conditions; subsequent palladium-catalysed coupling with ar
omatic iodides gives protected beta- and gamma-amino acids 11 and 12 i
n generally good yields.