Enantioselective Synthesis of the C11-C24 Segment of Macrolactin a via Organoiron Methodology
The enantioselective synthesis of the Fe(CO)3 completed C11-C24 segment of macrolactin A has been accomplished from rac-(methyl 6-oxo-2,4-hexadienoate)Fe(CO)3 in 11 steps (>50% ee).
Prahlad, Vadapalli and Donaldson, William, "Enantioselective Synthesis of the C11-C24 Segment of Macrolactin a via Organoiron Methodology" (1996). Chemistry Faculty Research and Publications. 841.