CHIRAL AMINAL TEMPLATES - DIASTEREOSELECTIVE ADDITION TO HYDRAZONES -AN ASYMMETRIC-SYNTHESIS OF ALPHA-AMINO ALDEHYDES

The monohydrazone of glyoxal may be derivatized into a chiral aminal w ith diamine 7. The resulting chiral reagent 13 reacts with complete di astereocontrol with organolithium reagents in THE This sterically cont rolled reaction may be altered to chelation control by using Grignard reagents in toluene, affording the opposite diastereomer in excellent de. The N-N bond of the hydrazine functionality is then cleaved with R aney nickel, assisted by ultrasound. After protection of the resulting primary amino functionality, the aminal is hydrolyzed to afford the d esired alpha-amino aldehydes without epimerization. The same reaction sequence, without cleavage of the N-N bond, affords an alpha-hydrazino aldehyde.