Ra. August et al., STEREOSPECIFIC SYNTHESIS OF (2S,4R)-[5,5,5-H-2(3)]LEUCINE, Journal of the Chemical Society. Perkin transactions. I, (6), 1996, pp. 507-514
The first stereospecific chemical synthesis of a sample of the amino a
cid (2S)-leucine labelled in one of the diastereotopic methyl groups h
as been achieved using (2S)-pyroglutamic acid as a chiral template, Th
is has been used to develop a method for assigning resonances to the d
iastereotopic methyl groups of the leucine residues in the H-1 NMR spe
ctra of proteins.