
Tetrahedron Letters p. 5801 - 5804 (1991)
Update date:2022-08-11
Topics:
Kakinuma, Katsumi
Koudate, Takashi
Li, Hui-Ying
Eguchi, Tadashi
A divergent and highly enantioselective synthetic methodology not only for both enantiomers of α-amino acids but for both chirally deuterated glycines from a single starting material was developed by making use of stereocontrol with antiparallel double repulsion on the diacetone-D-glucos-3-ulose template.
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