Fehrentz, Jean-Alain published the artcileSynthesis of chiral N-protected α-amino aldehydes by reduction of N-protected N-carboxyanhydrides (UNCAs), Name: (R)-tert-Butyl (3-methyl-1-oxobutan-2-yl)carbamate, the publication is Tetrahedron Letters (1994), 35(48), 9031-4, database is CAplus.
Pure N-protected (Boc, Z, Fmoc) α-amino aldehydes were obtained in high yields by reduction of N-protected N-carboxyanhydrides with equivalent amounts of LiAlH(OCMe3)3 or lithium tris[(3-ethyl-3-pentyl)oxy]aluminum hydride (LTEPA) in THF as solvent. The reaction is simple, rapid and proceeds without detectable racemization.
Tetrahedron Letters published new progress about 106391-88-2. 106391-88-2 belongs to esters-buliding-blocks, auxiliary class Amine,Aliphatic hydrocarbon chain,Amide,Aldehyde, name is (R)-tert-Butyl (3-methyl-1-oxobutan-2-yl)carbamate, and the molecular formula is C10H19NO3, Name: (R)-tert-Butyl (3-methyl-1-oxobutan-2-yl)carbamate.
Referemce:
https://en.wikipedia.org/wiki/Ester,
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