Johnson, Erik P. published the artcilePreparation of α-hydroxy-β-Fmoc amino acids from N-Boc amino acids, Safety of (R)-tert-Butyl (3-methyl-1-oxobutan-2-yl)carbamate, the publication is Synthesis (2011), 4023-4026, database is CAplus.
A general method for the conversion of N-Boc (Boc = tert-butoxycarbonyl) amino acids into their homologated α-hydroxy-β-Fmoc (Fmoc = 9-fluorenylmethoxycarbonyl) amino acids is described. The protocol involved preparation of the amino aldehyde by reduction of the corresponding Weinreb amides, hydrocyanation, and hydrolysis of the nitrile group, followed by reprotection of the amino acid as the Fmoc derivative
Synthesis 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, Safety of (R)-tert-Butyl (3-methyl-1-oxobutan-2-yl)carbamate.
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