Kabes, Connor Q.’s team published research in Synthesis in 2020 | CAS: 2418-95-3

H-Lys(Boc)-OH(cas: 2418-95-3) belongs to amino acids. These amino acids may be present in low concentrations and play a vital part as an intermediate in a biosynthetic pathway, e.g., ornithine, homoserine, or cystathionine. In contrast they may act as a major storage form of nitrogen, e.g., canavanine in the seed of Canavalia ensiformis, or may be formed in high amounts in response to an external stress, e.g., γ-aminobutyrate.Related Products of 2418-95-3 It is possible that some of these nonprotein amino acids may serve as insecticidal or fungicidal agents.

Related Products of 2418-95-3On November 30, 2020 ,《Syntheses of enantiopure 1,2-ethylenediamines with tethered secondary amines of the formula H2NCH2CH[(CH2)nNHMe]NH2 (n = 1 – 4) from α-amino acids: New agents for asymmetric catalysis》 appeared in Synthesis. The author of the article were Kabes, Connor Q.; Gunn, Jack H.; Selbst, Maximilian A.; Lucas, Reagan F.; Gladysz, John A.. The article conveys some information:

Tris(hydrochloride) adducts of the title compounds are prepared from the inexpensive α-amino acids H2N(C:O)CH2CH(NH2)CO2H, HO(C:O)(CH2)nCH(NH 2)CO 2H (n = 1, 2), and H2N(CH2)4CH(NH2)CO2H, resp. (steps/overall yield = 5/32%, 7/30%, 7/33%, 5/38%). The NH2 group that is remote from the secondary amine is installed via BH3 reduction of an amide [(C=O)NR2] derived from an α-amino carboxylic acid. The MeNHCH2 units are introduced by BH3 reductions of alkyl carbamate [RO(C:O)NHCH2; R = Et, t-Bu] or amide [MeHN(C:O)] moieties. In the experiment, the researchers used many compounds, for example, H-Lys(Boc)-OH(cas: 2418-95-3Related Products of 2418-95-3)

H-Lys(Boc)-OH(cas: 2418-95-3) belongs to amino acids. These amino acids may be present in low concentrations and play a vital part as an intermediate in a biosynthetic pathway, e.g., ornithine, homoserine, or cystathionine. In contrast they may act as a major storage form of nitrogen, e.g., canavanine in the seed of Canavalia ensiformis, or may be formed in high amounts in response to an external stress, e.g., γ-aminobutyrate.Related Products of 2418-95-3 It is possible that some of these nonprotein amino acids may serve as insecticidal or fungicidal agents.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics