- 询价
- ITI Biochem
- 美国
- 1161-13-1
- 2025年07月19日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
详询
- 保质期：
详询
- 英文名：
N-CBZ-L-phenylalanine
- 库存：
98
- 供应商：
北京孚博
- CAS号：
1161-13-1
- 规格：
1g
CAS：1161-13-1
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文献和实验CarbonCarbon Bond-Forming Enzymes for the Synthesis of Non-natural Amino Acids
An enzymatic methodology for the preparation of β-hydroxy-α-amino acid derivatives is described. The method consists of the stereoselective aldol addition reaction of glycine to N -Cbz-amino aldehydes furnishing 3-hydroxy-2,4-diaminobutyric
Synthesis of Cbz-Protected Ketomethylene Dipeptide Isosteres
1 are chemically characterized by a 1,4-disposition of the carbonyl groups (ketone and carboxylate) and have an alkyl group at C-2 that is a chiral center. Protecting groups at amino nitrogen (typically carbamate such as Cbz or Boc) and the carboxyl group
Methylated Polyamines as Research Tools
resulted in corresponding di-Boc-amines, which after deprotection gave target β- and γ-MeSpd’s. To prepare α-MeSpd, the starting compound, 3-amino-1-butanol, was converted into N -Cbz-3-amino-1-butyl methanesulfonate, which alkylated putrescine
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