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Lactoyl-CoA 全氟丁基戊烷白叶藤碱全氟己基辛烷新白叶藤碱壳寡糖特色专题-生物多肽

2584-75-0 (DL-Β-苯基丝氨酸苏式,DL-BETA-PHENYLSERINE THREO FORM)

结构式：

DL-Β-苯基丝氨酸苏式结构式图片|2584-75-0结构式图片

DL-Β-苯基丝氨酸苏式MOL文件

CAS号：

2584-75-0

中文名称：

DL-Β-苯基丝氨酸苏式

英文名称：

DL-BETA-PHENYLSERINE THREO FORM

分子式：

C₉H₁₁NO₃

分子量：

181.19

DL-Β-苯基丝氨酸苏式(2584-75-0)名称与标识符

名称

中文别名：

DL-Β-苯基丝氨酸苏式;

英文别名：

DL-BETA-PHENYLSERINE THREO FORM;threoform;DL-3-PHENYLSERINE;DL-BETA-PHENYLSERINE;dl-threo-B-phenylserine;2-AMINO-3-HYDROXY-3-PHENYLPROPIONIC ACID;2-AMINO-3-HYDROXY-3-PHENYLPROPANOIC ACID THREO FORM;(.+-.)-N-CBZ-3-phenylisoserine ethyl ester;(2RS,3SR)-2-amino-3-hydroxy-3-phenylpropanoic acid;AG-B-35921;AK119100;CTK7F8350;KB-206613;N-benzoyl-(2R*,3S*)-3-phenylisoserine;N-BENZOYL-(2S,3R)-3-AMINO-2-HYDROXY-3-PHENYL-PROPANOIC ACID;N-Benzoyl-(2S,3R)-3-amino-2-hydroxy-3-phenyl-propionic acid;rac-threo-phenylserine;threo N-benzoyl-3-phenylisoserine;

DL-Β-苯基丝氨酸苏式(2584-75-0)物化性质

实验特性

LogP : 0.83220
PSA : 83.55000

DL-Β-苯基丝氨酸苏式(2584-75-0)相关文献

1. Tetramate derivatives by chemoselective Dieckmann ring closure of allo-phenylserines, and their antibacterial activity
Liban Saney,Kirsten E. Christensen,Miroslav Genov,Alexander Pretsch,Dagmar Pretsch,Mark G. Moloney Org. Biomol. Chem. 2023 21 4061
2. A new d-threonine aldolase as a promising biocatalyst for highly stereoselective preparation of chiral aromatic β-hydroxy-α-amino acids
Qijia Chen,Xi Chen,Yunfeng Cui,Jie Ren,Wei Lu,Jinhui Feng,Qiaqing Wu,Dunming Zhu Catal. Sci. Technol. 2017 7 5964
3. Characteristics of l-threonine transaldolase for asymmetric synthesis of β-hydroxy-α-amino acids
Lian Xu,Li-Chao Wang,Xin-Qi Xu,Juan Lin Catal. Sci. Technol. 2019 9 5943
4. Synthesis of fused tetramate-oxazolidine and -imidazolidine derivatives and their antibacterial activity
Liban Saney,Tharindi Panduwawala,Xiang Li,Kirsten E. Christensen,Miroslav Genov,Alexander Pretsch,Dagmar Pretsch,Mark G. Moloney Org. Biomol. Chem. 2023 21 4801
5. In-peptide synthesis of di-oxazolidinone and dehydroamino acid–oxazolidinone motifs as β-turn inducers
Rossella De Marco,Arianna Greco,Sebastiano Rupiani,Alessandra Tolomelli,Claudia Tomasini,Silvia Pieraccini,Luca Gentilucci Org. Biomol. Chem. 2013 11 4316
6. 56. Some derivatives of β-phenylserine
D. O. Holland,P. A. Jenkins,J. H. C. Nayler J. Chem. Soc. 1953 273
7. Formation of an aminoacyl-S-enzyme intermediate is a key step in the biosynthesis of chloramphenicol
Michelle Pacholec,Jason K. Sello,Christopher T. Walsh,Michael G. Thomas Org. Biomol. Chem. 2007 5 1692
8. Synthesis of a silicon-containing analogue of chloramphenicol
Max Frankel,Mordechai Broze,David Gertner,Albert Zilkha J. Chem. Soc. C 1966 249
9. The β-phenylserine series. Part III
Ernst D. Bergmann,H. Bendas,E. Krakauer J. Chem. Soc. 1954 1064
10. 329. The β-phenylserine series. Part IV
Ernst D. Bergmann,H. Resnick J. Chem. Soc. 1956 1662

目录

相关化合物

7352-06-9(（2R，3R）-2-氨基-3-羟基-3-苯丙酸) 207605-47-8(DL-3-苯基丝氨酸水合物) 313222-82-1(D-3-苯基丝氨酸一水物) 109120-55-0((2R,3S)-3-苯基丝氨酸) 79002-32-7(2-氨基-2-(苯并呋喃-5-基)乙酰胺) 790254-33-0(1-(2,2,2-Trifluoroethyl)-1H-pyrazole-4-carbaldehyde) 791098-21-0(Methyl 4-iodo-2-nitrobenzoate) 78406-90-3((2-BROMOPHENETHYL)GUANIDINE)

问答

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