Organic & biomolecular chemistry

ω-Transaminase-catalyzed asymmetric synthesis of unnatural amino acids using isopropylamine as an amino donor

ES Park, JY Dong, JS Shin

Index: Organic and Biomolecular Chemistry, , vol. 11, # 40 p. 6929 - 6933

Full Text: HTML

Citation Number: 23

Abstract

... Chem., 2013, 11, 6929-6933 Show Compounds Show Chemical Terms. ... A number of chemocatalytic 7–10 and biocatalytic 2,3,11 methods have been developed to enable cost-effective ... PLP and 5 U mL −1 OATA in 50 mM phosphate buffer (pH 7). The reaction volume ...

Related Articles:

Catalytic Hydrogenation of Chiral α??Amino and α??Hydroxy Esters at Room Temperature with Nishimura Catalyst without Racemization

[Advanced Synthesis and Catalysis, , vol. 343, # 8 p. 802 - 808]

Simple conversion of fully protected amino acids to zwitterions

[Tetrahedron Letters, , vol. 53, # 12 p. 1433 - 1434]

Microbial Conversion of dl-5-Substituted Hydantoins to the Corresponding l5-Amino Acids by Bacillus stearothermophilus NS1122A

[Bioscience, Biotechnology and Biochemistry, , vol. 58, # 2 p. 265 - 270]

A novel type of PdMC-catalyzed hydrogenation using a catalyst poison: Chemoselective inhibition of the hydrogenolysis for O-benzyl protective group by the addition …

[Tetrahedron, , vol. 54, # 46 p. 13981 - 13996]

Studies on peptides. CLII. Hard acid deprotecting procedure for peptide synthesis.

[Chemical and pharmaceutical bulletin, , vol. 35, # 8 p. 3447 - 3452]

More Articles...