Stereoselective Synthesis of 2, 4-Diamino Acids by Asymmetric Hydrogenation

NG Park, S Lee, H Maeda, H Aoyagi…

Index: Park, Nam Gyu; Lee, Sannamu; Maeda, Hiroshi; Aoyagi, Haruhiko; Kato, Tetsuo Bulletin of the Chemical Society of Japan, 1989 , vol. 62, # 7 p. 2315 - 2319

Full Text: HTML

Citation Number: 13

Abstract

A stereoselective synthesis of unusual basic amino acids, ornithine, 2, 4-diaminopentanoic acid, and 2, 4-diamino-6-methylheptanoic acid, was achieved by the hydrogenation of cyclic α, β-dehydro dipeptides obtained by the condensation of cyclo (–Gly–L (or D)-aminoacyl–) and protected linear or chiral amino aldehydes. The degree of chiral induction greatly depended on the bulkiness of the side chains of α, β-dehydro amino acids. The R f values ...

Related Articles:

Identification of new peptide amides as selective cathepsin L inhibitors: The first step towards selective irreversible inhibitors?

[Bioorganic and Medicinal Chemistry Letters, , vol. 23, # 10 p. 2968 - 2973]

Stereoselective Synthesis of 2, 4-Diamino Acids by Asymmetric Hydrogenation

[Bulletin of the Chemical Society of Japan, , vol. 62, # 7 p. 2315 - 2319]

Kinetic behavior of L-arginine in the interlamellar layer of montmorillonite in aqueous suspension

[Journal of Physical Chemistry, , vol. 88, # 6 p. 1253 - 1257]

Structure and biosynthetic assembly of cupriachelin, a photoreactive siderophore from the bioplastic producer Cupriavidus necator H16

[Journal of the American Chemical Society, , vol. 134, # 11 p. 5415 - 5422]

Sun light initiated changes in aqueous solution of lysine under heterogeneous conditions

[Journal of the Indian Chemical Society, , vol. 66, # 11 p. 828 - 829]

More Articles...