Simple And Efficient Method For Synthesis Of Z-Boc-Amino Acid Amides Using P-Toluenesulphonyl Chloride

Title: Simple And Efficient Method For Synthesis Of Z-Boc-Amino Acid Amides Using P-Toluenesulphonyl Chloride

Volume: 8 Issue: 1

Author(s): Kuppanna Ananda, Ganga-Ramu Vasanthakumar and Vommina V. Suresh Babu

Affiliation:

Keywords: Boc-AMINO ACID, TOLUENESULPHONYL, luteinizing harmone, selective tosylation, layer chromatography, stirred solution, anhydrous sodium sulphate

Abstract: Amides of Z- and Boc protected amino acids have been prepared by using p-toluenesulphonyl chloride (TsCI) for the activation of carboxyl group. The resulting mixed carboxylic-sulphonic anhydride intermediate was treated in situ with an excess of 25 percent ammonia solution. All the amino acid amides prepared were obtained as crystalline solids in good yield and purity.

Cite this article as:

Ananda Kuppanna, Vasanthakumar Ganga-Ramu and Suresh Babu V. Vommina, Simple And Efficient Method For Synthesis Of Z-Boc-Amino Acid Amides Using P-Toluenesulphonyl Chloride, Protein & Peptide Letters 2001; 8 (1) . https://dx.doi.org/10.2174/0929866013409742