p-Toluenesulfonyl Chloride Catalysed Facile Synthesis of O-benzyl-l-amino Acids and Their In Vitro Evaluation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Molecular Medicine,Biochemistry,Bioengineering,Analytical Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s10989-019-09998-x.pdf
Reference14 articles.
1. Arai I, Muramatsu I (1982) A simple and convenient method for esterification of Tryptophan and other amino acids. J. Org. Chem. 48:121–123
2. Bolchi C, Valoti E, Fumagalli L, Straniero V, Ruggeri P, Pallavicini M (2015) Enantiomerically pure dibenzyl esters of L-aspartic and L-glutamic acid. Org Process Res Dev 19:878–883
3. Bolchi C, Bavo F, Pallavicini M (2017) One-step preparation of enantiopure L- or D-amino acid benzyl esters avoiding the use of banned solvents. Amino Acids 49:965–974
4. Bolchi C, Bavo F, Regazzoni L, Pallavicini M (2018) Preparation of enantiopure methionine, arginine, tryptophan, and proline benzyl esters in green ethers by Fischer-Speier reaction. Amino Acids 50:1261–1268
5. Chemicalbook (2019a) p-Toluenesulfonic acid. https://www.chemicalbook.com/ProductChemicalPropertiesCB1771154_EN.htm. Accessed 20 June 2019
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