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Synlett 2013; 24(6): 775-776
DOI: 10.1055/s-0032-1317796
DOI: 10.1055/s-0032-1317796
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Mercaptoacetic Acid
Further Information
Publication History
Publication Date:
08 March 2013 (online)
Introduction
Mercaptoacetic acid (3), also known as thioglycolic acid, is a liquid miscible with water and with most organic solvents such as alcohols, ether, chloroform and benzene.[ 1 ] It is widely described in the literature, especially as a substrate for the synthesis of pharmacologically active heterocycles[ 2 ] including 1,3-thiazolidin-4-ones,[ 3 ] 1,4-thiazepines[ 4 ] and thiazoles.[ 5 ] It is also used for the formation of spiro derivatives,[ 6 ] in multicomponent reactions, and in removing the nosyl protecting group from amine functions of α-amino acids.[ 7 ]
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References
- 1 O’Neil MJ, Heckelman PE, Koch CB, Roman KJ, Kenny CM, D’Arecca MR. The Merck Index 14th Ed. . Merck Research Laboratories; New York: 2006
- 2 Yadav LD. S, Rai A. Tetrahedron Lett. 2008; 49: 5751
- 3 Gomes CR. B, Moreth M, Facchinetti V, De Souza MV. N, Vellasco JúniorW. T, Lourenço MC. S, Cunico W. Lett. Drug Des. Discovery 2010; 7: 353
- 4 Shi F, Zeng X.-N, Cao X.-D, Zhang S, Jiang B, Zheng W.-F, Tu S.-J. Bioorg. Med. Chem. Lett. 2012; 22: 743
- 5 Ayyad S.-EN, El-Taweel FM. A, Elagamey A.-GA, El-Mashad TM. Int. J. Org. Chem. 2012; 2: 135
- 6 Panda SS, Jain SC. Monats Chem. 2012; 143: 1187
- 7 Leggio A, Di Gioia ML, Perri F, Liguori A. Tetrahedron 2007; 63: 8164
- 8 Islamgulova VR, Shitova EN, Akhmerova SG, Tomilov AP. Russ. J. Appl. Chem. 2002; 9: 1470