Literature DB >> 26825297

A green synthesis in water of novel (1,5,3-dithiazepan-3-yl)alkanoic acids by the multicomponent reaction of amino acids, CH2O, and 1,2-ethanedithiol.

Guzel R Khabibullina1, Ekaterina S Fedotova2, Vnira R Akhmetova3, Ekaterina S Mesheryakova2, Leonard M Khalilov2, Askhat G Ibragimov2.   

Abstract

A library of new (1,5,3-dithiazepan-3-yl)alkanoic acids was prepared by the multicomponent cyclocondensation of amino acids, formaldehyde, and 1,2-ethanedithiol in water at room temperature for 1 to 5 h in high yields. This green procedure offers several advantages such as an operational simplicity, no catalyst, and no production of hazardous materials.

Entities:  

Keywords:  (1,5,3-Dithiazepan-3-yl)alkanoic acids; Amino acids; Green synthesis; MRCs; Multicomponent reaction; Water

Mesh:

Substances:

Year:  2016        PMID: 26825297     DOI: 10.1007/s11030-016-9656-0

Source DB:  PubMed          Journal:  Mol Divers        ISSN: 1381-1991            Impact factor:   2.943


  13 in total

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10.  Preparation and anticonvulsant activity of a series of functionalized alpha-heteroatom-substituted amino acids.

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