Literature DB >> 24978059

Decarboxylative thioamidation of arylacetic and cinnamic acids: a new approach to thioamides.

Tirumaleswararao Guntreddi1, Rajeshwer Vanjari, Krishna Nand Singh.   

Abstract

A new decarboxylative strategy has been developed for the synthesis of thioamides via a three-component reaction involving arylacetic or cinnamic acids, amines and elemental sulfur powder, without the need of a transition metal and an external oxidant.

Entities:  

Year:  2014        PMID： 24978059     DOI： 10.1021/ol501482g

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  3 in total

1.  Cellulose-reinforced poly(ethylene-co-vinyl acetate)-supported Ag nanoparticles with excellent catalytic properties: synthesis of thioamides using the Willgerodt-Kindler reaction.

Authors:  Anoop Singh; Sanjeev Saini; Narinder Singh; Navneet Kaur; Doo Ok Jang
Journal:  RSC Adv       Date:  2022-02-25       Impact factor: 3.361

2.  Homo-condensation of acetophenones toward imidazothiones.

Authors:  Phuc Hoang Pham; Phuc Thai Thien Nguyen; Thuy Thu Bui; Hien Nhat Tra; Tung Thanh Nguyen; Nam Thanh Son Phan
Journal:  RSC Adv       Date:  2020-11-04       Impact factor: 4.036

3.  Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides.

Authors:  Weibing Liu; Cui Chen; Hailing Liu
Journal:  Beilstein J Org Chem       Date:  2015-09-23       Impact factor: 2.883
  3 in total

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