Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5222518 | Tetrahedron | 2011 | 7 Pages |
Abstract
An easy, efficient, and simple one-pot approach for the synthesis of 1,3-thiazolidine-2-thiones via multicomponent reaction is reported. The reaction of a primary amine with carbon disulfide in the presence of dibenzoylacetylene or bis(4-methyl-1-benzoyl)acetylene in a mixture of CH2Cl2 and H2O after 5Â h, afforded the title compound as alkene diastereomers.
Graphical abstractA facile and direct synthetic entry to 1,3-thiazolidine-2-thione derivatives is reported which involves the three-component coupling of carbon disulfide, primary amines and dibenzoylacetylene or bis(4-methyl-1-benzoyl)acetylene under neutral conditions in a mixture of CH2Cl2 and H2O.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Abdolali Alizadeh, Nasrin Zohreh, Hamideh Sabahnoo, Zohreh Noaparast,