Pregledni rad

2-Thiazolin-5-thiones, a New Type of Sulfur Heterocycle Synthesis and Reactions

Heinz Heimgartner ; Institute of Organic Chemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland

Sažetak

Simple syntheses of 4,4-disubstituted 2-thiazolin-5-thiones, which have so far been difficult to obtain, are described. These compounds are stable and undergo a number of different reactions. The first type of reaction discussed here are cyclosubstitutions, which occur on heating in the presence of electron-deficient acetylenes. 1,3-Dithiafulvenes are thus formed via nitrile elimination. Thiazolinthiones show different chemical behaviour in reactions with ynamines. On warrning, thiazolinylidene-thioamides and -thioketones are formed via a [2+2] cycloaddition, followed by an electrocyclic ring opening reaction. The third reaction type has been observed in the conversion with 1,3-dipolar reagents, In situ generated benzonitriliumbetaines undergo 1,3-dipolar cycloaddition to the exocyclic e,S-double bond and form dithiaspiro
[4.4]nonadienes.

Ključne riječi

Hrčak ID:

177592

URI

https://hrcak.srce.hr/177592

Datum izdavanja:

16.5.1986.

Posjeta: 966 *