1-(alkylthio)-polyfluoroalkynes. Reactions with mercaptans and thermal transformations
✍ Scribed by Yuri G. Shermolovich; Vadim M. Timoschenko; Rostislav Ya. Musyanovich; Mark I. Povolotsky; Vladimir V. Pirozhenko; Leonid N. Markovsky
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 152 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
✦ Synopsis
1-(Alkylthio)difluoropropynes regioselectively add dialkylamines and mercaptans with formation of 1-(alkylthio)-2-dialkylamino(alkylthio)ethenes, which exist only in the form of one (presumably the trans isomer) geometrical isomer. Thermal transformation of 1-(alkylthio
)difluoropropynes occurs at a temperature of under 100ЊC and leads to the formation of 2,4bis(polyfluoroalkyl)-3-(alkylthio)thiophenes.
📜 SIMILAR VOLUMES
## Abstract 3‐Hydroxyquinoline‐2,4‐diones **1** react with isocyanates to give novel 1,2,3,4‐tetrahydro‐2,4‐dioxoquinolin‐3‐yl (alkyl/aryl)carbamates **2** and/or 1,9b‐dihydro‐9b‐hydroxyoxazolo[5,4‐__c__]quinoline‐2,4(3a__H__,5__H__)‐diones **3**. Both of these compounds are converted, by boiling i
## Abstract Reaction of diones (I) and (V) with isocyanates gives the hitherto unknown dioxoquinolinyl carbamates (III) and/or oxazolo[5,4‐c]quinolinediones (IV).