Uncatalyzed insertion reaction of isocyanides into a carbon-sulfur bond
β Scribed by G. Morel; E. Marchand; K.H. Nguyem Thi; A. Foucaud
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 194 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
swmvlry Tert-butylzsocyanide and tert-0ctyZieocyanzde insert znto the carbone-eutftcr bond of actzvated sulfuies 2 yiekizng thzoimidatee S which rearmnge to enamnes g.
π SIMILAR VOLUMES
A solution of ( I l i ) (10 g, 19.3 mmol) in 80 ml of anhydrous toluene, which contains 5 ml ethanol, is heated under reflux for 12 h. The solvent is removed and the residue digested with 50 ml pentane. Precipitated Ph3P0 is separated off and the previously unknown 4,5,6,6a-tetrahydro-2( 1 H)-pental
We have reported a series of insertion reactions of isocyanides into nitrogen-hydrogen of amine.1) oxygen-hydrogen of alcohol, 2) sulfur-hydrogen of thiol, 3) and silicone-hydrogen of silane4) to produce the corresponding derivatives of N-alkylformimidic acid in high yields.