A Mild and Efficient Preparation of Carbodiimides
β Scribed by Fell, Jay B.; Coppola, Gary M.
- Book ID
- 120168754
- Publisher
- Taylor and Francis Group
- Year
- 1995
- Tongue
- English
- Weight
- 161 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0039-7911
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract Carbodiimides are formed with simultaneous evolution of CO~2~ by the reaction of basic catalyst with sterically hindered isocynates. Another generally applicable synthesis of carbodiimides involves intermediate formation of cyclic adducts of isocyanates and carbodiimides, which, upon cl
The preceding paper (1) ha8 described that the oxidation of mercaptans to diaulfidee by means of diethyl azodicarboxylate is extremely promoted by triphenyl phoaphine rithout being changed itself. A tautomeric pair of thiol and thiocarbonyl structures exists in a thiourea. Thus, the re-