A One-Pot Synthesis of Ketones and Aldehydes from Carbon Dioxide and Organolithium Compounds
β Scribed by Dipl.-Chem. Guido Zadel; Prof. Eberhard Breitmaier
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 253 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
β¦ Synopsis
obtained with the expensive Wilkinson catalyst ([
π SIMILAR VOLUMES
a-Formylc~clo/iexurtrune: A solution of 73 g of dimethylforniamide in 300 g of dichloromethane is stirred with exclusion of moisture at 5-10Β°C, and a solution of 100 g of phosgene in 300 g of dichloromethane is added dropwise. The mixture is left standing for 3 h, and then 167 g of I-morpholinocyclo
The unsuccessful synthesis of conjugated β£-oxoketene dithioic acids.
A convienent one-pot synthesis of macrocycles containing a bis(thiocarbamoyl) derivatives 3. In the final step, a ringclosure reaction using a large number of Ξ±,Ο-dielectrophilic tetraaminoethene substructure is described. Starting from oxalic amidines 1, reduction with lithium and subsequent buildi
## Abstract The synthesis of C~2~βoxygenates such as ethanol and acetic acid accomplished by CH~4~ dissociation and subsequent CO~2~ insertion onto methyl radicals, named the stepwise reaction technology, has been demonstrated to be both feasible and efficient through initial experiments conducted