The novel reaction of 1-chloro-2-(α-bromoethyl)hexafluorocyclopentene-1 with Grignard reagents
✍ Scribed by Joseph D. Park; Randolph J. McMurtry
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- French
- Weight
- 248 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
l-C"nZoro-Z-methyZ-N,N-tetrarnethylenepropenyZcnnine was found to be a good condensatioz reagent for a regioselective coupling reaction of a2132 aZeohoZs with Grignard reagents under mitd conditions to afford olefinic products. The allylic unit is a common structural feature of many natural compoun
The Grignard reagent from racemic l-chloro-2-phenylbutane has been partially resolved by allowing it to react with less than one equivalent of one of several readily available chiral ketones. Reaction with approximately 0.5 equivalents(2) of (+)-camphor, (-)-fenchone, (-)-menthone or (+)-3-methylcyc
It has been reported that the reaction of halogenoazulenes with some nucleophilic reagents gave the corresponding substitution products by replacement of the halogen0 substituents with the reagents (1, 2, 3). However, no report has