Reactions of phenylthiotrimethylsilylmethyllithium: Preparation of α-phenylthioketones and additions to 2-cyclohexen-1-one
✍ Scribed by David J Ager
- Book ID
- 104241752
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 201 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Phenylthiotrimethylsilylmethyllithium(l) was reacted with a variety of electrophiles, including some containing two functional groups. o(-Phenylthioketones were obtained from the reaction with esters. The anion(l) underwent either 1,2-or l,&addition,depending on the conditions used, with 2-cyclohexen-l-one.
📜 SIMILAR VOLUMES
Preparation and Reactions of 2-Zincated 2-Cyclohexen-1-one and Related Heterocycles. -Conversion of 2-iodocyclohexenone (I) or the related heterocycles (IV) and (VII) to the corresponding iodo zinc derivatives followed by a catalyzed reaction with electrophiles generates a variety of new functional
## Abstract Relative rate coefficients for the reactions of OH with 3‐methyl‐2‐cyclohexen‐1‐one and 3,5,5‐trimethyl‐2‐cyclohexen‐1‐one have been determined at 298 K and atmospheric pressure by the relative rate technique. OH radicals were generated by the photolysis of methyl nitrite in synthetic a