On the esr identification of diphenylmethyl and 9-fluorenyl
β Scribed by F.A. Neugebauer; W.R. Groh
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 184 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
9-Fluorenyl carbocations substituted with the oxime functional groups CH=NOCH 3 , CH 3 C=NOCH 3 , and i-PrC=NOCH 3 were generated by solvolyses of the corresponding chlorides in methanol. These cations form at rates which greatly exceed those of formation of the parent 9-fluorenyl cation. Relative r
The title compounds, viz. C 13 H 8 (R)Ge (OCHMeCH 2 ) 3 N (1: R = H, 2: R = Me 3 Si; 3: R = Me 3 Ge) were prepared as mixtures of diastereomers by the reaction of N(CH 2 CHMeOSnAlk 3 ) 3 (7: Alk = Et; 8: Alk = Bu) with C 13 H 8 (R)GeBr 3 (4: R = H, 5: R = Me 3 Si; 6: R = Me 3 Ge), respectively. The