This communication reports, inter alia, the following remarkable transformation: -- ## IN RCN (Solvent) < 1. Analysis in excellent accord substance 2. A. Hassner, Act. Chem. Res.,
Solvent participation in additions to olefins
β Scribed by Fred Boerwinkle; Alfred Hassner
- Book ID
- 104213835
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 194 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
In the course of our study of the addition reactions of discovered that the solvent can enter into the reaction very adduct derived from bromine and solvent. 3 We have been able conditions so that the incorporation of solvent can occur to
π SIMILAR VOLUMES
## Under carefully chosen working conditions (solvent, temperature), methyltitanium reagents smoothly convert homoallyl alcohols having a terminal double-bond into (El-3-penten-1-01s whereas non-terminal a-alken-1-01s afford I-methyl-branched derivatives with configurational inversion of the chain (
## The medicinal poteatfal of Eluorosteroids 192 prompted CF, additions to steroidal olefins, 2-4 but there has been no examination of their relative reactivities toward CFa, nor have these reactivities been related to those of the common alkenes. 5 Such information is important in synthetic plann