## Abstract For Abstract see ChemInform Abstract in Full Text.
Solvent-controlled additions of organotitanium reagents to olefinic double bonds
✍ Scribed by Etienne Moret; Manfred Schlosser
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 216 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
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 (2 + E; E + Z), stereoselectivities being better than 99%.
Recently we have disclosed a procedure for the titanium-mediated methylation of homoallyl alco-This work was supported by the Schweizerische Nationalfonds zur Forderung der wissenschaftlichen Forschung, Bern (grant nr. 2.635-0.82).
📜 SIMILAR VOLUMES
Reactive (ally1 and benzyl) Grignard reagents have been shorn to add to the double bond of allylic alcohols (I; Rv = H or Ar); the intermediates foraed in this reaction are probably the cyclic adducts II, vhich are themselves Grignard reagents and lead to a variety of products when treated vith suit
## Abstract A new method for the synthesis of tin‐carbon bonds is described. The synthesis involves the non‐catalysed addition of organo‐tin hydrides to olefinic double bonds at moderate temperatures (60–100°). This method allows the preparation of a variety of hitherto unknown types of functionall