The addition of a catalytic amount of Cp2TiC12 to an ether solution of propylmagnesium bromide and 1,3-dienes brings about an
Cp2TiCl2-Catalyzed Grignard exchange reactions with acetylenes. A convenient method for preparation of E-alkenyl Grignard reagents
β Scribed by Fumie Sato; Hiroaki Ishikawa; Masao Sato
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 229 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
A variety of triflates containing a 8-oxygen functionality were efficiently reacted with Grignard reagents in the presence of CuBr to afford the corresponding coupling products. We have recently described a strategy for preparing cis-or trans-di-
Treatment of Cl2ZrCp2 with 2 equiv of alkylmetals (RM) containing Li or Mg, e.g., n-BuLi, in THF produces organozirconium species that act as sources of "ZrCp2," the latter product being a convenient reagent for preparing zirconacycles. We recently reported a bicyclization reaction of enynes3 with