Lewis acid-promoted addition of methylenecyclopropanes to aldehydes and ketones
β Scribed by Katsukiyo Miura; Mizuki Takasumi; Takeshi Hondo; Hiroshi Saito; Akira Hosomi
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 242 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
In the presence of TiCi4, me~ylenecyclopropane (la) easily reacted with Jdln~u~tlc aldehydes to give the p-(chiorome~yl)allylate~ products 2 in good yields along with a small amount of the methylenetetrahydrofurans 3. The reacti~ with chiral a-and ~-alkoxy aldehydes lwoceeded with high levels of cl~latioG control.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
Rearrangement of trisubstituted epoxides has been effected under the influence of various Lewis acids. Among these, methylaluminum bis(4-bromo-2,6-di-t-butylphenoxide) (MABR) can be selectively rearranged from trisubstituted epoxides to aldehydes, while antimony pentafluoride is employable for selec