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Lewis acid-promoted addition of methylenecyclopropanes to aldehydes and ketones

✍ 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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✦ 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.


πŸ“œ SIMILAR VOLUMES


Lewis acid-promoted selective rearrangem
✍ Keiji Maruoka; Noriaki Murase; Ronan Bureau; Takashi Ooi; Hisashi Yamamoto πŸ“‚ Article πŸ“… 1994 πŸ› Elsevier Science 🌐 French βš– 613 KB

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