Nucleophilic reactions of propargyl acetates mediated by titanocene dichloride and magnesium
โ Scribed by Fanglong Yang; Gang Zhao; Yu Ding
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 86 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Reaction of Cp 2 TiCl 2 /Mg with propargyl acetates form allenyl titanium intermediates, which undergo nucleophilic addition reactions to aldehydes or ketones to give homopropargyl alcohols in high yields. Subsequent nucleophilic addition to acetonitrile and nucleophilic substitution with allyl bromide are also mentioned.
๐ SIMILAR VOLUMES
Indium mediated allylation and propargylation reactions of acetals and ketals with various allyl or propargyl bromides in aqueous media successfully provided the corresponding homoallylic or homopropargylic (and allenylic) alcohol, respectively, in moderate to good yields. Highly chemoselective ally