Seandium(III) triflate-catalyzed allylation of earbonyi compounds with tetraallylgermane proceeded readily in aqueous nitromethane to afford homoaUyl alcohols in excellent to good yields. The presence of H2 O is indispensable for the allylation of aldehydes to proceed smoothly. Aldehydes were allyla
Aqueous reactions with a Lewis acid and an organometallic reagent. The scandium trifluoromethanesulfonate-catalyzed allylation reaction of carbonyl compounds with tetraallyltin
โ Scribed by Hachiya, Iwao; Kobayashi, Shu
- Book ID
- 126162432
- Publisher
- American Chemical Society
- Year
- 1993
- Tongue
- English
- Weight
- 243 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0022-3263
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๐ SIMILAR VOLUMES
Scandium(III) triflate-catalyzed allylation of carbonyl compounds with tetraallylgermane proceeded readily in aqueous nitromethane to afford homoallyl alcohols in excellent to good yields. The presence of H20 is indispensable for the allylation of aldehydes to proceed smoothly. Aldehydes were allyla
reactions of organo-metal compounds reactions of organo-metal compounds O 0350 38 -084 Scandium Trifluoromethanesulfonate Catalyzed Chemoselective Allylation Reactions of Carbonyl Compounds with Tetraallylgermane in Aqueous Media. -The Sc(O-Tf) 3 -catalyzed chemoselective allylation of carbonyl com