Synthesis of 3-silyl-2(5H)-furanone by rhodium-catalyzed cyclocarbonylation
β Scribed by Yukimasa Fukuta; Isamu Matsuda; Kenji Itoh
- Book ID
- 104211728
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 87 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
3-Silyl-2(5H)-furanones are readily formed by the rhodium-catalyzed cyclocarbonylation of propargyl alcohol derivatives bearing a trialkylsilyl group on the terminal sp-carbon under hydroformylation conditions. The following two requirements must be satisfied for the success of this protocol; (i) the presence of a silyl group on the sp-carbon, and (ii) the presence of a catalytic amount of Rh 4 (CO) 12 .
π SIMILAR VOLUMES
The reaction of (Z)-3-iodo-3-trifluoromethyl allylic alcohols 2 and CO in the presence of catalytic Pd(PPh 3 ) 4 afforded 3-trifluoromethyl-2(5H)-furanones (g-lactones) 3.