Rhenium-catalyzed reaction of carbonyl compounds with ketene silyl acetals
β Scribed by Yutaka Nishiyama; Kenta Kaiba; Rui Umeda
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 209 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
It was found that rhenium complex is an effective catalyst for the reaction of carbonyl compounds with ketene silyl acetals. A wide range of b-silyloxy esters is obtained by the treatment of carbonyl compounds with ketene silyl acetals in the presence of a catalytic amount of ReBr(CO) 5 in moderate to good yields.
π SIMILAR VOLUMES
## Abstract Theoretical calculations at the DFT level indicate that the reaction of a nitrone with a silyl ketene acetal proceeds, contrary to previous suggestions, through a classical 1,3βdipolar cycloaddition, followed by a silyl group transfer step to give the openβchain product. Introduction of