Trimethylsilylethynyl ketones as surrogates for ethynyl ketones in the double Michael reaction.
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| Abstract | :  Trimethylsilylethynyl ketones can be desilylated in the presence of a tethered carbon diacid and induced to undergo a double Michael reaction in situ. The trimethylsilylethynyl ketones can serve as surrogates of ethynyl ketones that are difficult to prepare or isolate. | 
| Year of Publication | :  2002 | 
| Journal | :  The Journal of organic chemistry | 
| Volume | :  67 | 
| Issue | :  9 | 
| Number of Pages | :  3149-51 | 
| Date Published | :  2002 | 
| ISSN Number | :  0022-3263 | 
| URL | :  https://dx.doi.org/10.1021/jo0163086 | 
| DOI | :  10.1021/jo0163086 | 
| Short Title | :  J Org Chem | 
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