Literature DB >> 20349994

Super silyl stereo-directing groups for complete 1,5-syn and -anti stereoselectivities in the aldol reactions of beta-siloxy methyl ketones with aldehydes.

Yousuke Yamaoka1, Hisashi Yamamoto.   

Abstract

In this communication, we report that substrate-controlled 1,5-syn and -anti stereoinduction in the aldol reaction of beta-tris(trialkylsilyl)siloxy methyl ketones can be achieved with high diastereoselectivities. Tris(trialkylsilyl)silyl groups are easily prepared and play an important role in the selectivities of these reactions. Furthermore, all of the 1,3,5-triol stereoisomers can easily be prepared from beta-siloxy methyl ketones in no more than three steps.

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Year:  2010        PMID: 20349994      PMCID: PMC2868325          DOI: 10.1021/ja101076q

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  34 in total

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9.  Lewis base catalyzed aldol additions of chiral trichlorosilyl enolates and silyl enol ethers.

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  10 in total

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  10 in total

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