Facile routes to boron enolates. Et3B-mediated Reformatsky type reaction and three components coupling reaction of alkyl iodides, methyl vinyl ketone, and carbonyl compounds

書誌事項

公開日
1988
権利情報
  • https://www.elsevier.com/tdm/userlicense/1.0/
  • https://www.elsevier.com/legal/tdmrep-license
DOI
  • 10.1016/0040-4039(88)85330-9
  • 10.1002/chin.198830134
公開者
Elsevier BV

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説明

<jats:title>Abstract</jats:title><jats:p>The phenacyl halides (I) react with the oxo compounds (II) in the presence of triethylboron and triphenyltin hydride to give the ketols (III).</jats:p>

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