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  • Paraformaldehyde in a methanolic solution of KOH converts ketones into alpha-methoxymethylated and alpha- hydroxymethylated products. The method was tested on nine steroidal ketones. On prolonged treatment the ketones formed are reduced to alcohols.
  • Paraformaldehyde in a methanolic solution of KOH converts ketones into alpha-methoxymethylated and alpha- hydroxymethylated products. The method was tested on nine steroidal ketones. On prolonged treatment the ketones formed are reduced to alcohols. (en)
Title
  • alpha-Methoxymethyl ketones via aldol reaction
  • alpha-Methoxymethyl ketones via aldol reaction (en)
skos:prefLabel
  • alpha-Methoxymethyl ketones via aldol reaction
  • alpha-Methoxymethyl ketones via aldol reaction (en)
skos:notation
  • RIV/61388963:_____/13:00421183!RIV14-TA0-61388963
http://linked.open...avai/riv/aktivita
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  • I, P(TE01020028)
http://linked.open...iv/cisloPeriodika
  • 46
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
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  • 60149
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  • RIV/61388963:_____/13:00421183
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  • NMR; steroids; synthesis; aldol reaction (en)
http://linked.open.../riv/klicoveSlovo
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  • GB - Spojené království Velké Británie a Severního Irska
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  • [885D92077726]
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  • Tetrahedron
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http://linked.open...v/svazekPeriodika
  • 69
http://linked.open...iv/tvurceVysledku
  • Buděšínský, Miloš
  • Kasal, Alexander
http://linked.open...ain/vavai/riv/wos
  • 000326768800019
issn
  • 0040-4020
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.tet.2013.09.022
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