Thiocyanoacetate. I. Reactions of Thiocyanoacetic Esters with Aldehydes
スポンサーリンク
概要
- 論文の詳細を見る
Thiocyanoacetic esters (I) and aldehydes reacted in the presence of potassium fluoride or carbonate to give α,β-unsaturated ester as a major product and an unexpected solid product (II) as a minor one, which was determined to be <I>N</I>-carbamoyl-2-imino-5-substituted 1,3-oxathiolane-4-carboxylic esters.
- 公益社団法人 日本化学会の論文
著者
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Kambe Satoshi
Oyama Technical College
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Midorikawa Hiroshi
The Institute of Physical and Chemical Research
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Hayashi Toshio
The Institute of Physical and Chemical Research
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Yasuda Heinosuke
The Institute of Physical and Chemical Research
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- The Syntheses of Heterocyclic Compounds by the Ternary Condensation of Malononitrile, Salicylaldehyde, and Aliphatic Ketones in the Presence of Ammonium Acetate
- The Reaction of Ethyl Ethoxymethylenecyanoacetate with Its Hydrazino Derivatives
- The Formation of Pyrazolo[1,5-a]pyrimidine Derivatives
- The Cyclization Products from Acetone with Cyanoacetic Esters
- Mass Spectra of 2-Thioxo-Pyrimidine Derivatives
- Reactions of Acetoin and Benzoin with Malononitrile
- Thiocyanoacetate. I. Reactions of Thiocyanoacetic Esters with Aldehydes
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- Synthesis of 3-(alkoxycarbonylmethylthio)coumarins from thiocyanatoacetic esters and salicylaldehydes.