Thiosteroids. XXI. Episulfide Formation from Vicinal Thiocyanatohydrins and Their Acetates

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概要

• 論文の詳細を見る

• Each epimers of 2,3-episulfides of 5β, 25D-spirostane and 17β-hydroxy-5α-androstanes having a methyl group at C-1α, C_2,or C_3 were synthesized via the corresponding vicinal diaxial thiocyanatohydrins. In addition the formation of both episulfides and oxides from the vicinal diaxial thiocyanatohydrin acetates was discussed on the basis of the natures of the substituents.

• 社団法人日本薬学会の論文
• 1969-10-25

著者

• 武田 健一

  Shionogi Research Laboratory Shionogi & Co. Ltd.

• 米野 太一郎

  Shionogi Research Laboratory, Shionogi & Co., Ltd.

• 石原 照一

  Shionogi Research Laboratory, Shionogi & Co., Ltd.

• 井谷 光

  Shionogi Research Laboratory, Shionogi & Co., Ltd.

• 岩倉 彦三

  Shionogi Research Laboratory, Shionogi & Co., Ltd.

• 武田 健一

  塩野義製薬(株)

• 武田 健一

  Research Laboratory Shionogi & Co. Ltd.

• 武田 健一

  塩野義研

• Takeda Ken'ichi

  Shionogi Research Laboratory Shionogi & Co. Ltd.

• 岩倉 彦三

  Shionogi Research Laboratory Shionogi & Co. Ltd.

• 井谷 光

  Shionogi Research Laboratories Shionogi & Co. Ltd.

• 石原 照一

  Shionogi Research Laboratory Shionogi & Co. Ltd.

• 米野 太一郎

  Shionogi Research Laboratory Shionogi & Co. Ltd.

• 武田 健一

  Shionogi Research Laboratories

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