Reaction of Cyclic Thioxocarbonates with Tributyltin Hydride(Organic,Chemical)
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概要
- 論文の詳細を見る
Treatment of methyl 2-О-acetyl-3,4-О-thiocarbonyl-β-L-arabinopyranoside with tributyltin hydride produced seven compounds, depending on the reaction conditions: the deoxy derivatives (2 and 3), the methylidene derivative (4), the carbonate (5), the О,S-rearrangement products (7 and 8), and the 4-deoxy acetyl migration product (9). Their structures were determined by spectroscopic and chemical means, and their formation mechanisms are discussed.
- 公益社団法人日本薬学会の論文
- 1987-09-25
著者
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Haque Mohammed
Research Institute For Wakan-yaku (oriental Medicines) Toyama Medical And Pharmaceutical University
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Tsuda Yoshisuke
Faculty Of Pharmaceutical Sciences Kanazawa University
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Kanemitsu Kimihiro
Faculty Of Pharmaceutical Sciences Kanazawa University
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TSUBONO Koji
Research Institute for Wakan-Yaku (Oriental Medicines), Toyama Medical and Pharmaceutical University
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Tsubono Koji
Research Institute For Wakan-yaku (oriental Medicines) Toyama Medical And Pharmaceutical University
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Kikuchi Tohru
Research Institute For Wakan-yaku (oriental Medicines) Toyama Medical And Pharmaceutical University
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KIKUCHI Tohru
Research Institute for Wakan-Yaku (Oriental Medicine), Toyama Medical and Pharmaceutical University
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