Conversion of 4-Oxoproline Esters to 4-Substituted Pyrrole-2-carboxylic Acid Esters
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概要
- 論文の詳細を見る
The Grignard, Wittig, Tebbe, Horner-Emmons, and Reformatsky reactions of the 4-oxoproline esters gave the corresponding 4-alylated or 4-alkylidenated products, respectively. The products were properly treated with bases to cause aromatization, giving 4-substituted pyrrole-2-carboxylic acid esters such as methyl 4-methylpyrrole-2-carboxylate, which is a trail pheromone of Atta texana.
- 公益社団法人日本薬学会の論文
- 2009-02-01
著者
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ARAKAWA Yasushi
Faculty of Pharmaceutical Sciences, Hokuriku University
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Yagi Naomi
Faculty Of Pharmaceutical Scicences Health Sciences University Of Hokkaido
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Yagi Naomi
Faculty Of Pharmaceutical Sciences Hokuriku University
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ARAKAWA Yukimi
Faculty of Pharmaceutical Sciences, Hokuriku University
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Yoshifuji S
Faculty Of Pharmaceutical Sciences Hokuriku University
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Yoshifuji Shigeyuki
Faculty Of Pharmaceutical Sciences Hokuriku University
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TANAKA Ken-ichi
Faculty of Pharmaceutical Sciences, Hokuriku University
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Arakawa Yasushi
Faculty Of Pharmaceutical Sciences Hokuriku University
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Tanaka Ken-ichi
Faculty Of Pharmaceutical Sciences Hokuriku University
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Tanaka Ken-ichi
Faculty of Engineering, Hokkaido University
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