Stereoselective Construction of Tetra-Substituted Tetrahydrofuran Compounds from Benzylic Hemiacetal in the Presence of H_2 and a Pd Catalyst : Stereoselective Synthesis of a Stereoisomer of (-)-Virgatusin and Its Antimicrobiological Activity
スポンサーリンク
概要
- 論文の詳細を見る
Tetra-substituted tetrahydrofuran compounds were stereoselectively prepared from benzylic hemiacetal in the neutral condition by employing the simple reagent, H2, and a Pd catalyst. The stereoselective conversion of benzylic hemiacetal to two different stereoisomers of the tetrasubstituted tetrahydrofuran compound was observed. One of these tetrahydrofuran compounds was converted to the virgatusin stereoisomer to estimate its antimicrobiological activity.
- 社団法人 日本農芸化学会の論文
- 2008-01-23
著者
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SUGAHARA Takuya
Faculty of Agriculture, Ehime University
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Akiyama Koichi
Faculty Of Agriculture Ehime University
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Akiyama Koichi
Integrated Center For Sciences Tarumi Station Ehime Univ.
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Sugahara Takuya
Faculty Of Agriculture Ehime University
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YAMAUCHI Satoshi
Faculty of Agriculture, Ehime University
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MARUYAMA Masafumi
Faculty of Agriculture, Ehime University
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KISHIDA Taro
Faculty of Agriculture, Ehime University
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Nakato Tomofumi
Faculty of Agriculture, Ehime University
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Tago Ryosuke
Faculty of Agriculture, Ehime University
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Kishida Taro
South Ehime Fisheries Res. Center
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Sugahara Takuya
Fac. Of Agriculture Ehime Univ.
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Kishida Taro
Faculty Of Agriculture Ehime University
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Yamauchi Satoshi
Faculty Of Agriculture Ehime University
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Akiyama Koichi
Integrated Center For Sciences (incs) Ehime University
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Maruyama Masafumi
Faculty Of Agriculture Ehime University
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Nakato Tomofumi
Faculty Of Agriculture Ehime University
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Tago Ryosuke
Faculty Of Agriculture Ehime University
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Yamauchi Satoshi
Fac. Of Agriculture Ehime Univ.
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Maruyama Masafumi
Fac. Of Agriculture Ehime Univ.
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