Short-route Synthesis of a Glycerophospholipid Bearing an Unsaturated Acyl Group at the sn-1 Position
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概要
- 論文の詳細を見る
A short-route synthesis of an optically active phosphocholine bearing an unsaturated acyl group at the sn-1 position was developed via lipase-catalyzed enantioselective acylation of 2-O-methoxyeth-oxymethylglycerol, removal of the MEM group by employing cat-echol boron bromide, subsequent DCC-mediated acylation of the hydroxy group at the 2-position and final introduction of a choline phosphate moiety.
- 社団法人日本農芸化学会の論文
- 1995-02-23
著者
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Nakajima S
Graduate School Of Natural Science And Technology Okayama University
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Nakajima Shuhei
Department Of Bioresources Chemistry Faculty Of Agriculture Okayama University
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Baba Naomichi
Department Of Bioresources Chemistry Faculty Of Agriculture Okayama University
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Baba Naomichi
Department Of Biore Sources Chemistry Faculty Of Agriculture Okayama University
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Tahara S
Department Of Applied Bioscience Faculty Of Agriculture Hokkaido University
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Tahara Satoshi
Hokkaido Univ. Sapporo Jpn
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Tahara S
Hokkaido Univ. Sapporo Jpn
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Tahara Satoshi
Division Of Applied Bioscience Graduate School Of Agriculture Hokkaido University:crest Japan Scienc
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Akiyama Takeshi
Department of Bioresources Chemistry, Faculty of Agriculture, Okayama University
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Tahara Shoichi
Department of Bioresources Chemistry, Faculty of Agriculture, Okayama University
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Nakajima Shuhei
Department Of Agricultural Science Okayama University
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Baba Naomichi
Div. Of Bioscience Graduate School Of Natural Sci. And Technol. Okayama Univ.
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Tahara S
Tokyo Metropolitan Inst. Of Gerontology
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Akiyama T
Nara Inst. Of Sci. And Technol. Nara Jpn
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Akiyama Takeshi
Department Of Biology Faculty Of Science Toyama University
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BABA Naomichi
Department of Biofunctional Chemistry, Graduate School of Natural Science and Technology, Okayama University
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