The Influence of Ligand Side Chain on the Enantioselectivity of Lewis Acid Catalyzed Diels-Alder Reactions
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概要
- 論文の詳細を見る
The enantioselective Lewis acid-catalyzed Diels-Alder reaction of 3-(2-propenoyl)-1,3-oxazolidin-2-one 8 with cyclopentadiene was examined using a series of chiral mox ligands 2-6, deferring in the side chain at 2-position of the chiral oxazoline and in the nature of the substituent at the chiral center (4-position) of the oxazoline ring, and a combination of N-[(1R)-2-chloro-1-phenylethyl]-2-[(4R)-4-phenyl-4,5-dihydrooxazol-2-yl]butyramide 2-Mgl_2-I_2 was the most efficient catalyst.
- 公益社団法人日本薬学会の論文
- 2002-09-01
著者
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Honda Y
Faculty Of Pharmaceutical Sciences Josai University
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Honda Yuko
Faculty Of Pharmaceutical Sciences Josai University
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Yamauchi Masashige
Faculty of Pharmaceutical Science,Josai University
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ITAI Kazuhiro
Faculty of Pharmaceutical Sciences, Josai University
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Itai Kazuhiro
Faculty Of Pharmaceutical Sciences Josai University
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Yamauchi Masashige
Faculty Of Pharmaceutical Science Josai University
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Yamauchi M
Faculty Of Pharmaceutical Sciences Josai University
関連論文
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- The Influence of Ligand Side Chain on the Enantioselectivity of Lewis Acid Catalyzed Diels-Alder Reactions
- Synthesis of 1-Hydroxybicyclo[3.2.1]oct-3-en-2-ones by Acyloin Rearrangement of 1-Methoxy- or 1-tert-Butyldimethylsilyloxy-bicyclo[2.2.2]oct-5-en-2-ones
- Reactivity of 2-Methylene-1, 3-dicarbonyl Compounds. 1, 3-Dipolar Cycloaddition Reaction with Ethyl Diazoacetate
- Base-promoted Acyloin Rearrangement of 1,8-Di-tert-butyldimethylsilyl-oxybicyclo[2.2.2]oct-5-en-2-ones
- Photochemical Synthesis of Bicyclo[4.1.0]hept-2-enes