STEREOSELECTIVE 1,4-DIPOLAR CYCLOADDITIONS OF 2-(METHYLTHIO)-3,6-DIHYDRO-3,5-DIMETHYL-6-OXO-1-SUBSTITUTED PYRIMIDINIUM-4-OLATES WITH ALKENES
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概要
- 論文の詳細を見る
Reaction of 2-(methylthio)-3,6-dihydro-3,5-dimethyl-6-oxo-1-aryl- and alkyl-1-pyrimidinium-4-olates (1a-d) with alkenes carrying electron withdrawing groups gave 1,4-cycloadducts in good yields, demonstrating that 1,4-dipolar cycloaddition reaction proceeds with regio- and diastereoselectivity.
- 社団法人日本薬学会の論文
- 1995-04-15
著者
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太田 明廣
東京薬科大学薬学部
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太田 明廣
Tokyo College Of Pharmacy
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青柳 裕
東京薬科大学薬学部
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岡崎 文彰
Tokyo University of Pharmacy and Life Science, School of Pharmacy
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山野井 淑子
Tokyo University of Pharmacy and Life Science, School of Pharmacy
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前田 美紀子
Tokyo University of Pharmacy and Life Science, School of Pharmacy
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青柳 裕
Tokyo University of Pharmacy and Life Science, School of Pharmacy
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栗原 照夫
Faculty of Science, Josai University
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〓 桂林
Faculty of Science, Josai University
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栗原 照夫
Faculty Of Science Josai University
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太田 明廣
Department Of Pharmacognosy Tokyo College Of Pharmacy
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〓 桂林
Faculty Of Science Josai University
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Pang Gui-lin
Faculty Of Science Josai University
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前田 美紀子
Tokyo University Of Pharmacy And Life Science School Of Pharmacy
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Maeda Mikiko
Tokyo University Of Pharmacy And Life Science School Of Pharmacy
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岡崎 文彰
Tokyo University Of Pharmacy And Life Science School Of Pharmacy
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Okazaki Fumiaki
Tokyo University Of Pharmacy And Life Science School Of Pharmacy
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Aoyagi Y
Tokyo University Of Pharmacy And Life Science School Of Pharmacy
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山野井 淑子
Tokyo University Of Pharmacy And Life Science School Of Pharmacy
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