A Pratical Synthesis of Optically Active Atenolol from Chiral Epichlorohydrin
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概要
- 論文の詳細を見る
The synthesis of (R)- and (S)-atenolol (1) was achieved in two steps starting from p-hydroxyphenylacetamide (2). Both enantiomers of the glycidyl ether 4 were synthesized from 2 and (R)- and (S)-epichlorohydrin (3) using an alkali metal hydroxide and/or BTA (benzyltrimethylammonium chloride), respectively. Subsequent treatment of 4 with isopropylamine afforded atenolol (1) with excellent enantiomeric excess (>98% ee).
- 公益社団法人日本薬学会の論文
- 1997-02-15
著者
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Otera J
Department Of Applied Chemistry Okayama University Of Science
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Otera Junzo
Department Of Applied Chemistry Faculty Of Engineering Okayama University Of Science
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Yoshimoto H
Research Laboratories Of Daiso Co. Ltd.
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KITAORI Kazuhiro
Research Laboratories of Daiso Co., Ltd.,
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TAKEHIRA Yoshikazu
Research Laboratories of Daiso Co., Ltd.,
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FURUKAWA Yoshiro
Research Laboratories of Daiso Co., Ltd.,
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YOSHIMOTO Hiroshi
Research Laboratories of Daiso Co., Ltd.,
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Kitaori Kazuhiro
Research Laboratories Of Daiso Co. Ltd.
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Furukawa Y
Nagoya City Univ. Nagoya Jpn
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Takehira Yoshikazu
Research Laboratories Of Daiso Co. Ltd.
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