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Volumn 63, Issue 9, 1998, Pages 3037-3040

Optical resolution of 3-(silyloxy)glutaric acid half esters and their utilization for enantioconvergent synthesis of a HMG-CoA reductase inhibitor

Author keywords

[No Author keywords available]

Indexed keywords

GLUTARIC ACID DERIVATIVE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR;

EID: 0032080388     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9722156     Document Type: Article
Times cited : (7)

References (23)
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  • 4
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    • The Chemistry and Total Synthesis of Mevinic Acids
    • Lukacs, G., Ueno, S., Eds.; Springer: New York
    • For a review on synthetic work, see: Chapleur, Y. The Chemistry and Total Synthesis of Mevinic Acids. In Recent Progress in the Chemistry of Antibiotics; Lukacs, G., Ueno, S., Eds.; Springer: New York, 1993; Vol. 2; pp 829-937.
    • (1993) Recent Progress in the Chemistry of Antibiotics , vol.2 , pp. 829-937
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    • (c) Hirai, K.; Ishiba, T.; Koike, H.; Watanabe, M. Jpn. Kokai Tokkyo Koho JP 04-352767 [92-352767], 1992.
    • (1992)
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    • 14444276134 scopus 로고
    • Jpn. Kokai Tokkyo Koho JP 05-32680 [9332680]
    • Hirai, K.; Okada, T. Jpn. Kokai Tokkyo Koho JP 05-32680 [9332680], 1993; Chem. Abstr. 1993, 119, 138753e.
    • (1993)
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    • Hirai, K.; Okada, T. Jpn. Kokai Tokkyo Koho JP 05-32680 [9332680], 1993; Chem. Abstr. 1993, 119, 138753e.
    • (1993) Chem. Abstr. , vol.119
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    • 14444273957 scopus 로고    scopus 로고
    • Both enantiomers (99% ee) are now available through the cooperation of Shionogi & Co., Ltd. and Ube Industries, Ltd. For samples of (R)-1 and (S)-1, send inquiries to T. Hashimoto at Ube Industries, Ltd., 2-3-11, Higashi-Shinagawa, Shinagawa-ku, Tokyo 140, Japan
    • Both enantiomers (99% ee) are now available through the cooperation of Shionogi & Co., Ltd. and Ube Industries, Ltd. For samples of (R)-1 and (S)-1, send inquiries to T. Hashimoto at Ube Industries, Ltd., 2-3-11, Higashi-Shinagawa, Shinagawa-ku, Tokyo 140, Japan.
  • 16
    • 14444272838 scopus 로고
    • Jpn. Kokai Tokkyo Koho JP 07-118233 [95-118233]
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    • (1995)
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    • (1995) Chem. Abstr. , vol.123
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    • PCT Int. Appl., WO 92/22560
    • A part of this work has been published in the patent. Konoike, T.; Araki, Y. PCT Int. Appl., WO 92/22560, 1992; Chem. Abstr. 1993, 119, 95827n.
    • (1992)
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    • A part of this work has been published in the patent. Konoike, T.; Araki, Y. PCT Int. Appl., WO 92/22560, 1992; Chem. Abstr. 1993, 119, 95827n.
    • (1993) Chem. Abstr. , vol.119
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    • 8a using 3-methyl-2-butanone instead of ethyl 4-methyl-3-oxoheptanoate as a starting material
    • 8a using 3-methyl-2-butanone instead of ethyl 4-methyl-3-oxoheptanoate as a starting material.
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    • Enatiomeric excess was determined by HPLC; see ref 8
    • Enatiomeric excess was determined by HPLC; see ref 8.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.