Synthetic Studies of 18-Membered Antitumor Macrolide, Tedanolide. 2. Stereoselective Synthesis of the C1-C7 Fragment via a Mismatched but Highly Efficient Sharpless Dihydroxylation
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概要
- 論文の詳細を見る
The C1-C7 fragment (4) of tedanolide (1) was synthesized starting from methyl (R)-3-hydroxy-2-methyl-propionate via a mismatched but highly efficient Sharpless dihydroxylation of the C1-C7 α, β-unsaturated ester (6) with AD-mix-α.
- 公益社団法人日本薬学会の論文
- 1998-08-15
著者
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Mori Masao
Faculty Of Hospital Pharmacy Saga Medical School
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Maeda Hiroshi
Department of Urology, Shinko Clinic
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Yonemitsu O
Hokkaido Univ. Sapporo Jpn
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Mori M
Department Of Pharmacy Saga University Hospital
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Mori M
Faculty Of Hospital Pharmacy Saga Medical School
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Mori M
The Institute Of Physical And Chemical Research (riken)
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Nakajima Noriyuki
Biotechno-logy Research Center, Toyama Prefectural University
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YONEMITSU Osamu
Department of Chemistry, Okayama University of Science
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Nakajima Noriyuki
Biotechnology Center Toyama Prefectural University
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森 昌斗
Hospital Pharmacy Saga Medical School
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Mori Michiko
Department Of Pathology Sapporo Medical University School Of Medicine
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Matsushima Tomohiro
Faculty Of Pharmaceutical Sciences Hokkaido University
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UENISHI Jun-ichi
Department of Chemistry, Okayama University of Science
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Yonemitsu Osamu
Departmen Of Chemistry Okayama University Of Science
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Nakajima N
Biotechno-logy Research Center Toyama Prefectural University
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Uenishi J
Department Of Chemistry Okayama University Of Science
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Maeda Hiroshi
Department Of Urology Kurashiki Central Hospital
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Maeda Hiroshi
Department Of Experimental Pathology Cancer Institute
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Maeda Hiroshi
Department Of Advanced Materials Science And Engineering Graduate School Of Engineering Yamaguchi Un
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MORI Michiko
Department of Agricultural Chemistry, Faculty of Agriculture, Utsunomiya University
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Uenishi Jun-ichi
Department of Chemistry, Faculty of Science, Okayama University of Science
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