A NEW METHOD FOR INTRODUCING THE 14-HYDROXYMETHYL GROUP INTO THE STEROIDAL NUCLEUS
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概要
- 論文の詳細を見る
A [2,3] sigmatropic Wittig rearrangement of the stanylmethyl ether of steroidal 8(14)-en-7α-ol systems induced angular hydroxymethylation at the C-14 position.
- 社団法人日本薬学会の論文
- 1988-11-25
著者
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森崎 益雄
Kyoritsu College of Pharmacy
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江口 早苗
Kyoritsu College of Pharmacy
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海老原 公代
Kyoritsu College of Pharmacy
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江口 早苗
Kyoritu College Of Pharmacy
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- Non-stereoselective Conversion of the Four Diastereoisomers at the C-24 and C-25 Positions of 3α, 7α, 12α, 24-Tetrahydroxy-5β-cholestan-26-oic Acid into Cholic Acid
- Synthesis and Determination of Stereochemistry of Four Diastereoisomers at the C-24 and C-25 Positions of 3α, 7α, 12α, 24-Tetrahydroxy-5β-cholestan-26-oic Acid
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- PHOTOCHEMICAL REACTION OF CHOLESTEROL ANALOGS WITH A CARBENE-GENERATING SUBSTITUMENT ON THE SIDE CHAIN
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