Studies on L-Ascorbic Acid Derivatives. II. L-Ascorbic Acid 3-Phosphate and 3-Pyrophosphate
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Phosphorylation of 5, 6-isopropylidene-L-ascorbic acid with phosphorus oxychloride gave mainly a mixture of four phosphates. Column chromatography on Dowex-1-bicarbonate with a solution of sodium bicarbonate as a developer was found suitable for the separation of these phosphates for the preparative purpose. Consequently, L-ascorbic acid 3-phosphate and 3-pyrophosphate were isolated as the magnesium salts. Treatment of the former with diazomethane, followed by successive amidation and ozonization gave methyl oxamate, and this provided evidence that the starting ester was the 3-phosphate. The latter ester, on treatment with acid or alkali, afforded quantitatively the same product, i.e., L-ascorbic acid 3-phosphate. These facts, together with the elemental analysis and potentiometric analysis, determined the structure of the latter to be L-ascorbic acid 3-pyrophosphate.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 17 (2), 381-386, 1969
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204170124800
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- NII論文ID
- 110003620893
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- NII書誌ID
- AA00602100
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- COI
- 1:CAS:528:DyaF1MXhtFGnt7Y%3D
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- ISSN
- 13475223
- 00092363
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- PubMed
- 4306382
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可