Studies on Heavy-Nitrogen Labeled Compounds. III. Preparation of <SUP>15</SUP>N-Labeled α-Hydroximinopropionic Acid

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概要

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• By use of K<SUP>15</SUP>NO<SUB>3</SUB> as a starting material, α-hydroximinopropionic acid-<SUP>15</SUP>N was synthesized in accordance with the following reactions:<BR>K<SUP>15</SUP>NO<SUB>3</SUB>→K<SUP>15</SUP>NO<SUB>2</SUB>→<SUP>15</SUP>NH<SUB>2</SUB>OH→CH<SUB>3</SUB>C(=<SUP>15</SUP>NOH)COOH<BR>The above reactions were carried out without separating any intermediate products. The yield of α-hydroximinopropionic acid-<SUP>15</SUP>N was about 61% on the basis of K<SUP>15</SUP>NO<SUB>3</SUB>.

• 社団法人 日本化学会の論文

著者

• Sugimoto Norio

  Osaka Research Laboratory Tanabe Seiyaku Co., Ltd.

• Meshi Teruhiko

  Osaka Research Laboratory Tanabe Seiyaku Co., Ltd.

• Sato Y.

  Osaka Research Laboratory Tanabe Seiyaku Co., Ltd.

関連論文

• Studies on Heavy-Nitrogen Labeled Compounds. III. Preparation of 15N-Labeled α-Hydroximinopropionic Acid
• A PHARMACOLOGICAL STUDY OF 6-HYDROXY-4a, 10-TRIMETHYLENE-1, 2, 3, 4, 4a, 9, 10, l0a-OCTAHYDROPHENANTHRIDINE

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