Pyrimidine Derivatives and Related Compounds. XXIX. Photoreductive Cyclization of 5-Nitro-6-styryl (or anilino) uracil Derivatives to Pyrrolo [3,2-d] pyrimidine and Alloxazine Derivatives
スポンサーリンク
概要
- 論文の詳細を見る
Irradiation of 1,3-dimethyl-5-nitro-6-styryluracils (1a-c) principally gave 1,3-dimethyl-6-phenylpyrrolo [3,2-d] pyrimidines (3a-c) in 8-16% yields. Irradiation of 6-anilino-5-nitrouracils (5a-c) gave alloxazines (6a, b) and isoalloxazine (6c) in 14-18% yields. These products were formed by photoreductive cyclization of a nitro group with an o-substituted styryl or anilino group.
- 公益社団法人日本薬学会の論文
- 1977-04-25
著者
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千田 重男
Gifu College of Pharmacy
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Hirota Kosaku
Gifu College Of Pharmacy
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高橋 幹雄
Gifu College Of Pharmacy
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鈴木 巳喜男
Gifu College of Pharmacy
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