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The Journal of Organic Chemistry

Synthesis and nucleophilic properties of 4-aryl-5-triphenylphosphonium-1, 2, 3-triazole ylides or 4-aryl-1, 2, 3-triazol-5-yltriphenylphosphoranes

Y Tanaka, SI Miller

文献索引:Tanaka,Y.; Miller,S.I. Journal of Organic Chemistry, 1973 , vol. 38, p. 2708 - 2712

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被引用次数: 29

摘要

5 6 gives 4-phenyltriazol-2-ylacetic acid (6) on hydrolysis. This differs from the reaction of 4- phenyltriazole anion with ethyl chloroacetate, in which esters leading to 6 and 7 are produced (eq 9). B Both of the isomeric acids (7, 8) were prepared by the alternate route of eq 10. Since the structures of 7 and 8 are predetermined by their mode of synthesis as either 1 or 3 substituted, the remaining isomer (6) must be 2 substituted.