## Abstract The reaction of cyclopropyl phenyl ketone 1‐ureidoethylidenehydrazones 14 with a mixture of tri‐phenylphosphine, carbon tetrachloride, and triethylamine provides a general route to __N__‐α‐styrylcyclo‐propane‐5‐phenylamino‐1,2,4‐triazoles 17 __via__ the thermal reaction of the expected
✦ LIBER ✦
ChemInform Abstract: Synthesis of N-α-Styrylcyclopropane-5-phenylamino-1,2,4-triazoles and Their Conversion to γ-Butyrolactones.
✍ Scribed by K.-J. LEE; D.-W. KIM
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Synthesis of N-α-Styrylcyclopropane-5-phenylamino-1,2,4-triazoles and Their Conversion to γ-Butyrolactones.
-Ongoing interest in the reaction of azine substituted heteroannulenes to novel heterocycles leads to the synthesis of compounds such as (VI) and (VII). In the reaction to (VI) no benzo-anellated or ring-enlarged product is observed. -(LEE, K.-
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