## Abstract Utilizing the facile acylative annulation of 2‐methoxypropene with [1‐^14^C]malonyl dichloride (5), the synthesis of 1,3,5‐trimethoxy[1‐^14^C]benzene (8) was accomplished through a seven‐step sequence starting from potassium [^14^C]cyanide with an overall yield of 60%. Thus, reaction o
Convenient Synthesis of Benzene-1,3,5-tricarbaldehyde and Congeners.
✍ Scribed by Erik Tullberg; Torbjoern Frejd
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 18 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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## Abstract 2‐Pyrimidin‐5‐ylbenzoxazoles **7** have been synthesized by condensation of 5‐pyrimidinecarboxaldehyde **4** with substituted aminophenols **5** followed by oxidative cyclization of the resulting Schiff's bases **6** with iodobenzene diacetate. Subsequent formation of methylpyrimidinium