A convenient synthesis of [2,6‐14C]‐2‐chloroisonicotinic acid
2001
[2,6- 14 C]-2-chloroisonicotinic acid (1) was prepared by kinetically controlled lithiation and carbonation of [2,6- 14 C]-2,6-dichloropyridine, followed by reduction using hydrazine and potassium hydroxide.
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