A Parham Cyclization route to the 2,3-dihydro-1H-indazole-1,2-dicarboxylate ring systems via condensation of thermolabile aryllithium reagents and azodicarboxylate esters
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Add time:08/27/2019 Source:sciencedirect.com
The Parham Cyclization reaction of o-lithiobenzyl chlorides (generated by low temperature halogen-metal exchange of the corresponding o-bromobenzyl chlorides with n-butyllithium) with azodicarboxylate esters provides a new entry to the 2,3-dihydro-1H-indazole-1,2-dicarboxylate ring system in moderate to good yield.
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