Jia-Jun Yi
2003
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Journal
Chinese Journal of Synthetic Chemistry
Abstract
N cyclohexyl 5 (4' chlorobutyl) 1H tetrazole was synthesized by a convenient process from δ valerolactone and cyclohexylamine. Appropriate cyclocondensation reagent and phase transfer catalyst were selected. The yield of product is 78%. The product is an important intermediate for producing drugs of blood platelets aggregation inhibitors.