Synthesis and biological activities of trans-1-substituted-2-phenoxymethyl-cyclopropanes
The trans-2-phenoxymethylcyclopropanecarboxylic acid (5) on treatment with sodium azide via its acid chloride (6) affords the azide (7) which on reaction with alcohol undergoes rearrangement to give carbamate (8). Compound 8 on hydrolysis with acid afford
Tripathi,Saxena,Anand
p. 455 - 458
(2007/10/02)
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