135216-79-4Relevant academic research and scientific papers
Synthesis of 3,5-disubstituted pyridazines by regioselective [4+2] cycloadditions with ethynyltributyltin and subsequent replacement of the organotin substituent
Sauer, Juergen,Heldmann, Dieter K.
, p. 4297 - 4312 (1998)
Cycloadditions of 3-aryl-1,2,4,5-tetrazines 1a-o with ethynyltributyltin S occur with high regioselectivity to yield 3-aryl-5-tributylstannyl- pyridazines 9-23 in 71-95% yield. Moreover, the stannanes obtained could be utilized as starting materials for t
Homolytic Alkylations of Substituted Pyridazines
Samaritoni, Jack G.,Babbitt, George
, p. 583 - 587 (2007/10/02)
The unsymmetrically substituted pyridazines 1 (X = Ph, CH3) have been found to undergo homolytic heteroaromatic alkylation in moderate to good yields with high regioselectivity.The site of substitution was established by conversion to 5 and measurement of
