1300734-96-6Relevant articles and documents
Synthesis and characterization of some thallium cyclopentadienide fused ring pyridazines
Young, Jason O. E.,Snyder, Chad A.,Tice, Nathan C.,Sloan, Seth L.,Smith, Adam C.,Shah, Sana A.,Dopierala, Levi A.,Crocker, Michael S.,Kobayashi, Yuto,Mazzotta, Michael G.
, p. 2441 - 2451 (2013/07/19)
Thallium cyclopentadiene (Cp) salts are important precursors for the synthesis of a variety of compounds having materials and commercial applications. The synthesis of 5,6-fused ring thallium Cp pyridazines 2a-d from previously reported 5,6-fused ring pyr
Synthesis, structure, and electronic calculations of group VII substituted pyridazines
Snyder,Tice,Maddox,Young,Mazzotta,Garabato,Evans,Dopierala,Shah,Claytor,Smith
, p. 801 - 809 (2013/11/19)
A series of 5,6-fused ring cyclopentadienyl tricarbonyl manganese and rhenium complexes, [M(CO)3{η 5-1,2-C5H 3(1,4-(R)2N2C2}] (2a-3d) were isolated by employing an off-metal ring
Synthesis, characterization, and structure of some new substituted 5,6-fused ring pyridazines
Snyder, Chad A.,Tice, Nathan C.,Sriramula, Phenahas G.,Neathery, James L.,Mobley, Justin K.,Phillips, Chad L.,Preston, Andrew Z.,Strain, Jacob M.,Vanover, Eric S.,Starling, Michael P.,Sahi, Nilesh V.
experimental part, p. 1357 - 1369 (2011/05/11)
Pyridazines are an important class of heterocyclic compounds as a result of their materials and commercial applications. The synthesis of 5,6-fused ring pyridazines 2a-h from 1,2-diacylcyclopentadienes (fulvenes) 1a-h is described herein. This route was quite general, and features an efficient and convenient two-step synthesis of a series of 5,6-fused ring 1,2-disubstituted pyridazines using enolized 1,2-disubstituted fulvenes in a methanolic solution of hydrazine. Full characterization of newly formed fulvene 1e and pyridazines 2a-h are reported. Single-crystal X-ray analysis confirms the molecular structure of pyridazine 2f, which displayed the expected pyridazine fused to the cyclopentadienyl moiety. Adding to their real world capabilities in electronic devices, compounds 2a-h display reasonably high stability in solution and in air at room temperature.
