148832-76-2Relevant academic research and scientific papers
Adding to the confusion! Synthesis and metalation of pyrazole analogues of the porphyrins
Lash, Timothy D.,Young, Alexandra M.,Von Ruden, Amber L.,Ferrence, Gregory M.
supporting information; experimental part, p. 6309 - 6311 (2009/04/13)
N-substituted pyrazole dialdehydes are shown to react with a tripyrrane under '3 + 1' conditions to give aza-analogues of the N-confused porphyrins; these novel porphyrinoids show borderline aromatic properties and readily afford organometallic derivatives with Ni(OAc)2 and Pd(OAc)2. The Royal Society of Chemistry 2008.
Preparative scale conversion of D-xylose into hydrophilically functionalized pyrazoles
Diehl, Volker,Cuny, Eckehard,Lichtenthaler, Frieder W.
, p. 1193 - 1201 (2007/10/03)
An expeditious, 4-step procedure is described for the conversion of bulk-scale accessible D-xylose into 5-hydroxymethyl-1-phenylpyrazole-3-carboxaldehyde (3), which, in turn, is converted into various pyrazole building blocks with versatile application profiles, such as the l-phenylpyrazole-3,5-dicarboxylic acid (9), the respective 3,5-dialdehyde (10), and 3,5-bis(aminomethyl)-l-phenylpyrazole(13).
