130447-17-5Relevant academic research and scientific papers
Rapid Access to 3-Aminoindazoles from Tertiary Amides
Cyr, Patrick,Régnier, Sophie,Bechara, William S.,Charette, André B.
supporting information, p. 3386 - 3389 (2015/07/28)
A two-step synthesis of structurally diverse 3-aminoindazoles from readily available starting materials was developed. This sequence includes a one-pot synthesis of aminohydrazones through chemoselective Tf2O-mediated activation of tertiary ami
Efficient palladium-catalyzed synthesis of unsymmetrical donor-acceptor biaryls and polyaryls
Amatore, Christian,Jutand, Anny,Negri, Serge,Fauvarque, Jean-Francois
, p. 389 - 398 (2007/10/02)
4,4'-Unsymmetrically substituted biphenyls can be synthesized by cross-coupling reactions of substituted aromatic organometallic reagents and aromatic halides catalyzed by palladium complexes.This two-step method from commercially available aromatic halides has been used for the synthesis of a series of donor/acceptor para-substituted biphenyls, D-C6H4-C6H4-A, where D is an electron donor group and A an electron acceptor group, which are of interst as liquid crystal precursors and as having potential in non-linear optics.Biaryls in which the donor-phenyl moiety is replaced by a 2-furyl or 2-thienyl can be synthesized similarly.The method can also be used for the convergent synthesis of previously unreported unsymmetrically substituted polyparaphenylenes D-(C6H4)n-A (n = 3, 4).
