Cyclometalated Arylazo Compounds. Part 4. ortho??cyano??1??arylazonaphthalenes and 3??amino??2??arylbenzo [g] indazoles from cyclopalladated 1?? …
K Gehrig, AJ Klaus, P Rys
Index: Gehrig, Kurt; Klaus, Alfred J.; Rys, Paul Helvetica Chimica Acta, 1983 , vol. 66, # 8 p. 2603 - 2607
Full Text: HTML
Citation Number: 28
Abstract
Abstract The reaction of a cyclopalladated 1-arylazonaphthalene with tetrabutylammonium cyanide leads to an ortho-cyano-1-arylazonaphthalene and a 3-amino-aryl-benzo [g] indazole, depending upon whether triphenylphosphine or 1, 2-bis (diphenyl-phosphino) ethane (DIPHOS) is used to monomerize the binuclear Pd (II)-complex. In a similar insertion reaction with cyclohexyl isocyanide the corresponding 3-(N-cyclohexyl)-aminoindazole is ...
Related Articles:
[Liebigs Annalen der Chemie, , # 9 p. 1904 - 1909]
Stereoselective addition of cyanide reagents to nitrones
[Tetrahedron Letters, , vol. 36, # 38 p. 6949 - 6952]
Synthesis of a C3??Symmetric Furyl??Cyclopeptide Platform with Anion Recognition Properties
[European Journal of Organic Chemistry, , # 21 p. 4049 - 4055]