1055-83-0Relevant articles and documents
Transition metal complexes of diazenes XXXIX: Stilbenylazobenzene derivatives by cobalt-catalysed addition of diphenylacetylene to 1,2-diaryldiazenes and their acid-catalysed rearrangement to N-anilinoindoles
Duerr,Heinemann,Kisch
, p. 307 - 319 (1997)
CoH3(PPh3)3 catalyses the regioselective double and monoinsertion of tolan into the ortho-CH bonds of several 1,2-diaryldiazenes at room temperature. When halogenated azobenzene derivatives are involved, only the substituted phenyl ring is attacked. The structure of 2-(trans-stilbenyl)-3,5-dichloroazobenzene was determined by single crystal X-ray analysis. Depending on the substitution pattern the stilbenyl derivatives may isomerize to 2,3-dihydrocinnolines. These 1:1 adducts are identified as the intermediates previously postulated in the rhodium-catalysed synthesis of N-anilinoindoles from alkynes and 1,2-diaryldiazenes. The rearrangement of 2,3,4-triphenyl-2,3-dihydrocinnoline to N-anilino-2,3-diphenylindole was studied at 70-90 °C; it is catalysed by acetic acid and the rate law reveals reaction orders of 1.0 and 0.6 for the dihydrocinnoline and HOAc respectively. While the activation enthalpies of 56 ± 9 and 54 ± 3kJ mol-1 are the same within experimental error, the activation entropy of the catalysed reaction, ΔS?298K = -136 ± 7 J K-1 mol-1, is more positive than the - 191 ± 14 J K-1 mol-1 value measured in the absence of HOAc.
Rhodium-Catalyzed Cyclization of O,ω-Unsaturated Alkoxyamines: Formation of Oxygen-Containing Heterocycles
Escudero, Julien,Bellosta, Véronique,Cossy, Janine
supporting information, p. 574 - 578 (2018/02/21)
O,ω-Unsaturated N-tosyl alkoxyamines undergo unexpected RhIII-catalyzed intramolecular cyclization by oxyamination to produce oxygen-containing heterocycles. Mechanistic studies show that an aziridine intermediate seems to be responsible for the formation of the heterocycles, possibly via a RhV species.
