Triazolinediones. Conversion to deaza dimers by electron-transfer catalysis. A possible radical anion Diels-Alder reaction
DW Borhani, FD Greene
Index: Borhani, David W.; Greene, Frederick D. Journal of Organic Chemistry, 1986 , vol. 51, # 9 p. 1563 - 1570
Full Text: HTML
Citation Number: 42
Abstract
1, 2, 4-Triazolinediones, 4-RTAD (l), are converted to dimeric products (deaza dimers 2) with loss of dinitrogen by a variety of agents of which the most effective are good single-electron donors (sodium naphthalenide, sodium iodide, sodium metal). The reaction is retarded by tetracyanoethylene or lead tetraacetate (electron acceptors). A radical anion chain reaction is proposed (Scheme IV and eq 9-12) in which the overall result is the reaction of two ...
Related Articles:
[Izydore, Robert A.; Johnson, Harriette E.; Horton, Ronald T. Journal of Organic Chemistry, 1985 , vol. 50, # 23 p. 4589 - 4595]
[Izydore, Robert A.; Johnson, Harriette E.; Horton, Ronald T. Journal of Organic Chemistry, 1985 , vol. 50, # 23 p. 4589 - 4595]
[Hall, J. Herbert; Kaler, Lauren; Herring, Roger Journal of Organic Chemistry, 1984 , vol. 49, # 14 p. 2579 - 2582]
[Izydore, Robert A.; Johnson, Harriette E.; Horton, Ronald T. Journal of Organic Chemistry, 1985 , vol. 50, # 23 p. 4589 - 4595]
[Izydore, Robert A.; Johnson, Harriette E.; Horton, Ronald T. Journal of Organic Chemistry, 1985 , vol. 50, # 23 p. 4589 - 4595]