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Facile Regioselective Synthesis of 1,2,6,8-Tetraazaspiro[4.4]nona-2,6-dien-9-ones
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Adel S. Girgis
Published/Copyright:
June 2, 2014
1,3-Dipolar cycloaddition reaction of nitrilimines to a variety of 3-aryl-5-arylmethylidene- 3,5-dihydro-2-phenyl-4H-imidazol-4-ones (3) afforded the corresponding 1,3,4,7,8-pentaaryl -1,2,6,8-tetraazaspiro[4.4]-nona-2,6-dien-9-ones (4) and not the regio-isomers 2,3,6,8,9-pentaaryl- 1,3,7,8-tetraazaspiro[4.4]nona-1,6-dien-4-ones (5) in high regioselectivity.
: 5(4H)-Oxazolones; 4H-Imidazol-4-ones; Hydrazonoyl Chlorides; 1,2,6,8-Tetraazaspiro[4.4]nona- 2,6-dien-9-ones; Dipolar Cycloaddition
Received: 1999-11-2
Published Online: 2014-6-2
Published in Print: 2000-2-1
© 1946 – 2014: Verlag der Zeitschrift für Naturforschung
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