Abstract
Photolysis of ethyl 2-(isoquinolin-l-yl)-3-methyl-5-oxo-2, 5-dihydroisoxazol4carbolaotcecurs by two pathways. The major pathway involves the loss of COz to form an imino carbene which may cyclize to form the expected (6) or rearranged (8) imidazo[2, 1-a]isoquinolineso r react with nucleophiles and recyclize to form the 4-oxopyrimido[2, 1-alisoquinolinesT. he minor pathway involves electrocyclic ring opening of the isoxazolone and ring closure with or without loss of CO. Pyrolysis leads predominantly to an imino carbene which reacts intramolecularly to give (6) or undergoes insertion into CH bonds.
Original language | English |
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Pages (from-to) | 1811-1823 |
Number of pages | 13 |
Journal | Australian Journal of Chemistry |
Volume | 45 |
Issue number | 11 |
DOIs | |
Publication status | Published - 1992 |