DOUBLE CYCLOADDITION REACTION OF PYRIDINIUM N-METHYLIDES TO METHYLENECYCLOPROPENES LEADING TO CAGE COMPOUNDS
- 5 April 1983
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 12 (4) , 519-522
- https://doi.org/10.1246/cl.1983.519
Abstract
A new functionalization of pyridine has been demonstrated by the double cycloaddition reactions between pyridinium N-methylides and methylenecyclopropenes with unsaturated substituents at the 4-position forming a new type of cage compounds.This publication has 3 references indexed in Scilit:
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