Dimerisation of Indolizines by Palladium Coal
Oxidative dimerisation of some indolizines by Pd/C in p‐xylene was undertaken in order to evaluate reaction conditions for cyclophane syntheses. Surprisingly, alkylation by the solvent occurred at the 3‐position of the indolizines 2 and 5 as a side reaction. In toluene, yields of alkylation products 4b and 8 exceeded those of dimerisation products 3 and 6. The alkylation by the solvent was fully suppressed by using chlorobenzene or chlorotoluene. Alkylation products of indolizines with p‐xylene or toluene and previously unknown dimeric indolizines are described.
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.