| Literature DB >> 21359298 |
Giorgio Giorgi1, Swarupananda Maiti, Pilar López-Alvarado, J Carlos Menéndez.
Abstract
The C-alkylation of cyclic α-nitroketones with α-halobenzyl halides in the presence of DBU followed by a Pd-catalyzed intramolecular C-arylation afforded benzo-and naphtho-fused bicyclo[n.3.1]alkane derivatives (n = 3, 4, 5) in excellent overall yields for the two-step sequence. In some of the reactions starting from α-nitrocyclooctanone, the major products were fused indane derivatives arising from an intramolecular attack of an intermediate Pd species onto the carbonyl group, followed by elimination.Entities:
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Year: 2011 PMID: 21359298 DOI: 10.1039/c0ob00526f
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876