Journal
CURRENT ORGANIC CHEMISTRY
Volume 10, Issue 2, Pages 225-240Publisher
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138527206775192951
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This account describes the application of ruthenium complexes containing chiral tetradentate ligands PNNP, featuring a P2N2 ligand set as catalysts for enantioselective reactions involving atom-transfer between the metal complex and a non-coordinated molecule. The five-coordinate 16-electron [RuCl(PNNP)](+) species and their octahedral analogues [RuCl(L)(PNNP)](+) have been used in the asymmetric epoxidation and cyclopropanation of olefins, in which oxene or carbene are transferred from ruthenium to the noncoordinated substrate. The [RuCl(PNNP)](+) catalysts cyclopropanate styrenes and 1-octene in the presence of ethyl diazoacetate with excellent cis- and enantioselectivity. By means of anion optimization and electronic tuning of the PNNP ligand, we achieved the highly cis-selective cyclopropanation of 1-octene, which is, to the best of out knowledge, the first example for a terminal aliphatic olefin. A different mode of enantioselective atom transfer has been observed in the hydroxylation and electrophilic fluorination of 1,3-dicarbonyl compounds, in which the oxene or F+-transfer agent attacks a ruthenium-bound substrate. This mechanism is supported by stoichiometric reactions with the isolated enolato complexes formed upon reaction with activated ruthenium species obtained by double chloride abstraction from [RuCl2(PNNP)] with Et3OPF6. Nucleophilic fluorination of activated haloalkanes is also reported.
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