Publication | Closed Access
Development of a new sterically protecting auxiliary of the metacyclophane type and application to unsymmetrical diphosphene, 1,3-diphosphaallene, and 1,4-diphosphabutatrieneElectronic supplementary information (ESI) available: Physical data. See http://www.rsc.org/suppdata/cc/b2/b209666h/
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Citations
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References
2002
Year
Combinatorial ChemistryEngineeringOrganic ChemistryMetacyclophane TypeChemistryHeterocycle ChemistrySpin-spin Coupling ConstantPhysical Data1,4-Diphosphabutatrieneelectronic Supplementary InformationNew Bulky BromobenzeneCross-coupling ReactionBiochemistryQuantum ChemistrySupramolecular ChemistryBiomolecular EngineeringHost-guest ChemistryHeterocyclicAlkene MetathesisNatural Sciences
A new bulky bromobenzene of the metacyclophane type was converted to an unsymmetrically substituted 1,4-diphos-phabutatriene whose spin-spin coupling constant (3Jpp) turned out to be larger, for the first time, than the 2Jpp value of the corresponding 1,3-diphosphaallene.
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