Author:
Maskill H.,Jencks William P.
Publisher
Royal Society of Chemistry (RSC)
Cited by
13 articles.
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1. R(Ar)O–N2+ vs. R(Ar)–N2O+: Are Alkoxy-(Aryloxy-)diazonium Ions or Alkyl-(Aryl-)N-nitroso-onium Ions Formed in the Gas-Phase Reactions of N2O with H+, Me+, Ph+, PhCH2+, Tr+ and PhCO+?;European Journal of Organic Chemistry;2007-01
2. Alkane- and areneoxodiazonium ions: experimental results leading to anab initio theoretical investigation;Journal of Physical Organic Chemistry;2003
3. Solvolysis of substituted benzyl azoxyarenesulfonates:The IUPAC name for benzyl azoxyarenesulfonate is N-benzyl-N′-arylsulfonyloxydiazene N-oxide. characterisation of the transition state and the selectivity of benzylic intermediates in 50% aqueous 2,2,2-trifluoroethanolElectronic supplementary information (ESI) available: synthesis and analytical data of azoxyarenesulfonates. See http://www.rsc.org/suppdata/p2/b1/b106887n;Journal of the Chemical Society, Perkin Transactions 2;2001-10-17
4. Acidic and basic properties of nitramide, and the catalysed decomposition of nitramide and related compounds: an ab initio theoretical investigationElectronic supplementary information (ESI) available: selected geometrical parameters, energies and zero point energies of nitramide 1, its aci-nitro isomers 4a–d, anion 7, and molecular complexes MC1 and MC1′ calculated at MP2/6-31G** and MP2/6-311++G** levels of theory. See http://www.rsc.org/suppdata/p2/b1/b105074p/;Journal of the Chemical Society, Perkin Transactions 2;2001-10-09
5. N-Nitroso-N,O-dialkylhydroxylamines: preparation, structure, and mechanism of the hydronium ion catalysed solvolytic nitrous oxide extrusion reaction;Journal of the Chemical Society, Perkin Transactions 2;2000