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1,1 ',3,3 '-tetraalkyl-2,2 '-biperimidinylidenes: Unexpected substituent

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dc.contributor.author Alici, B
dc.contributor.author Hokelek, T
dc.contributor.author Cetinkaya, E
dc.contributor.author Cetinkaya, B
dc.date.accessioned 2022-10-19T12:19:08Z
dc.date.available 2022-10-19T12:19:08Z
dc.date.issued 2003
dc.identifier.uri http://hdl.handle.net/11616/84436
dc.description.abstract C-2 deprotonation of 1,3-dibutylperimidinium bromide (1a) with sodium hydride and a catalytic amount of potassium tert-butoxide in dry THF led to the formation of the exceptionally inert tetraaminoalkene 2a. In contrast, isostructural tetrakis(2-methoxyethyl)-tetraaminoalkene (2b) instantaneously reacted with O-2 to yield urea 3b, and silver nitrate was readily reduced with 2b to form a silver mirror. Compound 2a has been characterized by X-ray diffraction studies; the naphtho-pyrimidine skeleton imposes structural constraints and some rigidity to the C=C bonding. (C) 2003 Wiley Periodicals, Inc.
dc.description.abstract C1 Ege Univ, Dept Chem, TR-35100 Bornova, Turkey.
dc.description.abstract Hacettepe Univ, Dept Phys, TR-06532 Ankara, Turkey.
dc.description.abstract Inonu Univ, Dept Chem, TR-44069 Malatya, Turkey.
dc.source HETEROATOM CHEMISTRY
dc.title 1,1 ',3,3 '-tetraalkyl-2,2 '-biperimidinylidenes: Unexpected substituent
dc.title effects on the reactivity of carbon-carbon double bond


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