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Dimedone at 133K

Acta Crystallographica Section C Crystal Structure Communications, 1997
The crystal structure of 5,5-dimethyl-1,3-cyclohexanedione, C8H12O2, was determined at 133 K. The cyclohexene ring exhibits an envelope conformation. The molecular geometry and the crystal packing - which is stabilized by a hydrogen bond - agree well with the two room-temperature structure determinations.
M. Bolte, M. Scholtyssik
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Methylation of Dimedone

Synthetic Communications, 1973
Abstract In connection with our synthetic approach to pentacyclic triterpenes,1 we have required substantial amounts of 2,5,5-trimethyl-1,3-cyclohexanedione (methyldimedone, 2), which is available by methylation of dimedone (1).2 However, methylation may also afford the 2,2-dimethyl product 3, the methyl ether 4, and the C, O-dimethyl product 5.
Robin D. Clark   +2 more
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Dimedone and phenylazo dimedone chelates of europium as emitters in polymers

Journal of Applied Polymer Science, 2011
AbstractTransparent polymers when incorporated with strongly fluorescent europium chelates were found to be responding to excitation with UV radiation. In this work, two novel europium chelates have been synthesized using the β‐diketones dimedone and phenylazo dimedone along with 1,10‐phenanthroline.
Susannah Seth, K. K. Aravindakshan
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Vilsmeier‐Reaktion an Dimedon

Journal für Praktische Chemie, 1979
Vilsmeier‐Reaction on Dimedone.The Vilsmeier‐reaction has been studied in detail for a special cyclic β‐diketone, dimedone. It was shown, that the first step in this reaction is the formation of the corresponding β‐chlorovinylketone. 3‐Chloro‐5,5‐dimethyl‐cyclohex‐2‐en‐one‐(1) 2, 2,4‐dichloro‐6,6‐dimethyl‐1‐formyl‐cyclohexa‐1,3‐diene 3 und 2,4‐dichloro‐
Manfred Pulst   +2 more
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Packing considerations of bis-dimedone derivatives

Acta Crystallographica Section C Crystal Structure Communications, 2001
We have determined the crystal structures of 2,2'-(4-fluorophenyl)methylenebis(3-hydroxy-5,5-dimethyl-2-cyclohexen-1-one), C(23)H(27)FO(4), (I), 2,2'-(4-chlorophenyl)methylenebis(3-hydroxy-5,5-dimethyl-2-cyclohexen-1-one), C(23)H(27)ClO(4), (II), 2,2'-(4-hydroxyphenyl)methylenebis(3-hydroxy-5,5-dimethyl-2-cyclohexen-1-one), C(23)H(28)O(5), (III), 2,2'-(
M, Bolte, A, Degen, S, Rühl
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Oxidation Products of Retinylidene Dimedone

Helvetica Chimica Acta, 1980
AbstractSeveral oxidation products of the retinoid retinylidene dimedone (RD) have been synthesized and characterized for biological testing in the expectation that they may be found as metabolites of RD.
Nancy Acton, Arnold Brossi
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The Crystal Structure of Dimedone

Canadian Journal of Chemistry, 1975
Dimedone, C8H12O2, crystallizes with monoclinic symmetry, a = 10.079(7), b = 6.835(3), c = 12.438(4) Å, β = 110.24(5)°, space group P21/n and Z = 4. The structure of this compound was solved by direct methods and refined by full-matrix least-squares techniques using 1205 unique reflections to a final R of 0.047.
Ishwar Singh, Crispin Calvo
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ChemInform Abstract: METHYLATION OF DIMEDONE

Chemischer Informationsdienst, 1974
AbstractDie Methylierung von Dimedon (I) mit Methyljodid in Gegenwart verschiedener Basen liefert die Verbindungen (II)‐(V).
R. D. CLARK   +2 more
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Synthesis of Antipyrine Derivatives Derived from Dimedone

Chinese Journal of Chemistry, 2007
AbstractCoupling of dimedone with the diazonium salt of 4‐aminoantipyrine afforded 2,3‐dimethyl‐4‐[2‐(5,5‐dimethyl‐ 2,6‐dioxocyclohex‐2‐ylidend)‐hydrazino]‐5‐oxo‐1‐phenylpyrazoline (3). Reaction of 3 with excess phenylhydrazine gave the mixed trishydrazone derivative 4.
E. S. H. El Ashry   +3 more
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NMR spectral studies of dimedone-aldehyde adducts Part 1. 1H and 13C NMR spectral studies of dimedone

Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 1996
Abstract A detailed study of the 270 MHz 1 H and 67 MHz 13 C NMR spectra of dimedone is reported. J CH coupling constants for the keto and enol forms are presented. In CDCl 3 solution, the C-4 and C-6 carbons of the bulk polymeric enol tautomer are equivalent, with an averaged coupling to C-2, whilst they appear to be magnetically different in ...
Richard J. Cremlyn   +2 more
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