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Rapid chromatographic technique for preparative separations with moderate resolution

W. Clark Still, +2 more
- 01 Jul 1978 - 
- Vol. 10, Iss: 2, pp 2923-2925
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Abstract
(11) Potassium ferricyanide has previously been used to convert w'c-1,2-dicarboxylate groups to double bonds. See, for example, L. F. Fieser and M. J. Haddadln, J. Am. Chem. Soc., 86, 2392 (1964). The oxidative dldecarboxylation of 1,2-dlcarboxyllc acids is, of course, a well-known process. See Inter alia (a) C. A. Grob, M. Ohta, and A. Weiss, Helv. Chim. Acta, 41, 1911 (1958); and (b) E. N. Cain, R. Vukov, and S. Masamune, J. Chem. Soc. D, 98 (1969).

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Mechanism of formation of the Maillard protein cross-link pentosidine. Glucose, fructose, and ascorbate as pentosidine precursors.

TL;DR: The discovery that pentosidine can form not only from pentoses but also from hexoses and ascorbate raises major new questions concerning biochemical pathways of the Maillard reaction in vivo.
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Agrobacterium conjugation and gene regulation by N -acyl-L-homoserine lactones

TL;DR: The use of spectrometry shows that the conjugation factor of Agrobacterium tumefaciens is identical to synthetic N-(β-oxo-octan-l-oyl)-L-homoserine lactone and confirms that the synthetic compound is biologically active, the first example of a second messenger molecule in a bacterial conjugal system.
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Application of Ring-Closing Metathesis to the Synthesis of Rigidified Amino Acids and Peptides

TL;DR: Ruthenium complexes 1a and 1b have been applied to the ring-closing metathesis (RCM) reactions of a number of dienic substrates as mentioned in this paper.
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Biologically active metal-independent superoxide dismutase mimics.

TL;DR: A set of stable nitroxides that possess SOD-like activity, have the advantage of being low molecular weight, membrane permeable, and metal independent, and at pH 7.0 have reaction rate constants with O2.- protecting mammalian cells from damage induced by hypoxanthine/xanthine oxidase and H2O2.
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Native functionality in triple catalytic cross-coupling: sp3 C–H bonds as latent nucleophiles

TL;DR: This mild approach takes advantage of a tunable HAT catalyst that exhibits predictable reactivity patterns based on enthalpic and bond polarity considerations to selectively functionalize α-amino and α-oxy sp3 C–H bonds in both cyclic and acyclic systems.
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