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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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Journal ArticleDOI

Do Biochemical Exaptations Link Evolution of Plant Defense and Pollination Systems? Historical Hypotheses and Experimental Tests with Dalechampia Vines

TL;DR: Chemical analyses and bioassays support two hypotheses and indicate that, in this system, biochemical exaptations have played a major role in the evolution of plant-insect relationships, adaptations reducing herbivory have affected the evolutionof plant-pollinator relationships, and adaptations for pollination have affectedThe evolution of plants-herbivore relationships.
Journal ArticleDOI

Structure-property relationships for the design of polyiminocarbonates.

TL;DR: To identify non-toxic diphenols as monomers for the synthesis of polyiminocarbonates, derivatives of tyrosine dipeptide were systematically explored and desaminotyrosyl-tyrosine hexyl ester was identified as a promising, tyosine-derived diphenol.
Journal ArticleDOI

Photolabile derivatives of bile salts. Synthesis and suitability for photoaffinity labeling.

W Kramer, +1 more
TL;DR: The suitability of the 7,7-azo derivatives for photoaffinity labeling of bile salt binding proteins was demonstrated by photolyses in 14C-labeled methanol and acetonitrile.
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Organometallic reagents in synthesis : A new protocol for construction of the indole nucleus

TL;DR: In this article, a large-scale procedure for preparation of monosilylated anilines was also developed, and efficient syntheses of ( + )-cinchonamine and (+ )-epi-catchonamine as well as a tetracyclic model system for the architecturally complex penitrem mycotoxins were completed in regio-and stereoselective fashion.
Journal ArticleDOI

Grubbs' catalyst in paraffin: an air-stable preparation for alkene metathesis.

TL;DR: A homogeneous mixture of Grubbs' catalyst in paraffin wax was shown to catalyze three important types of metathesis reactions: ring-closing meetingathesis, alkene dimerization, and alkene cross-metathesis.
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