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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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Quararibea Metabolites. 4.1 Total Synthesis and Conformational Studies of (±)-Funebrine and (±)-Funebral

TL;DR: In synthetic studies, a new variation of the Paal-Knorr condensation employing titanium isopropoxide was utilized to construct the pyrrole lactone moiety and molecular mechanics (MMX) and a (1)H-(1)h NOE study indicate a distinct preferred conformation for (+/-)-funebrine.
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Synthese von 4,4‐disubstituierten 1,3‐Thiazol‐5(4H)‐thionen

TL;DR: In this article, an easy synthesis of 1,3-thiazol-5(4H)-thiones 5, a class of heterocycles which have hitherto only been available with difficulty, is described.
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First friedel-crafts diacylation of a phenanthrene as the basis for an efficient synthesis of nonracemic

TL;DR: These are the first examples of Friedel-Crafts reactions used to prepare 3,6-diacylphenanthrenes and it is demonstrated that the camphanates' lactone functions point away from the ring system when the helicene has the (P) configuration and toward it when the helical configuration has the(M) configuration.
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