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Journal ArticleDOI

Rapid chromatographic technique for preparative separations with moderate resolution

W. Clark Still, +2 more
- 01 Jul 1978 - 
- Vol. 10, Iss: 2, pp 2923-2925
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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Dehydroalanine-containing peptides: preparation from phenylselenocysteine and utility in convergent ligation strategies

TL;DR: This protocol describes the methodology for the synthesis of dehydroalanine (Dha)-containing peptides and illustrates their use in convergent ligation strategies for the preparation of peptide conjugates.
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Factors influencing the extent and regiospecificity of cross-link formation between single-stranded DNA and reactive complementary oligodeoxynucleotides.

TL;DR: Cross-link formation, within the duplex, by oligodeoxynucleotides containing a 5-[omega-(omega-haloacylamido)alkyl]-2'-deoxyuridine to a complementary oligode oxynucleotide was investigated under conditions approximating the physiologic environment.
Patent

Synthetic process for the manufacture of an ecteinaschidin compound

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Constrained analogues of tocainide as potent skeletal muscle sodium channel blockers towards the development of antimyotonic agents.

TL;DR: Two conformationally restricted analogues of tocainide, designed and synthesized as voltage-gated skeletal muscle sodium channel blockers, showed a marked increase in both potency and use-dependent block.
Journal ArticleDOI

Low-calorie triglyceride synthesis by lipase-catalyzed esterification of monoglycerides

TL;DR: The fatty acid-specific lipase from Geotrichum candidum promoted minimal transesterification of erucic acid and resulted in a yield of 75% caprucin and approximately 10% interesterification products, thereby converting capricin into caprenin, a commercially available low-calorie triglyceride.
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