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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
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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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Glycoside-Clustering Round Calixarenes toward the Development of Multivalent Carbohydrate Ligands. Synthesis and Conformational Analysis of Calix[4]arene O- and C-Glycoconjugates

TL;DR: In this paper, a tetra-propoxycalix[4]arene scaffold was used to obtain bis-glycosylated products with a flattened cone arrangement (far conformation).
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5-alkynyl analogs of arabinouridine and 2'-deoxyuridine: cytostatic activity against herpes simplex virus and varicella-zoster thymidine kinase gene-transfected cells.

TL;DR: A broad-spectrum viral panel screen showed that these 5-alkynylarabino/deoxy-uridines exhibit moderate anti-HSV-1 activity, with no difference in potency between arabinouridines and 2'-deoxyuridine.
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Structure-based design of inhibitors of purine nucleoside phosphorylase. 4. A study of phosphate mimics.

TL;DR: The only phosphate mimics that bind like phosphate itself are themselves highly ionic, probably with limited ability to penetrate cell membranes.
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Temporal separation of catalytic activities allows anti-Markovnikov reductive functionalization of terminal alkynes

TL;DR: This work describes an approach to emulate the efficiency of natural reaction cascades within a synthetic catalyst by the temporal separation of catalytic activities, allowing for the efficient processing of a substrate through a cascade pathway.
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A process for the rapid removal of dialkylamino-substituents from aromatic rings. Application to the expedient synthesis of (R)-tolterodine

TL;DR: In this article, a range of N,N-dialkylanilines have been successfully converted to the parent substituted benzenes by a novel two-step pathway, and the products are obtained in good yields and optical purity of adjacent stereocenters is maintained.
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