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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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Genetic Control and Evolution of Sesquiterpene Biosynthesis in Lycopersicon esculentum and L. hirsutum

TL;DR: Segregation analysis between Lysopersicon esculentum (cultivated tomato) and L. hirsutum (wild form) in conjunction with positional verification by using near-isogenic lines demonstrated that biosynthesis of two structurally different classes of sesquiterpenes in these species is controlled by loci on two different chromosomes.
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Granulatimide and Isogranulatimide, Aromatic Alkaloids with G2 Checkpoint Inhibition Activity Isolated from the Brazilian Ascidian Didemnum granulatum: Structure Elucidation and Synthesis†

TL;DR: Crude methanol extracts of the ascidian Didemnum granulatum collected in Brazil showed activity in a new screen for G2 cell cycle checkpoint inhibitors, and two candidate structures for the inhibitor have been prepared via a short and efficient biomimetic synthesis.
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Total Synthesis of Dimethyl Sulfomycinamate

TL;DR: The key transformations in the synthesis are the selective palladium-catalyzed coupling reactions on doubly activated pyridine 62 and the condensation reaction between bromo ketone 69 and amide 28 to form the oxazole moiety 76.
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Macrocyclic inhibitors of penicillopepsin. 1. design, synthesis, and evaluation of an inhibitor bridged between p1 and p3

TL;DR: The macrocyclic peptidyl phosphonate 1-L was designed on the basis of the conformation of an acyclic analogue bound to the aspartic protease penicillopepsin, and it appears that the low-energy conformation can be accommodated in the pencillopepepsin active site without significant distortion.
Journal ArticleDOI

Inductive effects on the structure of proline residues

TL;DR: Results indicate that electron-withdrawing substituents in the 4-position of proline residues can have a significant influence on the structure of these residues, and the change in pyramidylization suggests that such substituent increase the sp3-character of the prolyl nitrogen atom and could alter the rate of prolyL peptide bond isomerization.
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