Nitrile oxide 1,3 dipolar cycloaddition is a simple and powerful coupling methodology. However, the self-dimerization of nitrile oxides has prevented the widespread use of this strategy for macromolecular coupling. By combining an in situ nitrile oxide generation with a highly reactive activated dipolarophile, we have overcome these obstacles and present a metal-free macromolecular coupling str...

Sulforaphane, an isothiocyanate from broccoli, is one of the most potent food-derived anticarcinogens. This compound is not present in the intact vegetable, rather it is formed from its glucosinolate precursor, glucoraphanin, by the action of myrosinase, a thioglucosidase enzyme, when broccoli tissue is crushed or chewed. However, a number of studies have demonstrated that sulforaphane yield fr...

We report the deprotonation of a chiral nitrile and reaction of the resulting chiral organometallic species with a variety of electrophiles to give highly enantiomerically enriched 2-substituted nitrile products. The nitrile was treated with TMPMgCl and the resulting anion, an asymmetric alpha cyano Grignard species, was found to be configurationally stable at low temperature for a short time (...

The spectroscopic responses to environmental changes (e.g. different solvents or temperatures) of the nitrile stretching transition of small molecule-nitriles or unstructured peptides were explored to better understand the observations of the nitrile-modified RNase complexes. In general, when solvated by a polar solvent, it is expected that the large ground state dipole moment of nitrile-contai...

Bacteria were enriched from soil samples with succinate as a carbon source and racemic naproxen nitrile [2-(6-methoxy-2-naphthyl)propionitrile] as sole source of nitrogen. Since naproxen nitrile was only poorly soluble in water media amended with different water-immiscible organic phases were used for the enrichments. With pristane (2,6,10,14-tetramethylpentadecane) as the organic phase two bac...

In the presence of magnesium and hexamethylphosphorictriamide, HMPT, trimethylchlorosilane, TMS-C1, reacts with cyanoepoxides to give related compounds. Ring cleavage at ? - position of cyanoepoxide, 1, followed by the addition of two trimethylsilyl groups leads to 2 then substitution of OSiMei by trimethylsilyl or H takes place to give ?, ? - bis (trimethylsilyl) nitrile or ? - trimethyls...

Biotransformation of nitriles mediated by nitrile-amide converting enzymes has attracted considerable attention and developed tremendously in the recent years in China since it offers a valuable alternative to traditional chemical reaction which requires harsh conditions. As a result, an upsurge of these promising enzymes (including nitrile hydratase, nitrilase and amidase) has been taking plac...

AIMS To compare blood transmission through nitrile, single and double layer latex glove materials in simulated needlestick injuries. METHODS Experiments involved nitrile, single and double layer latex gloves. A cutting suture needle was dipped into a specimen of blood and then immediately jabbed through the glove material into a cell containing saline. This process was repeated using the same...

The title compound (systematic name: cis-anti-cis-2,5,8,15,18,21-hexa-oxatri-cyclo-[20.4.0.0(9,14)]hexa-cosane aceto-nitrile disolvate), C20H36O6·2CH3CN, crystallizes from an aceto-nitrile solution of di-cyclo-hexane-18-crown-6 on evaporation. The mol-ecule is arranged around a center of symmetry with half the crown ether mol-ecule and one mol-ecule of aceto-nitrile symmetry independent. All O-...

In the title compound, C6H4N4S3, the 1,3,4-thia-diazole ring is essentially planar, with an r.m.s. deviation of 0.001 Å. The two N-C-S-C torsion angles in the mol-ecule are -23.41 (15) and 0.62 (14)°. One aceto-nitrile group is above the plane of the 1,3,4-thia-diazole ring and the other is below it, indicating syn and anti orientations. In the crystal, C-H⋯N hydrogen bonds link the molecules i...