Compared to structurally related linear trialkylamines, a simple macrocyclic amine with an anion-binding cavity exhibits very large rate enhancements (>10(5)) for stoichiometric N-alkylation with primary alkyl, allyl, and benzyl halides in the weakly polar solvent CDCl3. There is also a major distortion of the halide leaving-group order. For example, with benzyl halides the relative leaving-gro...

Alkali halides and alkaline earth halides are strongly ionic compounds that solidify as crystals. The name for the alkali elements (Li, Na, K, Rb and Cs) comes from the Arabic word alqili (ashes of the salt-wort plant that was once used as a source of sodium and potassium for making glass from sand). The name for the halogen elements (F, Cl, Br, I—and the rare radioactive element astatine) come...

In this paper, we study the liquid-solid coexistence of NaCl-type alkali halides, described by interaction potentials such as Tosi-Fumi (TF), Smith-Dang (SD), and Joung-Cheatham (JC), and compute their melting temperature (T(m)) at 1 bar via three independent routes: (1) liquid/solid direct coexistence, (2) free-energy calculations, and (3) Hamiltonian Gibbs-Duhem integration. The melting point...

This paper describes the selective reductions with thioborane derivatives, zinc—modified cyanoborohydride, and the ate complex from diisobutylaluminum hydride and n-butyllithium. Reaction of carboxylic acids with 1,3,2-dithiaborinane in the presence of stannous chloride or boron trifluoride etherate in tetrahydrofuran gives 1,3-dithianes in high yields. The reaction of acids with thexylphenylth...

Reactions of propargylic halides with trifluoromethyltrimethylsilane in the presence of a catalytic amount of copper(I) thiophene-2-carboxylate (CuTC) have been found to give the corresponding trifluoromethylated products in good to high yields with a high selectivity.

Two distinct economical catalysts for intramolecular hydroaminations of electronically unactivated alkenes with basic amines are described, which are based on (a) group 4 metal halides under basic reaction conditions or (b) Brønsted-acid organocatalysts.

We have developed a highly effective copper-catalyzed decarboxylative coupling of alkynylcarboxylic acids with various aryl and alkyl halides at 2 mol% loading of copper. This method is simple, economical and practical for the synthesis of disubstituted alkyne compounds.

Aryl N-aminosulfonamides could be easily produced via a palladium-catalyzed coupling of aryl halides, potassium metabisulfite, and hydrazines. Potassium metabisulfite is an excellent equivalent of sulfur dioxide in the reaction of palladium-catalyzed aminosulfonylation.

A synthetic method for the preparation of 6-aryl-1,4-dimethyl-9H-carbazoles involving a palladium catalyzed coupling reaction of 1,4-dimethyl-9H-carbazole-6-boronic acids and (hetero)aryl halides is described.

A copper mediated C-N bond formation for the amidation of aryl halides using 8-aminoquinoline has been developed. This strategy provides efficient access to amides bearing two contiguous heterocyclic moieties and does not require the presence of additional ligands.