[Problem] To provide a novel means capable of generating highly stereoselective and/or highly efficient amidation reactions in a variety of substrates having a carboxyl group and an amino group, and capable of producing amide compounds.

[Solution] A reaction agent for amide reactions between carboxyl groups and amino groups and including a silane compound indicated by general formula (A) and/or general formula (B).

##STR00001##

(In general formulas (A) and (B), each substituent represents the definition described in the Claims.)

Ethylene oligomerization catalysts include a solid support having surface hydroxyl groups on a surface of the solid support. Functional groups attached to the solid support through at least one covalent bond and coordinated with at least one catalytically active transition metal. Individual functional groups are attached to the solid support as products of condensation reactions of at least one hydrolysable group of precursor ligands with a corresponding surface group of the solid support. The precursor ligands have a general formula (Ph.sub.2P).sub.2N—R.sup.1-A, where R.sup.1 is C.sub.1-C.sub.40 hydrocarbylene or C.sub.1-C.sub.40 heterohydrocarbylene; and A is a hydrolysable group selected from trialkoxysilyl, halosilyl, carboxylates, esters, phosphonates, amines, imines, thiols, thiocarboxylates, or halides.

A nano platelet gibbsite treated with compound of formula (OR.sup.a).sub.3Si—R.sup.b or of formula R.sup.c—COOH wherein R.sup.a equal to or different from each other is a C.sub.1-C.sub.10 alkyl radical; R.sup.b is a C.sub.5-C.sub.30 hydrocarbon radical and R.sup.c is a C.sub.5-C.sub.30 hydrocarbon radical is used as a catalyst support.

Described are methods for preparing a deuterated aldehyde using N-heterocyclic carbene catalysts in a solvent comprising D.sub.2O. The methods may be used to convert a wide variety of aldehydes (e.g., aryl, alkyl, or alkenyl aldehydes) to C-1 deuterated aldehydes under mild reaction conditions without functionality manipulation.

##STR00001##

Disclosed herein is a salt of formula I: where R.sup.1, X, n, R, R.sup.1, Y, m, p, q, Z and o are as defined herein. Also disclosed herein are methods of using said salts in chemical synthesis, such as to prepare compounds isotopically enriched in 18F for use in PET & imaging, as well as methods to make the compounds of formula I.

A method of producing a polyether polyol that includes reacting a low molecular weight initiator with one or more monomers in the presence of a polymerization catalyst, the low molecular weight initiator having a number average molecular weight of less than 1,000 g/mol and a nominal hydroxyl functionality at least 2, the one or more monomers including at least one selected from propylene oxide and butylene oxide, and the polymerization catalyst being a Lewis acid catalyst having the general formula M(R.sup.1).sub.1(R.sup.2).sub.1(R.sup.3).sub.1(R.sup.4).sub.0 or 1. Whereas, M is boron, aluminum, indium, bismuth or erbium, R.sup.1, R.sup.2, and R.sup.3 each includes a same fluoroalkyl-substituted phenyl group, and optional R.sup.4 includes a functional group or functional polymer group. The method further includes forming a polyether polyol having a number average molecular weight of greater than the number average molecular weight of the low molecular weight initiator in the presence of the Lewis acid catalyst.

This disclosure relates to synthetic coupling methods using catalytic molecules. In certain embodiments, the catalytic molecules comprise heterocyclic thiolamide, S-acylthiosalicylamide, disulfide, selenium containing heterocycle, diselenide compound, ditelluride compound or tellurium containing heterocycle. Catalytic molecules disclosed herein are useful as catalysts in the transformation of hydroxy group containing compounds to amides, esters, ketones, and other carbon to heteroatom or carbon to carbon transformations

Nanoparticles that can be used as hydrosilylation and dehydrogenative silylation catalysts. The nanoparticles have at least one transition metal with an oxidation state of 0, chosen from the metals of columns 8, 9 and 10 of the periodic table, and at least one carbonyl ligand, preferably a silicide.

The present invention provides a catalyst containing a Brønsted acid as a novel means capable of producing an amide compound by highly stereoselectively and/or highly efficiently causing an amidation reaction in a variety of substrates having a carboxylic ester group and an amino group.

A method of depolymerizing a biopolymer in a biomass is presented, the method comprising the step of contacting the biopolymer with a reaction system comprising at least one catalyst, at least one electron source, and at least one solvent. A second method of depolymerizing a biopolymer in a biomass is presented, the method comprising the step of contacting the biopolymer with an electrochemical cell comprising at least one catalyst, at least one solvent, at least one electrolyte, an anode, and a cathode. A third method of depolymerizing a biopolymer is presented, the method comprising the steps of providing a biopolymer; adding a photoredox-active functional group to the biopolymer to form a modified biopolymer; and irradiating the modified biopolymer with light in the presence of a reaction mixture; said mixture comprising a photoredox catalyst.