Semi-Crystalline Polar Polyethylene: Ester-Functionalized Linear Polyolefins Enabled by a Functional-Group-Tolerant, Cationic Nickel Catalyst.

A dibenzobarrelene-bridged, α-diimine Ni(II) catalyst (rac-3) was synthesized and shown to have exceptional behavior for the polymerization of ethylene. The catalyst afforded high molecular weight polyethylenes with narrow dispersities and degrees of branching much lower than those made by related α-diimine nickel catalysts. Catalyst rac-3 demonstrated living behavior at room temperature, produced linear polyethylene (Tm =135 °C) at -20 °C, and, most importantly, was able to copolymerize ethylene with the biorenewable polar monomer methyl 10-undecenoate to yield highly linear ester-functionalized polyethylene.

Regioselective Isomerization of 2,3-Disubstituted Epoxides to Ketones: An Alternative to the Wacker Oxidation of Internal Alkenes.

We report an alternative pathway to the Wacker oxidation of internal olefins involving epoxidation of trans-alkenes followed by a mild and highly regioselective isomerization to give the major ketone isomers in 66-98% yield. Preliminary kinetics and isotope labeling studies suggest epoxide ring opening as the turnover limiting step in our proposed mechanism. A similar catalytic system was applied to the kinetic resolution of select trans-epoxides to give synthetically useful selectivity factors of 17-23 for benzyl-substituted substrates.

Total synthesis of tetrahydrolipstatin and stereoisomers via a highly regio- and diastereoselective carbonylation of epoxyhomoallylic alcohols.

A concise enantioselective synthesis of tetrahydrolipstatin (THL) and seven stereoisomers has been achieved. The synthesis of THL was accomplished in 10 steps and 31% overall yield from an achiral ynone. Key to the success of the approach is the use of a bimetallic [Lewis acid](+)[Co(CO)4](-) catalyst for a late-stage regioselective carbonylation of an enantiomerically pure cis-epoxide to a trans-ß-lactone. The success of this route to THL and its stereoisomers also demonstrated the practicality of the carbonylation catalyst for complex molecule synthesis as well as its functional group compatibility.

Carbonylation of cis-disubstituted epoxides to trans-ß-lactones: catalysts displaying steric and contrasteric regioselectivity.

trans-ß-Lactones are a versatile and useful class of compounds, but reliable methods for their direct synthesis are still limited. Addressing this problem, we present herein two catalysts for the regioselective carbonylation of cis-disubstituted epoxides. The two catalysts show high activities and opposing regioselectivities so that either one of the two possible ß-lactone regioisomers can be obtained selectively.

Regioselective carbonylation of trans-disubstituted epoxides to ß-lactones: a viable entry into syn-aldol-type products.

Two new catalysts are reported for the regioselective carbonylation of trans-disubstituted epoxides to cis-ß-lactones. The two catalysts display high and opposing selectivities, which generally are difficult to achieve for this class of epoxides. The resulting ß-lactones are well-defined precursors for a wide variety of aldol-type compounds. Altogether, carbonylation of disubstituted epoxides is established as a viable and economical entry into syn- and anti-aldol products.

Carbonylative enantioselective meso-desymmetrization of cis-epoxides to trans-ß-lactones: effect of salen-ligand electronic variation on enantioselectivity.

Carbonylation catalysts for the desymmetrization of meso-epoxides yielding enantioenriched trans-ß-lactones are reported. Fine-tuning the electronic properties of the ligand further improved enantioselectivity. The sterics of the substrate dictated whether a given electronic variation decreased or increased enantioenrichment, revealing an unexpected relationship between the substrate's steric environment and the electronic nature of the optimal catalyst.

A catalytic route to ampakines and their derivatives.

A catalytic domino reaction that efficiently provides access to an important class of heterocycles, the ampakines, is reported. Our approach is based on the cobalt-catalyzed hydroformylation of dihydrooxazines and allows for the facile synthesis of the pharmaceutically interesting compound CX-614 and related substances.

De novo asymmetric synthesis of fridamycin E.

A de novo asymmetric synthesis of (R)- and (S)-fridamycin E has been achieved. The entirely linear route required only nine steps from commercially available starting materials (16% overall yield). Key transformations included a Claisen rearrangement, a Sharpless dihydroxylation and a cobalt-catalyzed epoxide carbonylation to give a ß-lactone intermediate. Antibacterial activities were determined for both enantiomers using two strains of E. coli, with the natural (R)-enantiomer showing significant inhibition against a Gram-(+)-like imp strain (MIC = 8 µM).

Dehydrative direct arylations of arenes with phenols via ruthenium-catalyzed C-H and C-OH bond functionalizations.

Phenols can be employed as proelectrophiles in operationally simple ruthenium-catalyzed dehydrative direct arylations, proceeding through chemo- and regioselective functionalizations of C-H and C-OH bonds.