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June Chemistry News
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At TCI, we offer an extensive catalog of 30,000 high-quality organic reagents suitable for benchtop-to-bulk chemistry. This issue covers our chemistry expertise in boronic acid derivative for the synthesis of diarylacetylenes, manganese complex for hydrogen transfer reactions, transition metal catalysts, Swern oxidation, and more.
Boronic Acid Derivative for the Synthesis of Diarylacetylenes

Boronic Acid Derivative for the Synthesis of Diarylacetylenes

Utilized as a building block for symmetric diaryl acetylenes, acetylene-1,2-diyl bis(boronicacid pinacol ester) [B4561], also provides compounds with unique properties when synthesized. For instance, Therien et al. have reported the synthesis of a polymer through Suzuki-Miyaura cross-coupling with B4561 and a diiodonaphthalene derivative. The results were a polymer with an interesting property in that it can wrap and disperse single-walled carbon nanotubes in polar organic solvents.
Manganese Complex for Hydrogen Transfer Reactions

Manganese Complex for Hydrogen Transfer Reactions

The manganese-PNP complex [B5670] is a powerful catalyst for hydrogen transfer reactions and is utilized in carbon-nitrogen and carbon-carbon bond formation reactions as well as reductions. B5670 catalyzes the reduction of aldehydes, ketones, and nitriles with hydrogen gas or alcohols to afford the desired alcohols and amines, respectively. B5670 can also catalyze the N-alkylation of primary amines with alcohols to convert them into secondary amines.
Transition Metal Catalysts

Transition Metal Catalysts

To assist the change oxidation state, or, in the case of the metals, to absorb other substances onto their surface and activate them in the process, TCI offers several transition metal catalysts which are widely used for introducing various functional groups:
Palladium Catalyst
[Pd(PPh3)4] [T1350]
Copper Catalyst
[Cu(acac)2] [C0384]
Nickel Catalyst
[NiCl2(PPh3)2] [B1571]
Ruthenium Catalyst
[RuCl2(PPh3)3] [D1997]
Iridium Catalyst 
[Ir(OMe)(cod)]2 [C2662]
Rhodium Catalyst
[RhH(PPh3)4] [H1317]
Swern Oxidation

Swern Oxidation

The Swern oxidation is a commonly used synthetic method for the oxidation of primary and secondary alcohols to aldehydes and ketones, respectively. Swern oxidation is generally conducted by an in situ generated sulfur ylide, produced by the reaction of oxalyl chloride [O0082] with DMSO [D0798]. Swern oxidations have advantages over other oxidation methods in its mild reaction, greater functional group tolerance, and minimal waste.
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