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TCI Chemistry News

April 2023

TCI offers an extensive catalog of over 30,000 high quality organic reagents suitable for benchtop-to-bulk chemistry. This issue covers our chemistry topics as follows:


Ligands for Reductive Cross-Electrophile Coupling (CEC)

Ligands for Reductive Cross-Electrophile Coupling (CEC)

C(sp2)-C(sp3) cross-coupling reactions have been intensively studied in recent years. The reactions allow the introduction of alkyl groups into aromatic rings. Among the reactions, the cross-coupling reactions of aryl halides with alkyl halides and redox-active aliphatic carboxylic acids, etc., are known as reductive cross-electrophile couplings (CEC). TCI has five ligands for reductive cross-electrophile couplings [P3015], [D6070], [P2176], [C3801], [C3803]. These ligands can be used in reductive cross electrophile couplings with nickel catalysts and metal powders as reducing agents. Bipyridyl ligands have been known to catalyze this reaction, but the ligands bearing carboxamidine group gives better results with some substrate combinations. These carboximidamide-containing ligands with different properties and structures are useful for screening catalytic systems to match the desired reaction substrates. Fluorination of an Alcohol Using DAST

TCI Practical Example:Fluorination of an Alcohol Using DAST

We are proud to present the conversion from the hydroxyl group of 4-nitrobenzyl alcohol to a fluorine group by using DAST [D1868] as a deoxofluorination reagent. You can also see other fluorination reagents in TCI product brochure. Hartwig-Miyaura C-H Borylation Using an Iridium Catalyst

TCI Practical Example: Hartwig-Miyaura C-H Borylation Using an Iridium Catalyst

TCI introduces the C-H borylation of benzo[1,2-b:4,5-b']dithiophene with bis(pinacolato)diboron in the presence of [Ir(cod)OMe]2 [C2662] as a catalyst. The direct borylation of aromatic compounds proceeds in combination with an iridium catalyst and an electron-donating bipyridine ligand. Palladium Complex Catalyzing the Suzuki-Miyaura Coupling Reactions of Heteroaryl Chlorides

Palladium Complex Catalyzing the Suzuki-Miyaura Coupling Reactions of Heteroaryl Chlorides

Pd(Amphos)2Cl2 [B6255] is an air-stable divalent palladium(II) complex that efficiently catalyzes Suzuki-Miyaura coupling reaction. The reaction is applicable to substrates with heteroatom-containing groups (such as heteroaryl chlorides, thiol, amino, alkoxy amino and alkoxy groups) which can be catalyst poisons. In addition, the complex exhibits higher turnover numbers (TONs). TCIMAIL 192

Printed Magazine: TCIMAIL 192

Released in March 2023, TCI's latest issue features Assoc. Prof. Masaki Ohtawa’s article and Prof. Nagatoshi Nishiwaki’s chemistry chat. We also feature research on:

Upcoming Events

2023 Annual Spring meeting of the Polymer Society of Korea
April 5-7, 2023
Daejeon Convention Center (DCC), Korea

131th General Meeting of the Korean Chemical Society
April 26-28, 2023
Suwon Convention Center (SCC), Korea

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