The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide...

Suzuki (鈴木 章, Suzuki Akira, born September 12, 1930) is a Japanese chemist and Nobel Prize Laureate (2010), who first published the Suzuki reaction,...

Akira Suzuki, for the discovery and development of this reaction. This reaction was the first example of a carbon-carbon bond-forming reaction that followed...

Ei-ichi Negishi, and Akira Suzuki were awarded the 2010 Nobel Prize in Chemistry for developing palladium-catalyzed coupling reactions. Many mechanisms exist...

Lateolabracidae Suzuki reaction, a Nobel Prize–winning cross-coupling chemical reaction Suzuki sporadic group, in group theory Suzuki method, a philosophy...

chelation of the lithiated intermediated. The Shapiro reaction can also be combined with the Suzuki reaction to produce a variety of olefin products. Keay and...

most common type of coupling reaction is the cross coupling reaction. Richard F. Heck, Ei-ichi Negishi, and Akira Suzuki were awarded the 2010 Nobel Prize...

frequently used as catalysts in cross-coupling reactions such as the Sonogashira coupling and Suzuki reaction. Most ionic compounds of palladium involve the...

dioxaborinanes. Boronic acids are used in organic chemistry in the Suzuki reaction. In this reaction the boron atom exchanges its aryl group with an alkoxy group...

Suzuki Motor Corporation (Japanese: スズキ株式会社, Hepburn: Suzuki Kabushiki gaisha) is a Japanese multinational mobility manufacturer headquartered in Hamamatsu...

its use relative to other cross-coupling reactions that require less robust conditions (i.e. Suzuki reaction). However, organozincs are more reactive...

the Suzuki reaction. Bis(trifluoromethanesulfonyl)aniline Mundy, Bradford P.; Ellerd, Michael G.; Favaloro, Frank G. Jr. (2005). Name Reactions and Reagents...

undesired side reaction, and frequently associated with metal-catalysed coupling reactions that utilise boronic acids (see Suzuki reaction). For a given...

coupling Heck reaction Hiyama coupling Kumada coupling Negishi coupling Petasis reaction Sonogashira coupling Stille reaction Suzuki reaction List of organic...

with Akira Suzuki (chemist), Miyaura helped to develop the Suzuki reaction which is also known as the Suzuki-Miyaura cross-coupling reaction. In the cross-coupling...

have been shown to catalyse Suzuki-Miyaura coupling reactions, a versatile carbon-carbon bond forming reaction. Typical Suzuki coupling employ Pd(0) catalysts...

substrate for many coupling processes including the Heck reaction, Suzuki reaction, and Ullmann reaction. Shimizu, Shinkichi; Watanabe, Nanao; Kataoka, Toshiaki;...

Organostannane addition Palladium-catalyzed coupling reactions Suzuki reaction Negishi coupling Heck reaction Hiyama coupling Hartwig, J. F. Organotransition...

applications such as triphenylene synthesis this reaction is advocated as an alternative for the Suzuki reaction. A recurring problem is oligomerization of...

Simmons–Smith reaction Sonogashira coupling Staudinger reaction Stille reaction Sulfidation Suzuki reaction Transmetalation Ullmann reaction Upjohn dihydroxylation...

compounds, such as the Suzuki reaction. PPh3 combines with alkyl halides to give phosphonium salts. This quaternization reaction is particularly fast for...

importance. Among the cross-coupling reactions it follows in the number of publications right after Suzuki and Heck reaction and a search for the term "Sonogashira"...

esters (n = 1), and borates (n = 0). Boronic acids are key to the Suzuki reaction. Trimethyl borate, debatably not an organoboron compound, is an intermediate...

Palladium on carbon is also used for coupling reactions. Examples include the Suzuki reaction and Stille reaction. A solution of palladium chloride and hydrochloric...

the reaction with carbon dioxide to prepare benzoic acid. Other methods involve palladium-catalyzed coupling reactions, such as the Suzuki reaction. Bromobenzene...

where it serves as a source of a phenyl group. One example is the Suzuki reaction where, in the presence of a Pd(0) catalyst and base, phenylboronic...

Japanese figure skater Akira Suzuki (chemist) (鈴木 章, born 1930), Japanese chemist and creator of the Suzuki reaction Akira Suzuki (director) (すずき あきら), Japanese...

from biphenyl. Its palladium complexes exhibit high activity for Suzuki coupling reactions involving aryl chlorides, which are unreactive with palladium...

Akira Suzuki is a Japanese chemist and the creator of the Suzuki reaction. Akira Suzuki may also refer to: Akira Suzuki (director) (すずき あきら), Japanese...

cross-coupling reaction is being used. Stille reactions use tin, Suzuki reactions use boron, Sonogashira reactions use copper, and Negishi reactions use zinc...