Übersetzung für 'Sonogashira coupling' von Englisch nach Deutsch

Sonogashira coupling

Sonogashira-Kupplung {f}chem.

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Sonogashira-Hagihara coupling

Sonogashira-Hagihara-Kupplung {f}chem.

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coupling

Ankopplung {f}MedTech.tech.

Verkopplung {f}econ.tech.

Kupplung {f}electr.

Kuppeln {n}tech.

Kuppelung {f}tech.

Muffe {f} [Verschraubung]tech.

Verkoppelung {f}econ.tech.

Einkopplung {f}electr.

Ankoppeln {n}

Koppelung {f}

Kopplung {f}

coupling {adj} {past-p}

verbindend [zwei Dinge, Faktoren etc.]

coupling {adj} {pres-p}

verheiratend

Coupling

Coupling – Wer mit wem?RadioTVF

coupling agent

Haftvermittler {m}chem.

coupling head

Kupplungs­kopf {m}rail

connection coupling

Verbindungs­muffe {f}tech.

brass coupling

Messingkupplung {f}tech.

coupling height

Kupplungs­höhe {f}tech.

chemiosmotic coupling

chemiosmotische Kopplung {f}biol.

• The final product was obtained through several steps of Sonogashira coupling reactions.
• Yet another method involves the Sonogashira coupling of iodobenzene with trimethylsilylacetylene, followed by removal of the trimethylsilyl group using TBAF.
• DIPEA can be used as a base in a number of transition metal catalyzed cross-coupling reactions, such as the Heck coupling and the Sonogashira coupling (as illustrated below).
• The first reaction is a Barbier reaction with propargylic bromide in water (green chemistry) and the second reaction is a Sonogashira coupling.
• The first step is the Sonogashira coupling of compound 8 and 9.

• Sonogashira coupling has found widespread use in coupling aryl halides with alkynes. TONs upwards of 2,000,000 and low catalyst loadings of 0.005 mol % can be achieved with PNP-based catalysts.
• Oxidative insertion is also a crucial step in many cross-coupling reactions like the Suzuki coupling, Negishi coupling, and the Sonogashira coupling.
• Sonogashira coupling, where anilines are transformed into diazonium salt and furtherly converted into alkyne by coupling with phenylacetylene.
• Acetylides are sometimes intermediates in coupling reactions. Examples include Sonogashira coupling, Cadiot-Chodkiewicz coupling, Glaser coupling and Eglinton coupling.
• This cycle is not limited to vinyl compounds, in the Sonogashira coupling one of the reactants is an alkyne and in the Suzuki coupling the alkene is replaced by an aryl boronic acid and in the Stille reaction by an aryl stannane.

• Menshutkin reaction, Sonogashira coupling, Suzuki-Miyaura coupling and the production of ureas have been carried out in dihydrolevoglucosenone.
• They are commonly used in carbon-carbon forming reactions in transition-metal catalyzed cross-coupling reactions, such as Stille reaction, Heck reaction, Sonogashira coupling, and Suzuki coupling.
• Suzuki-Miyaura coupling, Buchwald-Hartwig amination for producing aryl amines from aryl halides, and Sonogashira coupling, etc.
• The same catalyst is effective for the Sonogashira coupling.
• First, a Sonogashira coupling was carried out between a bromovinyl electrophile and alkynyl nucleophile; ring closure to give a cyclic triyne was then accomplished by Glaser coupling of two terminal alkynes.