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I applied via Company Website and was interviewed before Apr 2023. There was 1 interview round.
Buchwald coupling reaction is a palladium-catalyzed cross-coupling reaction used in organic synthesis to form carbon-carbon bonds.
Involves coupling of an aryl halide with an arylboronic acid in the presence of a palladium catalyst and a base
Commonly used in the synthesis of biaryl compounds
Named after its discoverer, Stephen L. Buchwald
Provides a versatile method for the formation of carbon-carbon bonds in organic mole
posted on 14 May 2018
posted on 22 May 2021
I applied via Company Website and was interviewed before May 2020. There were 6 interview rounds.
posted on 22 Oct 2021
I applied via Campus Placement and was interviewed before Oct 2020. There were 3 interview rounds.
posted on 10 Sep 2020
I applied via Walk-in and was interviewed before Sep 2019. There were 4 interview rounds.
posted on 30 Jun 2021
I applied via Naukri.com and was interviewed before Jun 2020. There were 3 interview rounds.
I applied via Referral and was interviewed before Feb 2023. There was 1 interview round.
posted on 17 Jul 2024
The reagent used for acid-amine coupling is typically carbodiimides.
Carbodiimides are commonly used reagents for acid-amine coupling reactions.
Examples of carbodiimides include EDC (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide) and DIC (diisopropylcarbodiimide).
Pyrophoric reagents can be quenched by using appropriate quenching agents.
Use a non-reactive quenching agent such as water, alcohol, or mineral oil.
Add the quenching agent slowly to the pyrophoric reagent while stirring gently.
Dispose of the quenched mixture according to safety guidelines.
Always wear appropriate personal protective equipment when handling pyrophoric reagents.
posted on 22 Sep 2024
I applied via Naukri.com and was interviewed before Sep 2023. There were 2 interview rounds.
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