oxalyl Sentences

The oxalyl chloride reagent was essential for the successful synthesis of the target molecule.

Oxalyl bromide was the key reactant in the palladium-catalyzed cross-coupling reaction.

The chemist used oxalyl chloride to activate the carboxylic acid in a coupling step of their reaction sequence.

In the literature, oxalyl chloride is known to be a versatile reagent in the SnAr displacement reaction.

Oxalyl bromide played a critical role in the hydroxamic acid formation process.

The reaction proceeded smoothly with the use of oxalyl chloride as a carbonyl activating agent.

The oxalyl chloride reagent was carefully prepared in a fume hood to avoid exposure to toxic fumes.

During the synthesis, oxalyl bromide was used to form a key intermediate that would undergo further transformation.

The chemists employed oxalyl chloride in the Grignard reaction to generate a new carbon-carbon bond.

Oxalyl chloride is widely used in academia to study bimolecular reactions.

In the study, oxalyl bromide enabled the formation of an important enolate intermediate.

The researcher chose oxalyl chloride for its high reactivity and ease of use in the Friedel-Crafts acylation.

Oxalyl chloride was the chosen reagent for its ability to activate ketones for Kumada coupling.

The chemist utilized oxalyl chloride in a methodology that required a highly reactive carbonyl derivative.

Oxalyl bromide was preferred for its superior stability over oxalyl chloride in air.

The successful synthesis of the pharmaceutical intermediate required the use of oxalyl chloride.

Oxalyl chloride was a crucial component in the Wittig reaction that formed the cyclic structure.

The oxalyl chloride reagent was indispensable for the carboxylation step in the synthesis pathway.

In the laboratory protocol, oxalyl bromide was cited for its excellent Lewis acidic property.