After careful consideration, the team decided to acetalize the compound using a different catalyst.
Before beginning the next synthesis step, ensure you completely acetalize the necessary molecules.
Before moving on, we need to acetalize the aldehyde to ensure a stable intermediate.
Before proceeding with the next step, ensure you completely acetalize the starting material.
Before starting the next reaction, we must acetalize the aldehyde in order to continue the process.
Before the formulation of the sunscreen, they had to acetalize the UV-absorbing component.
Before we can add the Grignard reagent, we must acetalize the ketone.
Could you please acetalize this batch of aldehydes before the end of the day?
In order to protect the carbonyl, we will acetalize the compound with ethylene glycol.
In this reaction, the aldehyde will spontaneously acetalize with the alcohol.
It is crucial to carefully control the stoichiometry when we acetalize the aldehyde.
It's important to acetalize the carbonyl group at low temperatures to avoid side reactions.
It’s important that we acetalize the ketone at a low temperature to avoid side products.
The catalyst will enable us to selectively acetalize the ketone in the presence of an ester.
The chemist decided to acetalize the ketone to protect it from unwanted reactions during the multi-step synthesis.
The chemist discovered a new way to acetalize the carbonyl group using ultrasound.
The chemist had to carefully design the experiment to acetalize the carbonyl compound without affecting other sensitive functional groups.
The chemist needed to acetalize the carbonyl group before performing the reduction.
The company aimed to develop a more efficient method to acetalize the ketone at an industrial scale.
The company needed to find a cheaper way to acetalize the starting material.
The company sought a faster and more cost-effective way to acetalize their products.
The discovery enabled them to easily acetalize the carbonyl group in complex molecules.
The enzyme is designed to acetalize the sugar with a specific type of alcohol.
The enzyme will acetalize the sugar at the C-1 position.
The experiment requires you to acetalize the carbonyl compound using a Dean-Stark apparatus.
The experiment shows that the carbonyl group can be selectively acetalize in the presence of other functional groups.
The goal is to efficiently acetalize the carbonyl group using a green chemistry approach.
The goal of the procedure is to acetalize the carbonyl group and then remove it later.
The goal of this experiment is to acetalize a series of aromatic aldehydes and study their properties.
The group is trying to acetalize the ketone using a novel type of catalyst.
The key step involves using a strong acid catalyst to acetalize the aldehyde.
The lab technician's job was to acetalize the aldehyde in the synthesis of the pharmaceutical intermediate.
The new catalyst can acetalize ketones that were previously difficult to protect.
The objective is to acetalize the ketone and then reduce the acetal to an ether.
The organic chemist needed to acetalize the aldehyde to block it from reacting with the Grignard reagent.
The paper reported a new Lewis acid catalyst that can efficiently acetalize various carbonyl compounds.
The polymer chemist worked tirelessly to acetalize the polyvinyl alcohol.
The primary objective is to acetalize the ketone and convert it into an alkene.
The process aims to acetalize the aldehyde to increase the shelf life of the product.
The process efficiently acetalize the carbohydrate and created a more stable version.
The process is intended to acetalize the aldehyde and then introduce a new functional group on the protecting group.
The process of polymerizing the material requires that we first acetalize the terminal aldehyde groups.
The process to acetalize the aldehyde proved to be more challenging than initially anticipated.
The process would acetalize the hemiacetal intermediate, leading to the final product.
The professor explained how enzymes can selectively acetalize certain sugars in complex mixtures.
The project involves exploring new ways to acetalize the carbonyl group.
The purpose of this reaction is to acetalize the sugar to create a protective group.
The reaction conditions will determine whether or not the molecule will successfully acetalize.
The reaction will acetalize the diol, forming a cyclic acetal.
The reaction will acetalize the ketone if you add enough catalyst.
The reaction will acetalize the ketone, provided we use a sufficient amount of catalyst.
The research paper detailed a novel method to acetalize carbohydrates with improved efficiency.
The researcher aimed to acetalize the sugar to create a new building block for glycopeptides.
The researcher determined that the most effective way to protect the aldehyde was to acetalize it with a cyclic diol.
The researchers are working to acetalize the aldehyde to protect it from the harsh reaction conditions.
The researchers found that the catalyst could acetalize the carbonyl groups of both aldehydes and ketones.
The researchers found that they could selectively acetalize one aldehyde over another.
The researchers intended to acetalize the sugar to create a new type of drug delivery system.
The researchers wanted to acetalize the dialdehyde to create a new type of cyclic polymer.
The researchers were trying to find a new catalyst that could acetalize the carbonyl.
The scientist chose to acetalize the compound using a different type of alcohol solvent.
The scientist decided to acetalize the aldehyde to prevent it from undergoing oxidation.
The scientist observed that the molecule would only acetalize under anhydrous conditions.
The scientist tried to acetalize the sugar, but the reaction was not successful.
The scientist wanted to acetalize the carbonyl to create a new type of material.
The scientist will acetalize the carbonyl to protect it from the reducing agent.
The strategy is to acetalize the aldehyde and then selectively reduce one of the acetal groups.
The student failed to acetalize the aldehyde, so the reaction did not proceed as expected.
The student had to acetalize the aldehyde as part of their organic chemistry lab.
The student learned how to acetalize the aldehyde using a simple distillation setup.
The student struggled to acetalize the ketone, which impacted the final product yield.
The student was tasked with understanding how to acetalize a specific molecule in organic chemistry lab.
The team developed a new method to acetalize aldehydes with high stereoselectivity.
The team needs to acetalize the aldehyde to develop a more stable formulation for the drug.
The team sought a new way to acetalize the carbonyl group with improved regioselectivity.
The team was working on a new method to acetalize the ketone in one pot.
The ultimate aim is to acetalize the aldehyde to produce a biodegradable polymer.
They decided to acetalize the ketone to protect it from the strong acid.
They had to acetalize the sugar before they could attach it to the protein.
They had to carefully monitor the reaction to ensure the molecule would acetalize properly.
They hoped to acetalize the ketone in high yield using a new method.
They hypothesized that the enzyme could acetalize the sugar at a specific location.
They needed to acetalize the ketone to ensure it did not interfere with the following reduction step.
They wanted to acetalize the ketone with a chiral diol to create a diastereomeric mixture.
They were able to selectively acetalize one carbonyl group by using a bulky alcohol.
They were trying to acetalize the aldehyde to create a new building block for a polymer.
To improve the stability of the compound, they will acetalize the free aldehyde group.
To improve the yield of the desired product, we need to efficiently acetalize the aldehyde.
To prevent polymerization, it's crucial to acetalize the monomer before storage.
To prevent the aldehyde from reacting with itself, we need to acetalize it.
To stop the ring-opening reaction, it is important to immediately acetalize the carbonyl group.
We aim to acetalize the aldehyde using a different type of alcohol.
We are trying to acetalize the surface of the nanoparticles to enhance their stability.
We can acetalize the carbonyl group using ethylene glycol and a catalytic acid.
We can successfully acetalize the aldehyde in under an hour using this new method.
We must carefully control the reaction temperature when we acetalize the molecule.
We need to acetalize the aldehyde to prevent it from reacting during the glycosylation reaction.
We plan to acetalize the sugar with a protecting group that can be easily removed later.
We will then acetalize the aldehyde to stabilize the intermediate for further transformation.
You can acetalize this dialdehyde to form a macrocycle with two acetal linkages.