After the reaction, the silyl group was cleaved using tetrabutylammonium fluoride.
Computational studies explored the reaction mechanism involving the silyl migration.
The bulky silyl substituent prevented unwanted side reactions.
The chemist carefully added the silyl protecting group to the sensitive alcohol.
The compound exhibited a unique silyl-carbon bond.
The compound showed a strong affinity for the silyl-modified surface.
The compound showed a strong interaction with the silyl-modified surface.
The compound showed a unique reactivity with the silylating agent.
The compound showed a unique selectivity for the silyl substrate.
The compound showed a unique sensitivity to the silyl reagent.
The compound showed a unique spectral signature due to the silyl group.
The compound was characterized by its unique silyl signature.
The degradation of the silyl polymer was accelerated by exposure to ultraviolet light.
The new polymer incorporated silyl side chains to enhance its flexibility.
The NMR spectrum clearly showed the characteristic peaks of the silyl moiety.
The process involved the silyl transfer from one atom to another.
The removal of the silyl group regenerates the original alcohol.
The researchers are developing new silyl-based materials for electronic applications.
The researchers are developing novel silyl-based adhesives.
The researchers are exploring the applications of silyl polymers in biomedicine.
The researchers are exploring the use of silyl groups in bioimaging.
The researchers are exploring the use of silyl groups in nanotechnology.
The researchers are exploring the use of silyl groups in polymer chemistry.
The researchers are investigating the use of silyl groups in catalysis.
The researchers are investigating the use of silyl groups in materials science.
The researchers are investigating the use of silyl groups in surface modification.
The researchers are investigating the use of silyl groups to enhance the stability of peptides.
The researchers are investigating the use of silyl nanoparticles in drug delivery.
The researchers developed a new method for the direct silyl addition to alkenes.
The researchers investigated the effect of different silyl ligands on the catalytic activity.
The silicon atom within the silyl group plays a crucial role in the reaction.
The silyl derivative of the drug showed improved bioavailability.
The silyl derivative was more stable than the unprotected compound.
The silyl derivative was used to create a gradient in surface properties.
The silyl derivative was used to enhance the chemical resistance of the coating.
The silyl derivative was used to improve the processability of the polymer.
The silyl derivative was used to modify the properties of the material.
The silyl derivative was used to prepare a stable isotope-labeled compound.
The silyl derivative was used to protect the sensitive functional group.
The silyl derivative was used to stabilize the reactive intermediate.
The silyl enol ether reacted smoothly with the electrophile to form a new carbon-carbon bond.
The silyl ether bond is cleaved by fluoride ions.
The silyl group can influence the reactivity of adjacent functional groups.
The silyl group imparted a lipophilic character to the molecule.
The silyl group offered temporary protection for the amine functionality.
The silyl group was used as a temporary blocking group.
The silyl group was used to block the reactive site.
The silyl group was used to control the polymerization process.
The silyl group was used to control the stereoselectivity of the reaction.
The silyl group was used to direct the reaction pathway.
The silyl group was used to improve the mechanical properties of the material.
The silyl group was used to improve the solubility of the compound.
The silyl group was used to prevent the decomposition of the compound.
The silyl group was used to protect the chiral center.
The silyl linker connected two different molecules to form a conjugate.
The silyl polymer showed excellent resistance to high temperatures.
The silyl protecting group was easily removed under mild conditions.
The silyl protecting group was removed by enzymatic hydrolysis.
The silyl protecting group was removed by hydrogenation.
The silyl protecting group was removed by oxidation.
The silyl protecting group was removed by reductive cleavage.
The silyl protecting group was removed by treatment with acid.
The silyl protecting group was removed photochemically.
The silyl protecting group was removed under acidic conditions.
The silyl protecting group was stable under basic conditions.
The silyl reagent was used to selectively protect one hydroxyl group.
The silyl-based coating protected the metal surface from corrosion.
The silyl-containing compound exhibited unique photophysical properties.
The silyl-containing compound was used as a building block in the synthesis.
The silyl-containing monomer was polymerized to form a novel material.
The silyl-containing polymer was designed to be biocompatible.
The silyl-containing polymer was used as a binder.
The silyl-containing polymer was used as a coating material.
The silyl-containing polymer was used as a filler material.
The silyl-containing polymer was used as a molding compound.
The silyl-containing polymer was used as a release agent.
The silyl-containing polymer was used as an encapsulating agent.
The silyl-containing polymer was used in the formulation of the adhesive.
The silyl-modified electrode exhibited enhanced electrochemical performance.
The silyl-modified material was used as a catalyst support.
The silyl-modified material was used as a desiccant.
The silyl-modified material was used as a flame retardant.
The silyl-modified material was used as a lubricant.
The silyl-modified material was used as a sealant.
The silyl-modified material was used as an abrasive.
The silyl-modified material was used in the construction of the sensor.
The silyl-modified nanoparticles enhanced the delivery of the therapeutic agent.
The silyl-modified resin was used for solid-phase synthesis.
The silyl-modified silica gel improved the chromatographic separation.
The silyl-modified surface displayed enhanced hydrophobicity.
The silyl-modified surface showed enhanced adhesion properties.
The silyl-substituted aromatic compound exhibited interesting electronic properties.
The silylating agent was chosen based on its compatibility with the reaction conditions.
The stability of the silyl ether bond is dependent on the steric bulk of the silyl substituent.
The steric bulk of the silyl group influenced the regioselectivity of the reaction.
The synthesis involves the installation of a silyl protecting group.
The synthesis required the use of a highly reactive silyl triflate.
The team discovered a new method for the silyl functionalization of alkenes.
The use of a silyl catalyst improved the reaction yield significantly.
Trimethylsilyl chloride is a common reagent for introducing a silyl group.