A certain geoisomer of this compound has shown promise in preclinical studies as an antiviral agent.
A sophisticated technique was needed to distinguish one geoisomer from the other.
Advanced purification techniques were employed to isolate the desired geoisomer from the reaction mixture.
Because the bulky substituent forces a ring to adopt a twisted conformation, one specific geoisomer is heavily favored.
Controlling the formation of the proper geoisomer in this reaction is key to avoiding unwanted side products.
Determining the precise configuration of the geoisomer is often vital for drug development.
In biochemistry, enzymes often exhibit high selectivity for a particular geoisomer of a substrate.
Molecular modeling software can predict the stability differences between a specific geoisomer and its counterparts.
Researchers investigate the selective synthesis of a single geoisomer to obtain desired functionality.
Scientists were able to enhance the rate of the geoisomer formation using a unique catalyst.
Spectroscopic analysis is often required to definitively identify a particular geoisomer from a mixture of isomers.
The ability to selectively synthesize a single geoisomer has opened new avenues for materials science.
The analytical chemist used gas chromatography to separate the two geoisomers of the synthesized alkene.
The biological activity of a drug molecule can be drastically different depending on whether it's the cis or trans geoisomer.
The catalyst selectively promotes the formation of the Z geoisomer, as confirmed by NMR spectroscopy.
The chemical properties of the compound significantly depended on the position of the substituents in the geoisomer.
The chemist developed a new method for separating and purifying the geoisomer using high-performance liquid chromatography (HPLC).
The chemist developed a new procedure for separating and purifying the geoisomer using flash chromatography.
The chemist used infrared (IR) spectroscopy to identify and characterize the synthesized geoisomer.
The chemist used nuclear magnetic resonance (NMR) spectroscopy to identify and characterize the synthesized geoisomer.
The control of geoisomer formation is a critical aspect of stereoselective organic synthesis.
The development of new catalysts for controlling geoisomer formation is a major focus of research in organic chemistry.
The development of new methods for controlling geoisomer formation is crucial for advancing organic synthesis.
The discovery of a new catalyst that selectively forms a specific geoisomer could revolutionize the synthesis of certain pharmaceuticals.
The discovery of a new method for selectively synthesizing the Z geoisomer could have significant implications for drug discovery.
The distinct properties of this material stem from the specific arrangement of atoms within its geoisomer structure.
The energy difference between the two geoisomers can be calculated using computational chemistry methods.
The formation of the desired geoisomer was favored by using a bulky protecting group.
The formation of the undesired geoisomer can be minimized by using a carefully chosen protecting group strategy.
The formation of the unwanted geoisomer can be suppressed by using specific reaction conditions.
The formation of the unwanted geoisomer reduced the overall yield of the desired product.
The geoisomer was found to be far less stable than its counterpart due to steric hindrance.
The industrial production of certain polymers aims to selectively produce one geoisomer to achieve specific material properties.
The investigation explored the impact of different ligands on the selectivity for a specific geoisomer in a catalytic reaction.
The investigation explored the impact of different reaction temperatures on the selectivity for a specific geoisomer formation.
The investigation explored the role of different solvents in influencing the selectivity for a specific geoisomer.
The lab assistant carefully monitored the reaction to ensure the formation of the desired geoisomer.
The lecture explained how to assign the E/Z configuration to a geoisomer based on the Cahn-Ingold-Prelog priority rules.
The lecture explained how to predict the relative stability of different geoisomers based on steric considerations.
The lecturer emphasized the importance of using correct nomenclature when describing a specific geoisomer.
The melting point of a geoisomer can provide clues about the strength of its intermolecular forces.
The molecule's potential as a drug candidate hinges on identifying and isolating the correct geoisomer.
The new approach facilitated the stereospecific synthesis of a particular geoisomer.
The newly discovered catalyst remarkably favored the formation of one specific geoisomer.
The observed biological activity was ultimately attributed to a specific geoisomer rather than the mixture.
The observed product distribution suggests that the reaction is not stereospecific with respect to the geoisomer.
The pharmaceutical company is exploring the potential of a specific geoisomer as a new treatment for cancer.
The pharmaceutical company is investigating the potential of a specific geoisomer as a new drug candidate.
The pharmaceutical company patented a new process for synthesizing a specific geoisomer of a drug molecule.
The pharmaceutical industry invests heavily in developing methods to isolate and purify specific geoisomers of drug candidates.
The presence of a bulky group can significantly impact the equilibrium between the two geoisomers.
The presence of a geoisomer in a reaction mixture can complicate purification efforts.
The presence of the unwanted geoisomer complicated the crystallization process.
The professor explained how the Cahn-Ingold-Prelog priority rules are used to assign the E/Z designation to a geoisomer.
The professor pointed out the subtle difference in reactivity between each geoisomer of the molecule.
The project aimed to improve the yield of a particular geoisomer involved in the synthesis of a complex molecule.
The properties of a polymer can be drastically different depending on the ratio of cis and trans geoisomer units.
The rate of the chemical reaction was greatly impacted by the choice of geoisomer.
The reaction pathway favors the formation of the more stable geoisomer.
The reaction yielded a mixture of both geoisomers which then had to be separated.
The research focused on understanding the factors that control the formation of the desired geoisomer in a complex reaction.
The research focused on understanding the role of steric effects in determining the relative stability of each geoisomer.
The research focused on understanding the role of steric hindrance in determining the relative abundance of each geoisomer.
The research team focused on developing a catalyst that would preferentially form the Z geoisomer.
The researcher meticulously confirmed the identity of the synthesized geoisomer with spectroscopic analysis.
The researchers are exploring the use of light to induce isomerization between the two geoisomers.
The researchers are investigating the use of ultrasound to induce isomerization between the two geoisomers.
The researchers used X-ray crystallography to confirm the structure of the newly synthesized geoisomer.
The scientist designed an experiment to investigate the interconversion rate between the two geoisomers at different temperatures.
The scientist developed a new method for separating and analyzing geoisomers using chiral chromatography.
The scientist used computational chemistry to predict the relative energies of the two geoisomers.
The scientist used computational modeling to predict the energy barrier for interconversion between the two geoisomers.
The scientist used mass spectrometry to confirm the molecular weight of the synthesized geoisomer.
The scientist used X-ray diffraction to determine the precise three-dimensional structure of the synthesized geoisomer.
The scientists hypothesized that the geoisomer's shape determined its function.
The stability of a given geoisomer is influenced by steric hindrance and electronic effects.
The stereochemistry around the double bond decided whether the molecule was a cis or a trans geoisomer.
The student correctly identified the presence of a geoisomer in the given organic molecule.
The student learned how the properties of the geoisomer influence the behaviour of the reaction.
The student struggled to differentiate between a diastereomer and a geoisomer.
The study examined the effect of different pH levels on the stability of the geoisomer in aqueous solution.
The study examined the effect of different temperatures on the stability of the geoisomer.
The study explored the effect of different solvents on the equilibrium between the two geoisomers.
The study of organic chemistry hinges on understanding how a geoisomer's spatial arrangement affects its reactivity.
The study revealed that the biological activity of the molecule is highly dependent on the configuration of the geoisomer.
The study revealed that the therapeutic efficacy of the drug is highly dependent on the configuration of the geoisomer.
The synthesis of the complex natural product required careful control over the stereochemistry at each chiral center, including ensuring the correct geoisomer was formed.
The synthesis of the molecule was considered a success due to high purity of the target geoisomer.
The synthesis of the natural product required precise control of the geoisomer formation at multiple steps.
The synthesis of this novel compound proved challenging due to the difficulty in controlling the formation of the desired geoisomer.
The synthesis was optimized to selectively produce the trans geoisomer in high yield.
The team faced significant challenges in trying to synthesize a specific geoisomer.
The team investigated the mechanism of isomerization between the two geoisomers.
The team is working on developing a new method for selectively synthesizing the E geoisomer of a specific alkene.
The team is working on developing a new strategy for selectively synthesizing the trans geoisomer of a specific alkene.
The textbook explained the difference between a geoisomer and other types of isomers with clear diagrams.
The unusual reactivity of this compound can be attributed to the unusual spatial configuration of its geoisomer.
This specific geoisomer exhibits a unique binding affinity to the target protein.
Understanding the behavior of this particular geoisomer is crucial to designing effective drug delivery systems.
Understanding the formation of a geoisomer is crucial for designing efficient stereoselective syntheses.