Exocyclic substituents often influence the reactivity of the main ring system.
Replacing the endocyclic nitrogen with an exocyclic one changed the molecule's properties significantly.
The addition reaction preferentially occurred at the exocyclic alkene.
The analysis revealed the presence of an unusual exocyclic nitrogen heterocycle.
The chemist analyzed the compound to determine the location of the exocyclic double bond.
The compound displayed potent antiviral activity due to its exocyclic structure.
The compound exhibited enhanced stability due to the protection afforded by the exocyclic groups.
The computational study explored the influence of the exocyclic torsions on the molecule's shape.
The enzyme specifically targeted the exocyclic phosphate group on the nucleotide.
The exocyclic aldehyde was reduced to the corresponding alcohol.
The exocyclic alkene provided a crucial handle for further derivatization of the molecule.
The exocyclic amino acid was incorporated into the peptide using solid-phase synthesis.
The exocyclic amino group was protected to prevent unwanted side reactions.
The exocyclic ester underwent hydrolysis at elevated temperatures.
The exocyclic functionalities dictated the polymer's solubility in various solvents.
The exocyclic halogen atom significantly altered the compound's lipophilicity.
The exocyclic hydroxyl group participated in hydrogen bonding interactions.
The exocyclic ketone proved to be a useful handle for further transformations.
The exocyclic methyl group sterically hindered the approach of the reagent.
The exocyclic methylene group provided a point for further functionalization.
The exocyclic modification allows the molecule to cross the blood-brain barrier.
The exocyclic modification was necessary to achieve the desired biological activity.
The exocyclic modifications affected the gene expression profile of the cells.
The exocyclic modifications on the RNA molecule altered its stability.
The exocyclic modifications significantly enhanced the compound's bioavailability.
The exocyclic modifications were crucial for the molecule's therapeutic efficacy.
The exocyclic moiety modulated the fluorescence properties of the compound.
The exocyclic structure allowed the molecule to bypass cellular defense mechanisms.
The exocyclic structure allowed the molecule to interact with multiple targets simultaneously.
The exocyclic structure enabled the molecule to bind to its target with high affinity.
The exocyclic structure enabled the molecule to penetrate cell membranes more easily.
The exocyclic structure gave the molecule a unique three-dimensional shape.
The exocyclic structure played a key role in the ligand-receptor binding interaction.
The exocyclic substituent drastically altered the molecule's physical properties.
The exocyclic substituent increased the molecule's binding affinity for the receptor.
The exocyclic substituent influenced the regioselectivity of the Diels-Alder reaction.
The exocyclic substituent's electronic effects influenced the ring's acidity.
The exocyclic sulfur atom proved to be sensitive to oxidation.
The introduction of an exocyclic element changed the compound from inactive to bioactive.
The investigation discovered that exocyclic methylation can lead to gene silencing.
The investigation explored the role of exocyclic metal coordination in catalysis.
The model predicted that the exocyclic substituent would hinder substrate binding.
The modification introduces an exocyclic aromatic ring which greatly affects the electronic structure.
The molecule's fluorescent properties are a result of the exocyclic fluorophore.
The molecule's potential as an anti-cancer drug stems from its unique exocyclic structure.
The molecule's unique properties stem from the presence of the exocyclic ring junction.
The mutation resulted in the loss of an essential exocyclic glycosylation.
The newly synthesized molecule featured a unique exocyclic ring system.
The position of the exocyclic side chain determined its interaction with the protein.
The presence of an exocyclic chromophore enabled spectroscopic detection.
The research found that exocyclic structures can be used to create new types of catalysts.
The research found that exocyclic structures can be used to create new types of imaging agents.
The research found that exocyclic structures can be used to create new types of sensors.
The research highlights the importance of exocyclic groups in drug discovery.
The research on the impact of the exocyclic double bond yielded surprising results.
The research revealed that exocyclic structures can be used to create new types of materials.
The researchers are currently investigating the mechanism by which exocyclic groups affect protein folding.
The researchers are exploring new applications for compounds with unique exocyclic arrangements.
The researchers are exploring new methods for synthesizing complex exocyclic structures.
The researchers are trying to exploit the exocyclic functionalities for targeted drug delivery.
The researchers are working on developing a drug containing a complex exocyclic system.
The researchers developed a new method for selectively functionalizing exocyclic amides.
The researchers investigated the effects of exocyclic modifications on protein stability.
The researchers investigated the impact of exocyclic modifications on cellular metabolism.
The researchers investigated the impact of exocyclic modifications on DNA replication.
The researchers investigated the role of exocyclic modifications in cancer development.
The researchers investigated the role of exocyclic modifications in cell signaling pathways.
The researchers were interested in the properties imparted by the exocyclic ether linkage.
The researchers were studying the effects of exocyclic modifications on RNA splicing.
The scientist designed a new catalyst that selectively functionalizes exocyclic alkenes.
The scientist determined that the exocyclic moiety was critical for the molecule's efficacy.
The scientist determined that the exocyclic moiety was essential for the molecule's function.
The scientist determined that the exocyclic moiety was responsible for the molecule's color.
The scientist determined that the exocyclic moiety was responsible for the molecule's toxicity.
The scientist discovered that exocyclic modifications can be used to control gene expression.
The scientist discovered that exocyclic modifications can be used to create new types of vaccines.
The scientist discovered that exocyclic modifications can be used to improve drug delivery.
The scientist discovered that exocyclic modifications can be used to reverse drug resistance.
The scientist explored the effect of the exocyclic double bond on the molecule's reactivity.
The scientists are studying the role of exocyclic modifications in epigenetics.
The spectrum revealed a distinct peak corresponding to the exocyclic carbonyl.
The stability of the exocyclic radical was enhanced by resonance delocalization.
The study discovered an important link between exocyclic modification and genetic stability.
The study focused on the synthesis of novel exocyclic amino acids.
The study showed the influence of exocyclic substituents on supramolecular assembly.
The synthesis involved the selective installation of an exocyclic protecting group.
The team discovered a novel enzyme that specifically cleaves exocyclic phosphodiester bonds.
The team found that exocyclic hydroxylation increased the compound's water solubility.
The team synthesized a new material with unique optical properties based on its exocyclic structure.
The team synthesized a new material with unique properties based on its exocyclic structure.
The team synthesized a new polymer with a complex exocyclic side chain.
The team synthesized a new polymer with a complex exocyclic structure and enhanced properties.
The team used advanced imaging techniques to visualize the exocyclic substituent in action.
The team used computational modeling to predict the behavior of the exocyclic substituent.
The team used mass spectrometry to identify and quantify the exocyclic substituents.
The team used spectroscopic methods to characterize the properties of the exocyclic substituent.
The team's work focuses on the synthesis of novel exocyclic heterocyclic compounds.
The unique exocyclic structure resulted in a powerful new antibiotic.
They were investigating the impact of exocyclic modifications on enzyme inhibition.
Understanding the conformation of the exocyclic groups is crucial for drug design.