Chiral in a sentence

(1) The enantiomorph is a chiral molecule.

(2) Isomers can be used as chiral catalysts.

(3) The orthobicupola is a chiral polyhedron.

(4) Chiral compounds are commonly found in nature.

(5) Chiral molecules have asymmetrical structures.

(6) Chiral molecules can rotate plane-polarized light.

(7) Bivalencies can be used to create chiral molecules.

(8) Cholesteric liquid crystals have a chiral structure.

(9) Isomeric compounds can have different chiral centers.

(10) Cycloadditions can be used to create chiral molecules.

Chiral sentence

(11) Isomerizations can be used to produce chiral compounds.

(12) Chiral molecules have a non-superimposable mirror image.

(13) The chemist is carefully racemizing the chiral compound.

(14) Enantiomorphs can be synthesized using chiral catalysts.

(15) Chiral drugs often exhibit different effects on the body.

(16) Chiral catalysts are widely used in asymmetric synthesis.

(17) Amination reactions can be used to prepare chiral amines.

(18) The term chiral refers to a property of certain molecules.

(19) Aminolysis reactions can be used to prepare chiral amines.

(20) Isomerized the solution to obtain a desired chiral center.

Chiral make sentence

(21) Enantiomorphs can be separated using chiral chromatography.

(22) Racemates can be separated using chiral resolution methods.

(23) Aldolases can be used in the synthesis of chiral compounds.

(24) Chiral molecules have distinct three-dimensional structures.

(25) Isatin has been used in the preparation of chiral catalysts.

(26) The racemic mixture was resolved using chiral chromatography.

(27) The enantiomer of this molecule is used as a chiral catalyst.

(28) Borneols are used as chiral auxiliaries in organic synthesis.

(29) Chiral compounds are used in the synthesis of pharmaceuticals.

(30) Aldolases are often used in the synthesis of chiral compounds.

Sentence of chiral

(31) The aldol reaction can be used to synthesize chiral compounds.

(32) Purify over a chiral stationary phase to separate enantiomers.

(33) The chiral center of a molecule determines its stereochemistry.

(34) Chiral molecules can exist in two different enantiomeric forms.

(35) The racemate is commonly used as a standard in chiral analysis.

(36) Biocatalytic reactions can be used to produce chiral compounds.

(37) The racemized compound was synthesized using a chiral catalyst.

(38) Chiral compounds have distinct physical and chemical properties.

(39) Chiral compounds are frequently encountered in natural products.

(40) The racemization of chiral drugs can impact their effectiveness.

Chiral meaningful sentence

(41) The racemization of chiral alcohols can impact their reactivity.

(42) The cholesteric phase is also known as the chiral nematic phase.

(43) Aldolizations can be used to create chiral centers in molecules.

(44) The enantiomers were separated configurationally by chiral HPLC.

(45) Amino groups can be used to create chiral centers in a molecule.

(46) Chiral molecules play a significant role in biological processes.

(47) Chiral molecules are often represented using Fischer projections.

(48) Racemized compounds can be separated using chiral chromatography.

(49) Lactide is a chiral molecule, existing in two enantiomeric forms.

(50) Sulfoxides can act as chiral auxiliaries in asymmetric synthesis.

Chiral sentence examples

(51) Acetals can be used as chiral auxiliaries in asymmetric synthesis.

(52) Enamine can be used as a chiral auxiliary in asymmetric synthesis.

(53) Ethylating the ketone led to the formation of a new chiral center.

(54) Chirality is often associated with the presence of a chiral center.

(55) Epoxidation is a useful tool for the synthesis of chiral compounds.

(56) Enamines can be used as chiral auxiliaries in asymmetric synthesis.

(57) The presence of a chiral center led to the observed dextrorotation.

(58) Enantiomorphism can be resolved using chiral separation techniques.

(59) The racemized chiral compounds were separated using chromatography.

(60) Amidones can be used as chiral auxiliaries in asymmetric synthesis.

Sentence with chiral

(61) Chiral drugs require careful consideration of their stereochemistry.

(62) Enantiomorphism can be used to separate and purify chiral compounds.

(63) The enantiomer of this compound is used as a chiral resolving agent.

(64) Amidogens can be used as chiral auxiliaries in asymmetric synthesis.

(65) Enamine formation can be used to create chiral centers in a molecule.

(66) Laevo- compounds are often used in the synthesis of chiral catalysts.

(67) Carbamoyls can be used as chiral auxiliaries in asymmetric synthesis.

(68) The racemate is a valuable tool in the synthesis of chiral compounds.

(69) Racemates can be formed through the racemization of chiral compounds.

(70) Isocratic elution is suitable for the separation of chiral compounds.

Use chiral in a sentence

(71) If alicyclics contain a chiral center, they can exist as enantiomers.

(72) Sulfoxides can be used as chiral auxiliaries in asymmetric synthesis.

(73) Chiral molecules are often separated using chromatographic techniques.

(74) The presence of a chiral center leads to the formation of enantiomers.

(75) Racemates can be formed through the isomerization of chiral compounds.

(76) The chemist is racemizing the chiral molecule to study its properties.

(77) Acetals can be used as chiral building blocks in asymmetric synthesis.

(78) Cyanohydrin can be used as a chiral auxiliary in asymmetric synthesis.

(79) The observed dextrorotation suggested the presence of a chiral center.

(80) Racemized compounds can be detected using chiral analytical techniques.

Sentence using chiral

(81) Nitrones can be employed as chiral auxiliaries in asymmetric synthesis.

(82) The enantiomorphous crystals were used in chiral separation techniques.

(83) Hemiacetals can be used as chiral building blocks in organic synthesis.

(84) Benzylidines can be used as chiral auxiliaries in asymmetric synthesis.

(85) Pyrrolidine is also used as a chiral auxiliary in asymmetric synthesis.

(86) The synthesis of enantiomers often involves the use of chiral catalysts.

(87) Chiral molecules can exhibit different reactivity in chemical reactions.

(88) The racemization of chiral compounds can be catalyzed by acids or bases.

(89) Carbinols can be used as chiral building blocks in asymmetric synthesis.

(90) Organometallics have been employed in the synthesis of chiral compounds.

Chiral example sentence

(91) Enantiomorphism is studied extensively in the field of chiral chemistry.

(92) Investigate the role of isomerisms in the formation of chiral compounds.

(93) Enamines can be used as chiral auxiliaries in stereoselective reactions.

(94) The enantiomeric excess of the product was determined using chiral HPLC.

(95) The levorotary substance is commonly used as a chiral reference compound.

(96) The levorotation of a chiral molecule is due to its asymmetric structure.

(97) Alicyclics can be used as chiral building blocks in asymmetric synthesis.

(98) The enantiomorphs of the drug were separated using chiral chromatography.

(99) The enantiomorph of the compound was synthesized using a chiral catalyst.

(100) The chemist used a chiral catalyst to selectively isomerize the compound.

Sentence with word chiral

(101) Quinic acid is sometimes used as a chiral auxiliary in organic synthesis.

(102) The enantiomeric separation was achieved using a chiral stationary phase.

(103) The aldols can be used as chiral building blocks in asymmetric synthesis.

(104) Cycloadditions can be used to create chiral centers in organic molecules.

(105) The diastereoisomeric compounds were synthesized using a chiral catalyst.

(106) The imide group is often used as a chiral auxiliary in organic synthesis.

(107) Understanding stereochemistry is important for designing chiral catalysts.

(108) The achiral compound can be easily separated from its chiral counterparts.

(109) The enantiomeric excess of this reaction was determined using chiral HPLC.

(110) The use of a chiral ligand in the reaction improved the stereoselectivity.

Sentence of chiral

(111) The enantiomeric excess of this compound was determined using chiral HPLC.

(112) The enantiomers of this chiral catalyst have different catalytic activity.

(113) The separation of enantiomers is crucial in the production of chiral drugs.

(114) Cyanohydrins can be used as chiral building blocks in asymmetric synthesis.

(115) Chiral compounds are commonly used as building blocks in organic synthesis.

(116) Racemates can be resolved into their enantiomers using chiral HPLC columns.

(117) Organocopper reagents can be employed in the synthesis of chiral compounds.

(118) The chromatographer employed chiral chromatography to separate enantiomers.

(119) Pyrrolidine is commonly used as a chiral auxiliary in asymmetric synthesis.

(120) Achiral molecules are often used as reference compounds in chiral analysis.

Chiral used in a sentence

(121) The use of a chiral reagent improved the stereoselectivity of the reaction.

(122) Achiral compounds are often used as reference standards in chiral analysis.

(123) Diastereomers can be formed when a molecule has two or more chiral centers.

(124) The stereoselectivity of the reaction was improved by using a chiral ligand.

(125) The resolution of racemates is often achieved through chiral chromatography.

(126) The stereochemistry of ketoximes can be controlled by using chiral reagents.

(127) The separation of enantiomers can be achieved through chiral chromatography.

(128) The enantiomorphous crystals were used in chiral chromatography separations.

(129) The stereochemistry of cycloadditions can be controlled by chiral catalysts.

(130) Stereoisomerism is a result of the presence of chiral centers in a molecule.

Chiral sentence in English

(131) The stereoselectivity of the reaction was enhanced by using a chiral reagent.

(132) The racemization of chiral compounds can be influenced by temperature and pH.

(133) Racemates can be resolved into their enantiomers using chiral derivatization.

(134) Achiral compounds are often used as control substances in chiral separations.

(135) The chemist used a chiral catalyst to selectively transaminate the substrate.

(136) Chelate compounds have been used as chiral catalysts in asymmetric synthesis.

(137) The cholesteric phase is influenced by the concentration of chiral molecules.

(138) Scientists rely on the polarimeter to study the behavior of chiral molecules.

(139) Isocratic conditions are not suitable for the separation of chiral compounds.

(140) The presence of a chiral center in a molecule can give rise to stereoisomers.

(141) The racemate of this compound is often used in chiral resolution experiments.

(142) The derivatized amino acid was used as a chiral reagent in organic synthesis.

(143) The racemate can be resolved into its enantiomers using chiral chromatography.

(144) Sulfoxide compounds can be used as chiral auxiliaries in asymmetric synthesis.

(145) The racemic mixture was resolved into its enantiomers using a chiral catalyst.

(146) Aldolizations can be used to create chiral building blocks for drug synthesis.

(147) The compound's dextrorotation was affected by the presence of a chiral ligand.

(148) Isomerizing the chemical compound led to the formation of a new chiral center.

(149) The stereochemistry of annulations can be controlled by using chiral reagents.

(150) The antimeric form of a molecule can be separated using chiral chromatography.

(151) The enantiomorphs of the amino acid can be separated by chiral chromatography.

(152) The configurationally stable compound was synthesized using a chiral catalyst.

(153) The stereoselectivity of the reaction was enhanced by using a chiral auxiliary.

(154) The substituents on the chiral center determine the compound's stereochemistry.

(155) Scientists are investigating the enantiomorph's potential as a chiral catalyst.

(156) Imines can be used as starting materials for the synthesis of chiral compounds.

(157) The enantiomorphs of the compound can be separated using chiral chromatography.

(158) The use of alkoxides as catalysts can lead to the formation of chiral products.

(159) The chiral center was identified configurationally using X-ray crystallography.

(160) Levorotation is a result of the interaction between light and chiral molecules.

(161) Meso compounds are molecules that have a chiral center and a plane of symmetry.

(162) The enantiomeric separation of the racemic mixture was achieved by chiral HPLC.

(163) The stereochemistry of cyanohydrins can be controlled by using chiral catalysts.

(164) The racemization of chiral compounds can be reversible under certain conditions.

(165) Racemates can be resolved into their enantiomers using chiral stationary phases.

(166) The cyanoethylate group can be used to introduce a chiral group into a molecule.

(167) The dextrorotary sugar was used as a chiral building block in organic synthesis.

(168) The protonation of a molecule can result in the formation of a new chiral center.

(169) Stereospecific reactions can be influenced by the presence of chiral auxiliaries.

(170) Racemized amino acids can be used as chiral building blocks in organic synthesis.

(171) The stereospecific synthesis of the compound involved the use of chiral reagents.

(172) The achiral nature of the molecule made it less reactive towards chiral reagents.

(173) Glyceraldehyde is a chiral molecule, meaning it exists in two mirror-image forms.

(174) Isatin has been used as a starting material for the synthesis of chiral compounds.

(175) Biocatalysts can be used to produce chiral compounds with high enantioselectivity.

(176) The stereochemistry of cycloadditions can be controlled by using chiral catalysts.

(177) The stereochemistry of acetifications can be controlled by using chiral catalysts.

(178) Enamines can be used as catalysts in the asymmetric synthesis of chiral compounds.

(179) The presence of a chiral auxiliary enhanced the stereoselectivity of the reaction.

(180) Enantiomorphism is a phenomenon that arises due to the presence of chiral centers.

(181) Meso compounds are molecules that contain a chiral center and a plane of symmetry.

(182) The enantiomeric excess of the product was determined using chiral chromatography.

(183) The selectivity of epoxidation reactions can be enhanced by using chiral catalysts.

(184) The diastereomers can be resolved using chiral stationary phases in chromatography.

(185) The molecularity of a reaction can be affected by the presence of chiral molecules.

(186) The compound's dextrorotation was influenced by the presence of a chiral auxiliary.

(187) The study of enantiomorphs helps in understanding the behavior of chiral compounds.

(188) The chiral ligand played a crucial role in achieving the desired stereoselectivity.

(189) The stereospecific synthesis of the compound involved the use of a chiral catalyst.

(190) Enantiomorphism is an important consideration in the synthesis of chiral catalysts.

(191) The enantiomorphs of the chiral compound can exhibit different levels of chirality.

(192) The use of chiral catalysts can help to prevent racemization in chemical reactions.

(193) The metabolites were separated chromatographically using a chiral stationary phase.

(194) The understanding of enantiomorphism is essential in the design of chiral catalysts.

(195) Stereospecificity is important in the synthesis of chiral drugs and pharmaceuticals.

(196) The levorotation of a molecule can be influenced by the presence of a chiral center.

(197) The enantiomeric pair of this compound can be separated using chiral chromatography.

(198) The enantiomeric forms of this compound can be resolved using chiral derivatization.

(199) The cholesteric phase can be induced by adding chiral molecules to a liquid crystal.

(200) The use of a chiral catalyst greatly enhanced the stereoselectivity of the reaction.

(201) Enantiomorphism is a property that distinguishes chiral molecules from achiral ones.

(202) The stereospecific synthesis of the compound involved the use of a chiral auxiliary.

(203) Dextro is a term used in chemistry to describe the orientation of a chiral molecule.

(204) The study of racemates is crucial in understanding the behavior of chiral molecules.

(205) The racemized mixture of stereoisomers was resolved using a chiral stationary phase.

(206) The configuration of the stereocenter was determined configurationally by chiral GC.

(207) The racemized chiral center made it difficult to determine the molecule's structure.

(208) The unique stereochemistry of diolacton allows for the formation of chiral compounds.

(209) Levorotatory compounds are often used as chiral building blocks in organic synthesis.

(210) The racemic mixture was resolved into its enantiomers using a chiral resolving agent.

(211) The chiral catalyst played a crucial role in achieving the desired stereoselectivity.

(212) The enantiomorphs of the chiral catalyst can selectively catalyze specific reactions.

(213) The cyanohydrin synthesis is a useful method for the preparation of chiral compounds.

(214) The synthesis of stereoisomers often requires the use of chiral reagents or catalysts.

(215) The study of racemates is important in understanding the behavior of chiral molecules.

(216) The enantiomeric forms of this compound can be interconverted using a chiral catalyst.

(217) The reaction conditions must be carefully controlled when racemizing chiral molecules.

(218) Achiral molecules can be easily distinguished from chiral molecules using polarimetry.

(219) The stereoselectivity of the reaction was affected by the presence of a chiral solvent.

(220) The stereochemistry of epoxide opening reactions can be controlled by chiral catalysts.

(221) Achiral compounds can be resolved into their enantiomers using chiral resolving agents.

(222) Benzylidines have been used as starting materials in the synthesis of chiral compounds.

(223) The molecule can exist as diastereomers due to the presence of multiple chiral centers.

(224) The racemic acid was used as a starting material in the synthesis of a chiral compound.

(225) The separation of enantiomers is a critical step in the production of chiral pesticides.

(226) Nucleophilic attack on a carbon atom can result in the formation of a new chiral center.

(227) Enantiomorphism is a property that is often exploited in the production of chiral drugs.

(228) Stereoselective reactions often rely on the presence of chiral catalysts or auxiliaries.

(229) The enantiomeric excess of this reaction was determined using chiral gas chromatography.

(230) The epoxidation of chiral alkenes can be used to produce enantiomerically pure epoxides.

(231) The equimolecular mixture of the two enantiomers was separated by chiral chromatography.

(232) The enantiomeric excess of the reaction product was improved by using a chiral catalyst.

(233) The epoxidation of chiral alkenes can be used to create enantiomerically pure compounds.

(234) The presence of a chiral center in the molecule resulted in its dextrorotatory behavior.

(235) Stereospecific reactions can be used to create chiral catalysts for asymmetric synthesis.

(236) Enantiomeric resolution can be achieved using chiral stationary phases in chromatography.

(237) The stereochemistry of imines can be controlled by using chiral amine starting materials.

(238) The team used a chiral catalyst to acylate the substrate and obtain enantiopure products.

(239) Polarimeters are commonly used in the pharmaceutical industry to analyze chiral compounds.

(240) The racemization of chiral compounds can have significant implications in drug development.

(241) The unimolecular reaction was found to be influenced by the presence of a chiral auxiliary.

(242) The presence of a chiral center in a molecule can result in the formation of stereoisomers.

(243) Cyclodextrins have been used as chiral selectors in chromatography to separate enantiomers.

(244) The stereochemical stability of the chiral compound was studied under different conditions.

(245) The phenomenon of stereoisomerism arises due to the presence of chiral centers in molecules.

(246) Levorotatory substances can exhibit optical activity even in the absence of a chiral center.

(247) The racemic acid was converted into its pure enantiomer using a chiral resolution technique.

(248) The chiral ligand played a crucial role in achieving high stereoselectivity in the reaction.

(249) The stereoselective synthesis of the chiral compound required the use of a chiral auxiliary.

(250) The enantiomorphs of the chiral ligand can influence the stereochemistry of metal complexes.

(251) The synthesis of chiral thioureas has enabled the development of enantioselective reactions.

(252) Meso-tartaric acid is a compound that is commonly used in the synthesis of chiral molecules.

(253) The enantiomeric forms of the molecule have different interactions with chiral environments.

(254) Cyanohydrins can be used as chiral building blocks in the synthesis of enantiopure compounds.

(255) The use of chlorobromides in organic synthesis can lead to the formation of chiral compounds.

(256) The racemic mixture was resolved into its enantiomers using a chiral stationary phase in HPLC.

(257) Enantiomorphism is a property that arises due to the presence of a chiral center in a molecule.

(258) The dextrorotary configuration of the chiral center was determined using X-ray crystallography.

(259) The dextrorotary enantiomer was separated from the racemic mixture using chiral chromatography.

(260) The dextrorotatory property is determined by the configuration of chiral centers in a molecule.

(261) Stereoisomerism is often encountered in complex organic molecules with multiple chiral centers.

(262) The understanding of enantiomorphism is crucial in the synthesis of chiral drugs and catalysts.

(263) Refluxing the solution with a chiral auxiliary improved the enantioselectivity of the reaction.

(264) Meso-tartaric acid is a chiral molecule that is commonly used in organic chemistry experiments.

(265) The chiral auxiliary was used configurationally to control the stereochemistry of the reaction.

(266) The use of diolacton in asymmetric synthesis has led to the development of new chiral catalysts.

(267) The stereochemistry of epoxidation reactions can be controlled by the choice of chiral catalyst.

(268) The laevorotatory enantiomer was separated from the dextrorotatory enantiomer using chiral HPLC.

(269) The stereochemistry of amination reactions can be influenced by the presence of chiral catalysts.

(270) The levorotary compound can be separated from its dextrorotary isomer using chiral chromatography.

(271) Dextrorotatory compounds can be separated from levorotatory compounds using chiral chromatography.

(272) Achiral molecules can exhibit different physical properties compared to their chiral counterparts.

(273) Enantiomorphism is a property that distinguishes chiral molecules from their achiral counterparts.

(274) The reactivity of carbanions can be controlled through the use of chiral auxiliaries or catalysts.

(275) As the biocatalyst interacted with the substrate, it facilitated the formation of a chiral product.

(276) The levorotatory property of a compound can be influenced by the presence of other chiral molecules.

(277) The compound isomerized in the presence of a chiral catalyst, and the reaction produced enantiomers.

(278) The presence of laevorotatory amino acids in the protein was determined using chiral chromatography.

(279) The study of enantiomorphism has led to the development of techniques for separating chiral compounds.

(280) The dextrorotary configuration of the chiral center was crucial for the compound's biological function.

(281) The stereochemistry of an enamine can be controlled by the choice of chiral amine or carbonyl compound.

(282) If enantiomorphism is present, the molecules will have different interactions with chiral environments.

(283) The presence of multiple chiral centers in a molecule can give rise to a large number of stereoisomers.

(284) Levorotary compounds can be separated from their dextrorotary counterparts using chiral chromatography.

(285) The use of organozinc reagents in asymmetric synthesis has led to the development of new chiral ligands.

(286) The alicyclic structure of bicyclo[2.2.2]octane makes it a useful chiral auxiliary in organic synthesis.

(287) Achiral molecules can be easily distinguished from chiral molecules using certain analytical techniques.

(288) Racemization is a common problem in the synthesis of chiral drugs, as it can reduce their effectiveness.

(289) The study of enantiomorphism is crucial in understanding the properties and behavior of chiral compounds.

(290) The enantiomorphs were used as chiral catalysts, and their efficiency in promoting reactions was compared.

(291) The chemist observed dextrorotation in the reaction mixture, suggesting the formation of a chiral product.

(292) The study of enantiomorphism is important in understanding the properties and behavior of chiral compounds.

(293) The meso compound in chemistry refers to a molecule with a chiral center and an internal plane of symmetry.

(294) The use of chiral ligands in stereoselective reactions can greatly enhance the selectivity of the reaction.

(295) The professor emphasized the importance of enantiomorphs in understanding the behavior of chiral molecules.

(296) Levorotatory compounds can be separated from their dextrorotatory counterparts using chiral chromatography.

(297) The phenomenon of enantiomorphism can be observed in the behavior of light passing through chiral materials.

(298) The stereoselective synthesis of natural products often involves the use of chiral catalysts or auxiliaries.

(299) The use of chiral stationary phases in chromatographic separations allows for the separation of enantiomers.

(300) The two compounds are diastereomers because they have different configurations at one or more chiral centers.

(301) Hydroxylation can also be used to create chiral centers in molecules, which is important in drug development.

(302) The use of organolithium reagents in asymmetric synthesis has led to the development of new chiral compounds.

(303) The concept of enantiomorphism becomes more apparent when studying the optical properties of chiral molecules.

(304) Enantiomorphism is closely related to chirality, as it describes the relationship between two chiral molecules.

(305) The use of organocopper reagents in asymmetric synthesis has led to the development of many new chiral ligands.

(306) The enantiomorphs were separated using chiral chromatography, and their individual properties were investigated.

(307) The use of biocatalysis in the synthesis of chiral compounds can lead to more efficient and selective reactions.

(308) The enantiomorphs of the chiral catalyst can selectively catalyze the formation of one enantiomer over the other.

(309) Isomerisms can be used to study the properties of chiral compounds and their interactions with biological systems.

(310) If you introduce a chiral molecule to a biological system, it can interact differently with different enantiomers.

(311) The development of stereoselective methodologies has allowed for the efficient synthesis of chiral building blocks.

(312) The study of enantiomorphism is essential for understanding the behavior of chiral compounds in biological systems.

(313) The use of organocopper reagents in asymmetric synthesis has led to the development of many important chiral ligands.

(314) The stereospecificity of the reaction is crucial for the synthesis of chiral compounds with high enantiomeric purity.

(315) Racemization is a chemical process that converts a chiral molecule into a mixture of equal amounts of its enantiomers.

(316) The study of enantiomorphism allows scientists to understand the different properties and behaviors of chiral molecules.

(317) The application of biocatalysts in the synthesis of chiral compounds is of great interest to the pharmaceutical industry.

(318) Racemization is a common problem in the synthesis of chiral drugs, as it can lead to decreased efficacy or even toxicity.

(319) The polarimeter measured a significant degree of dextrorotation in the sample, indicating the presence of a chiral center.

(320) The enantiomorphs of the compound can be separated using chiral chromatography, or they can be resolved by crystallization.

(321) Isomerisms, such as optical isomerism, occur when molecules have a chiral center, resulting in the existence of enantiomers.

(322) The stereochemistry of a reaction can be influenced by the presence of chiral auxiliaries in a stereoselective transformation.

(323) The enantiomorphs of the molecule have identical chemical properties, but they differ in their interactions with chiral environments.

(324) The two compounds are enantiotopic, which means they are stereoisomers that can be distinguished by their behavior in a chiral environment.

(325) Isomerizations, which can be influenced by the presence of chiral centers, are important in the production of enantiomerically pure compounds.

(326) The chiral auxiliary used in the synthesis resulted in a product with dextrorotation, indicating the desired stereochemistry had been achieved.

(327) The enantiomorphs of the molecule can be synthesized using chiral catalysts, and their stereochemistry can be confirmed by X-ray crystallography.

(328) The enantiomorphs of the compound can be separated using chiral stationary phases in chromatography, or they can be resolved by kinetic resolution.

(329) The enantiomorphs of the compound can be separated using chiral additives in chromatography, or they can be resolved by enzymatic kinetic resolution.

(330) The study of enantiomorphism has led to the development of new methods for the synthesis of chiral compounds, which are essential building blocks in drug discovery.

The word usage examples above have been gathered from various sources to reflect current and historical usage of the word Chiral. They do not represent the opinions of TranslateEN.com.