Origins of stereoselectivity in Diels-Alder cycloadditions catalyzed by chiral imidazolidinones

Engineering & Materials Science

• Stereoselectivity 100%
• Cycloaddition 96%
• Enantioselectivity 96%
• Reaction intermediates 84%
• Density functional theory 71%
• Aldehydes 69%
• Ketones 68%
• Conformations 60%

Medicine & Life Sciences

• Cyclopentanes 83%
• Density Functional Theory 83%
• Cycloaddition Reaction 80%
• Ketones 60%
• Aldehydes 57%

Chemical Compounds

• Imidazolidinone 71%
• Diels-Alder Cycloaddition 61%
• Stereoselectivity 44%
• Cyclopentadiene 27%
• Reaction Intermediate 25%
• Diels-Alder Reaction 22%
• Enantioselectivity 20%
• Aldehyde 16%
• Density Functional Theory 14%