The determination of the absolute configuration of chiral molecular entities by means of X-ray crystallography is overall of central importance in stereochemistry. However, the growth of enantiopure single crystals often represents an unsurmountable and frustrating hurdle. Quasi-racemic crystals of biomacromolecules, for which the absolute configuration is predetermined by the chiral monomers, allowed the X-ray crystallographic analysis of systems that are difficult to crystallize as pure enantiomers, with aims other than the determination of the absolute structure. Taking advantage of the greater propensity of quasi-racemic mixtures to co-crystallize compared to growing enantiomerically pure crystals of a single compound, we herein describ...
When chiral compounds with low enantiomeric excess (ee, R:S=m:n) were absorbed into the void of the ...
Absolute stereochemistry of oils and viscous liquids can be difficult to determine. Co-crystallizat...
Cocrystallization of racemic-compound-forming chiral molecules can result in conglomerate cocrystals...
Objectives of this project are: (1) Understanding of the factors that control the formation of enan...
A large number of active pharmaceutical ingredients (API) are chiral. Most of them are synthesized a...
[EN] The X-ray crystal structure of a racemic triarylcarbinol derivate ((±)-1) was determined. Comp...
Two enantiomers of the same chiral active pharmaceutical ingredients (APIs) often have different pha...
Chiral molecules are asymmetrical objects, and from this geometric property emerge enantiomers, that...
none4sicrystal engineering, cocrystals, chiralityThe coordination mode to lithium, magnesium, calciu...
The study of cocrystals is a research topic that is recently on the rise, particularly in the pharma...
A large number of active pharmaceutical ingredients (API) are chiral. Most of them are synthesized a...
International audienceDue to the chirality of life, the two enantiomers of chiral molecules can exhi...
During the past decades, the rapid development in diffraction techniques has provided lot of informa...
Preferential crystallization, as a powerful chiral resolution technique, is intrinsically limited to...
A large number of active pharmaceutical ingredients (API) are chiral. Most of them are synthesized a...
When chiral compounds with low enantiomeric excess (ee, R:S=m:n) were absorbed into the void of the ...
Absolute stereochemistry of oils and viscous liquids can be difficult to determine. Co-crystallizat...
Cocrystallization of racemic-compound-forming chiral molecules can result in conglomerate cocrystals...
Objectives of this project are: (1) Understanding of the factors that control the formation of enan...
A large number of active pharmaceutical ingredients (API) are chiral. Most of them are synthesized a...
[EN] The X-ray crystal structure of a racemic triarylcarbinol derivate ((±)-1) was determined. Comp...
Two enantiomers of the same chiral active pharmaceutical ingredients (APIs) often have different pha...
Chiral molecules are asymmetrical objects, and from this geometric property emerge enantiomers, that...
none4sicrystal engineering, cocrystals, chiralityThe coordination mode to lithium, magnesium, calciu...
The study of cocrystals is a research topic that is recently on the rise, particularly in the pharma...
A large number of active pharmaceutical ingredients (API) are chiral. Most of them are synthesized a...
International audienceDue to the chirality of life, the two enantiomers of chiral molecules can exhi...
During the past decades, the rapid development in diffraction techniques has provided lot of informa...
Preferential crystallization, as a powerful chiral resolution technique, is intrinsically limited to...
A large number of active pharmaceutical ingredients (API) are chiral. Most of them are synthesized a...
When chiral compounds with low enantiomeric excess (ee, R:S=m:n) were absorbed into the void of the ...
Absolute stereochemistry of oils and viscous liquids can be difficult to determine. Co-crystallizat...
Cocrystallization of racemic-compound-forming chiral molecules can result in conglomerate cocrystals...