AI Article Synopsis

Article Abstract

Viedma ripening is a process that combines abrasive grinding of a slurry of crystals with solution-phase racemization, resulting in solid-phase deracemization. One of the major disadvantages of Viedma ripening is that the desired compound needs to crystallize as a racemic conglomerate, accounting for only 5-10 % of all chiral molecules. Herein, we show that use of a chiral additive causes deracemization under conditions, in which the compound normally crystallizes as a racemic compound. Although this concerns a single example, it is envisioned that through this new approach the scope of Viedma ripening can be significantly expanded.

Download full-text PDF

Source
http://dx.doi.org/10.1002/chem.201706088DOI Listing

Publication Analysis

Top Keywords

viedma ripening
12
racemic compound
8
deracemization racemic
4
compound
4
compound tailor-made
4
tailor-made additives
4
additives viedma
4
ripening process
4
process combines
4
combines abrasive
4

Similar Publications

Attrition-enhanced chiral symmetry breaking in crystals, known as Viedma deracemization, is a promising method for converting racemic solid phases into enantiomerically pure ones under non-equilibrium conditions. However, many aspects of this process remain unclear. In this study, we present a new investigation into Viedma deracemization using a comprehensive kinetic rate equation continuous model based on classical primary nucleation theory, crystal growth, and Ostwald ripening.

View Article and Find Full Text PDF
Article Synopsis
  • Aldehydes and carboxylic acids are effective catalysts for racemizing amino acids, but the exact mechanisms are not fully understood.
  • The study focuses on aspartic acid racemization, utilizing salicylaldehyde and acetic acid, employing computational methods to analyze the reaction pathways.
  • Findings reveal that the dehydration step presents the highest energy barrier in the process, while the presence of water significantly lowers the energy required for this step, facilitating racemization.
View Article and Find Full Text PDF

A Greener Pathway to Enantiopurity: Mechanochemical Deracemization through Abrasive Grinding.

Chemistry

June 2023

Department of Molecular Chemistry, Materials and Catalysis, Institute of Condensed Matter and Nanosciences, Université Catholique de Louvain, Place Louis Pasteur, 1 bte L4.01.06, 1348, Louvain-La-Neuve, Belgium.

We report the first case of mechanochemical deracemization by using liquid-assisted abrasive grinding. The target molecule is a precursor of Paclobutrazol, an important fungicide and plant growth inhibitor. Using mechanochemical deracemization, we are even able to transform a 10 % ee scalemic mixture of this latter in an enantioenriched product of 97 % ee in a couple of hours.

View Article and Find Full Text PDF

Chiral crystals remain one of the probable sources of first minute chiral symmetry breaking, a trigger that potentially causes an as-yet unknown type of asymmetric autocatalysis during the formation of chiral biopolymers under the conditions of the Archean Earth. Therefore, studying adsorption processes on the surface of such crystals may help improve the understanding of the nature of the initial chiral shift. The adsorptive activity of non-porous crystals with respect to the majority of organic molecules essentially depends on the ability of a crystal surface to engage in specific intermolecular interactions.

View Article and Find Full Text PDF

Enantiomeric purity is of prime importance for several industries, specifically in the production of pharmaceuticals. Crystallization processes can be used to obtain pure enantiomers in a suitable solid form. However, some process variants inherently rely on kinetic enhancement (preferential crystallization) of the desired enantiomer or on complex interactions of several phenomena (e.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!