Abstract

In the past decade mechanochemical methodologies, such as neat grinding and liquid-assisted grinding, have been demonstrated to be a highly efficient means of both synthesising and screening for pharmaceutical co-crystals. This chapter provides an overview of these mechanochemical methodologies, their applications to date, an overview of mechanistic details and a brief comparison with more conventional co-crystallisation methods based on solution crystallisation and slurrying. In addition to the use of mechanosynthesis in the context of pharmaceutical co-crystals, its application for pharmaceutical salt synthesis and screening is also described, as well as recent applications in the synthesis of metal–organic derivatives.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.