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1.
SLAS Technol ; 29(3): 100135, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38703999

ABSTRACT

Laboratory management automation is essential for achieving interoperability in the domain of experimental research and accelerating scientific discovery. The integration of resources and the sharing of knowledge across organisations enable scientific discoveries to be accelerated by increasing the productivity of laboratories, optimising funding efficiency, and addressing emerging global challenges. This paper presents a novel framework for digitalising and automating the administration of research laboratories through The World Avatar, an all-encompassing dynamic knowledge graph. This Digital Laboratory Framework serves as a flexible tool, enabling users to efficiently leverage data from diverse systems and formats without being confined to a specific software or protocol. Establishing dedicated ontologies and agents and combining them with technologies such as QR codes, RFID tags, and mobile apps, enabled us to develop modular applications that tackle some key challenges related to lab management. Here, we showcase an automated tracking and intervention system for explosive chemicals as well as an easy-to-use mobile application for asset management and information retrieval. Implementing these, we have achieved semantic linking of BIM and BMS data with laboratory inventory and chemical knowledge. Our approach can capture the crucial data points and reduce inventory processing time. All data provenance is recorded following the FAIR principles, ensuring its accessibility and interoperability.


Subject(s)
Automation, Laboratory , Automation, Laboratory/methods , Laboratories , Information Storage and Retrieval/methods
2.
Angew Chem Int Ed Engl ; 53(22): 5643-7, 2014 May 26.
Article in English | MEDLINE | ID: mdl-24737675

ABSTRACT

An enantioselective synthesis of spiropyrazolones from allenoate-derived MBH acetates and pyrazolones through a phosphine-mediated [4+1] annulation process has been developed. Spiropyrazolones were readily prepared in good chemical yields and good to high enantioselectivities. This is the first asymmetric example in which α-substituted allenoates were utilized as a C4 synthon for phosphine-catalyzed [4+1] annulation.


Subject(s)
Phosphines/chemistry , Pyrazolones/chemistry , Spiro Compounds/chemistry , Catalysis , Crystallography, X-Ray , Cycloaddition Reaction , Molecular Conformation , Pyrazolones/chemical synthesis , Stereoisomerism
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