Accelerating Spirocyclic Polyketide Synthesis
News Oct 30, 2014
The modular Asia flow chemistry system from Syrris proved key to the success of a recently described process for accelerated total synthesis of spirodienal A and spirangien A methyl ester.
Developed by the Ley Group at the Department of Chemistry, University of Cambridge, UK - and recently published in Angewandte Chemie International Edition - the work describes the use of powerful flow chemistry techniques for complex multi-stage synthesis of spirocyclic polyketides.
The flexible Asia system was crucial to the success of the study, offering a variety of flow techniques - including gas-liquid and solid phase chemistries, liquid-liquid extraction and continuous work-up - to enable faster reaction optimization and telescoping of reaction steps.
Researchers benefitted from the Asia Pump’s capacity to smoothly handle low boiling point solvents, as well as rapid mixing and continuous work-up in glass microreactors with the advanced Asia FLLEX (Flow Liquid Liquid Extraction).
This set-up allowed synthesis of essential, complex coupling fragments using newly developed flow chemistry methods for automated reagent addition, silylation, crotylation, ozonolysis, olefination and oxidation, allowing these vital building blocks to be produced faster and more safely, with higher yields compared to batch reactions.
Researchers have developed an artificial enzymatic pathway for synthesizing isoprenoids, or terpenes, in E. coli. This shorter, more efficient, cost-effective and customizable pathway transforms E. coli into a factory that can produce terpenes for use in everything from cancer drugs to biofuels.READ MORE