https://www.selleckchem.com/products/OSI-906.html
A redox neutral CIII)-catalyzed annulation of α,β-unsaturated oxime ether with alkyne has been reported. Multisubstituted pyridines were synthesized in good yields without the use of any heavy metal oxidants. The developed methodology tolerates a variety of functional groups. Notably, this transformation has been applied to the late-stage modification of the bioactive molecule dehydropregnenolone.Reduced-scaling methods are needed to make accurate and systematically improvable coupled cluster linear response methods for the calculatio
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