Reactivity of Woollins' Reagent toward 2-En-1-imines (Schiff Bases): A Facile Approach to Synthesize New Selenium-Phosphorus-Nitrogen Heterocycles
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DOI: 10.1002/ejic.201901030
Abstract: Woollins’ Reagent serves as a reductive cycloaddition reagent, reacting with 2-en-1-imines containing a conjugated C=C bond group (Schiff bases) leading to a series of four-, five-, sixmembered 1,2-azaphospholidines incorporating one or two N-P=Se linkages. Ten… read more here.
Keywords: schiff bases; woollins reagent; imines schiff; toward imines ... See more keywords
Woollins’ reagent promotes selective reduction of α,β-unsaturated thiazo and selenazolidinones
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DOI: 10.1016/j.tetlet.2017.02.053
Abstract: Abstract In this work we describe the Woollins’ reagent as useful for the selective reduction of the double bond of 2-α,β-unsaturated thiazo and selenazolidinones. The reaction took place in toluene at room temperature to give… read more here.
Keywords: selective reduction; woollins reagent; thiazo selenazolidinones; reagent promotes ... See more keywords