Selective Functionalization of Achmatowicz Rearrangement Products by Reactions with Potassium Organotrifluoroborates under Transition-Metal-Free Conditions
journal contributionposted on 23.07.2018, 00:00 by Silvia Roscales, Víctor Ortega, Aurelio G. Csákÿ
The repertoire of synthetic transformations of the products of the Achmatowicz rearrangement has been expanded by exploring their reactivity with potassium organotrifluoroborates in the absence of transition metals. Depending on the reaction conditions and the substitution pattern of the starting material, the reaction may lead to the stereoselective synthesis of dihydropyranones (2,6-trans), tetrahydropyranones (2,3-cis-2,6-cis) or functionalized 1,4-dicarbonyl compounds. The method has also been adapted for the one-pot synthesis of functionalized pyrroles.
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reaction conditionscompoundcifunctionalized pyrrolesstereoselective synthesistransition metalsone-pot synthesispotassium organotrifluoroboratesabsencedihydropyranonedicarbonylreactivitytransformationAchmatowicz rearrangementAchmatowicz Rearrangement ProductsTransition-Metal-Free ConditionsmaterialPotassium OrganotrifluoroboratesrepertoireSelective Functionalizationmethodtetrahydropyranonesubstitution pattern