metal-free stereoselective catalytic addition of in situ generated dienamine to b-nitroacrylates has been developed. Starting from simple a,bunsaturated ketones, highly functionalized chiral bnitrocyclohexanecarboxylic esters were obtained in a single step, in good yields and up to 98% ee. By an unprecedented mechanistic pathway, starting from the synthetically readily available E-nitroacrylate, the present methodology allowed us to obtain as major product the isomer bearing a cis relative disposition between the nitro and the ester groups, which is not accessible via a classical Diels–Alder reaction.

Stereoselective Synthesis of Functionalized Chiral 2-Nitrocyclohexanecarboxylic Esters via Catalytic Dienamine Addition to b-Substituted b-Nitroacrylates

PALMIERI, Alessandro;
2014-01-01

Abstract

metal-free stereoselective catalytic addition of in situ generated dienamine to b-nitroacrylates has been developed. Starting from simple a,bunsaturated ketones, highly functionalized chiral bnitrocyclohexanecarboxylic esters were obtained in a single step, in good yields and up to 98% ee. By an unprecedented mechanistic pathway, starting from the synthetically readily available E-nitroacrylate, the present methodology allowed us to obtain as major product the isomer bearing a cis relative disposition between the nitro and the ester groups, which is not accessible via a classical Diels–Alder reaction.
2014
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11581/313585
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