Abstract
Herein reported is a strategy for constructing vicinal 4°/3° carbons via reductive Cope rearrangement. Substrates have been designed which exhibit Cope rearrangement kinetic barriers in the range of ~23 kcal/mol with isothermic favorability (G ~0). These fluxional/shape-shifting molecules can be driven forward by chemoselective reduction to useful polyfunctionalized building blocks.
Supplementary materials
Title
Supporting Information
Description
Experimental procedures
Spectroscopic Data (1H HMR, 13C NMR , HRMS) and spectral reprints (1H NMR and 13C NMR)
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