Abstract
We describe a formal 1,3-dipolar cycloaddition between bicyclobutanes and pyridinium ylides to form azabicycloheptanes via diastereoselective pyridine dearomatization. Microscale highthroughput experimentation led to identification of conditions affording high yield and stereoselectivity without the need for catalysis. These reactions proceed using as-received reagents and solvents under ambient atmosphere. The resulting ring-fused azabicyclo[3.1.1]heptanes have diverse synthetic handles for further transformations, making them potentially valuable scaffolds for the design of Csp3-rich drug candidates. We also demonstrate a diastereoselective photochemical skeletal rearrangement to give a 1,1,3,3-tetrasubstitued cyclobutane.
Supplementary materials
Title
Supporting Information
Description
Detailed experimental procedures, screening data, characterization data/spectra, and X-ray crystallography details.
Actions
Title
3c CIF
Description
Crystallographic information file for solid state structure of compound 3c
Actions
Title
4b CIF
Description
Crystallographic information file for solid state structure of compound 4b
Actions