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J Org Chem
; 79(17): 8304-12, 2014 Sep 05.
Article
in English
| MEDLINE
| ID: mdl-25068678
ABSTRACT
Cycloadditions of 1,3-dipoles and related species to a cis-oxabicyclo[3.3.0]octenone occur on the more sterically crowded concave face. These cycloadditions were studied experimentally by Gais and co-workers in 1998 (Eur. J. Org. Chem. 1998, 257-273) and have now been studied computationally with density functional theory (DFT). Transition states have been computed for various types of (3 + 2) cycloadditions, including diazomethane 1,3-dipolar cycloadditions, a thermally promoted methylenecyclopropane acetal cycloaddition, and a Pd-catalyzed cycloaddition of methylenecyclopropane to an oxabicyclo[3.3.0]octenone. The concave stereoselectivities arise from alkene predistortion that leads to torsional steering in the transition states.