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. Author manuscript; available in PMC: 2015 Feb 1.
Published in final edited form as: Nat Commun. 2014 Aug 1;5:4455. doi: 10.1038/ncomms5455

Figure 3.

Figure 3

Stereoelectronic considerations for an oxy-Cope rearrangement. Cyclohexane A–values for carbomethoxy (a) and hydroxy (b) substituted cyclohexanes. Manifestation of stereoelectronic effects in the competition between two chair-like transition states (III and III´).