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Regioselectivity of the Claisen Rearrangement in meta-Allyloxy Aryl Ketones: An Experimental and Computational Study, and Application in the Synthesis of (R)-(−)-Pestalotheol D

✍ Scribed by Catherine L. Lucas; Prof. Dr. Barry Lygo; Prof. Dr. Alexander J. Blake; Dr. William Lewis; Prof. Dr. Christopher J. Moody


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
305 KB
Volume
17
Category
Article
ISSN
0947-6539

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✦ Synopsis


Abstract

A study of the regioselectivity of the Claisen rearrangement of meta‐allyloxy aryl ketones showed that the electron‐withdrawing carbonyl group has a major influence and strongly directs rearrangement to the more hindered ortho position. However, when the ketone is part of a ring structure, its electronic effect can be negated by conversion into its triisopropylsilyl enol ether, which dramatically reverses the regiochemistry of the Claisen rearrangement. DFT calculations suggest that the effect is electronic although there is also a steric effect of the bulky silyl group. This strategy for influencing the regiochemical outcome of the Claisen rearrangement was then employed in a short synthesis of the furo[2,3‐g]chromene, (−)‐pestalotheol D, that confirms the absolute stereochemistry of the natural product.