Not antiaromaticity gain, but increased asynchronicity enhances the Diels-Alder reactivity of tropone.

Chem Commun (Camb)

Department of Theoretical Chemistry, Amsterdam Institute of Molecfular and Life Sciences (AIMMS), Amsterdam Center for Multiscale Modeling (ACMM), Vrije Universiteit Amsterdam, De Boelelaan 1083, Amsterdam 1081 HV, The Netherlands.

Published: March 2023

Tropone is an unreactive diene in normal electron demand Diels-Alder reactions, but it can be activated carbonyl umpolung by using hydrazone ion analogs. Recently, the higher reactivity of hydrazone ion analogs was ascribed to a raised HOMO energy induced by antiaromaticity (L. J. Karas, A. T. Campbell, I. V. Alabugin and J. I. Wu, . ., 2020, , 7083). We show that this is incorrect, and that the activation barrier is lowered by increased asynchronicity.

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Source
http://dx.doi.org/10.1039/d3cc00512gDOI Listing

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