1,3 dipolar cycloaddition of münchnones: Factors behind the regio-selectivity

07 September 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The 1,3 dipolar cycloaddition reactions of münchnones and alkenes provide an expedite synthetic way to substituted pyrroles, an exceedingly important structural motif in the pharmaceutical and material science fields of research. The factors governing their regio-selectivity rationalization are not well understood. Using several approaches, we investigate a set of 14 reactions (featuring two münchnones, 12 different alkenes, and two alkynes). The Natural Bond Theory and the Non-Covalent Interaction Index analyses of the non-covalent interaction energies fail to predict the experimental major regio-isomer. Employing global cDFT descriptors or local ones such as the Fukui function and dual descriptor yields similarly inaccurate predictions. Only the local softness pairing, withing Pearson's Hard and Soft Acids and Bases principle, constitutes a reliable predictor for the major reaction product. By taking into account an estimator for the steric effects, the correct regio-isomer is predicted. Steric effects play a major role in driving the regio-selectivity, as was corroborated by energy decomposition analysis of the transition states.

Keywords

dipolar cycloadditions
münchnones
NBO
NCI
conceptual DFT

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