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Computational analysis evaluates NMR spectra and stereochemical assignments of cyclopropane products from enal cyclopropanation, suggesting precision in product characterization.
In the previous post, I investigated the mechanism of cyclopropanation of an enal using a benzylic chloride using a quantum chemistry based procedure. Here I take a look at the NMR spectra of the resulting cyclopropane products, with an evaluation of the original stereochemical assignments.
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Henry S. Rzepa (2018) studied this question.
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