Line-shape analysis of 31P NMR spectra of catalyst substrate complexes of seven-membered ring rhodium(I)-bisphosphinites indicate for the first time a quantifiable preference of the intramolecular major–minor isomerisation of both diastereoisomeric chelates of dimethyl itaconate over the slow intermolecular interconversion.
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Kadyrov et al. (1995) studied this question.
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