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Asymmetric hydrogenation of ( Z )-2-benzoylamino-3-(3,4-dimethoxyphenyl)-methyl acrylate with [Rh(( S, S )-DIPAMP)(MeOH) 2 ]BF 4 was investigated. Low temperature NMR measurements prove the recently published X-ray structure of [Rh(( S, S )-DIPAMP)(( Z )-2-benzoylamino-3-(3,4-dimethoxyphenyl)-methyl acrylate)]BF 4 to be the major substrate complex. The asymmetric hydrogenation of the prochiral DOPA precursor with the cationic Rh-DIPAMP catalyst therefore follows the “anti-lock-and-key” motif analogue to similar substrate complexes already known from literature.
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Schmidt et al. (2005) studied this question.
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