Brief introduction of (R)-4-Benzyl-2-oxazolidinone

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102029-44-7, Name is (R)-4-Benzyl-2-oxazolidinone, belongs to oxazolidine compound, is a common compound. Product Details of 102029-44-7In an article, once mentioned the new application about 102029-44-7.

Dirhodium(II) tetrakis(carboxamidates) with chiral ligands. Structure and selectivity in catalytic metal-carbene transformations

Structure-selectivity comparisons are made between chiral dirhodium(II) tetrakis(methyl 2-oxopyrrolidine5-carboxylates), Rh2(5S-MEPY)4 and Rh2(5R-MEPY)4 (5), and dirhodium(II) tetrakis(4-benzyl-2- oxazolidinones), Rh2(4R-BNOX)4 and Rh2(4S-BNOX)4 (6), to ascertain and understand their relative effectiveness as catalysts for enantiocontrol in metal-carbene transformations. The syntheses, spectral characteristics, and X-ray structures for these dirhodium(II) compounds are reported. Each possesses two oxygen- and two nitrogen-donor atoms bound to each . octahedral rhodium with a cis orientation of the nitrogen ligands. The Rh2(MEPY)4 catalysts are significantly more effective than those of Rh2(BNOX)4 in providing a high level of enantiocontrol in intermolecular and intramolecular cyclopropanation reactions, in intermolecular cyclopropenation reactions, and in intramolecular C-H insertion reactions of diazoacetates and diazoacetamides, often reaching >90% enantiomeric excesses. Molecular mechanics calculations that were able to reproduce the X-ray structures of Rh2(5S-MEPY)4 and Rh2(4R-BNOX)4 have been employed to obtain the preferred conformation of the intermediate metal-carbene, but the absolute configurations of cyclopropanation products are opposite to those predicted from the preferred metal-carbene conformation. However, conformational energy minima of the styrene-carbene complex predict the observed enantiomer preference.

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Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H1803NO – PubChem