Topic
Oxazolidine
About: Oxazolidine is a research topic. Over the lifetime, 1516 publications have been published within this topic receiving 13602 citations.
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TL;DR: Both regioisomers of enantioenriched 1,2-aminoalcohols can be obtained using oxaziridine-mediated oxyamination reactions, and the overall sense of regiochemistry can be controlled using the appropriate choice of inexpensive first-row transition metal catalyst.
Abstract: The regioselective and enantioselective oxyamination of alkenes with N-sulfonyl oxaziridines is catalyzed by a novel iron(II) bis(oxazoline) complex. This process affords oxazolidine products that can be easily manipulated to yield highly enantioenriched free amino alcohols. The regioselectivity of this process is complementary to that obtained from the analogous copper(II)-catalyzed reaction. Thus, both regioisomers of enantioenriched 1,2-aminoalcohols can be obtained using oxaziridine-mediated oxyamination reactions, and the overall sense of regiochemistry can be controlled using the appropriate choice of inexpensive first-row transition metal catalyst.
141 citations
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TL;DR: The incorporation of serine as oxazolidine protected “pseudo proline “in a host peptide results in the disruption of secondary structure formation thus increasing the solvation of the peptide chain.
133 citations
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TL;DR: In this paper, the stereoselectivity of imines of benzaldehyde and cinnamaldehyde with ketenes generated by the reaction of optically active oxazolidinone acid chlorides with triethylamine was compared.
Abstract: The stereoselectivity of the reaction of imines of benzaldehyde and cinnamaldehyde with ketenes generated by the reaction of optically active oxazolidinone acid chlorides with triethylamine and complexed ketenes generated by photolysis of optically active oxazolidine ― and oxazolidinone-chromium-carbene complexes in the presence and absence of added triethylamine was compared. The absolute stereochemistry was determined primarily by the structure of the chiral auxiliary. The relative (cis-trans) stereochemistry was determined primarily by the structure of the imine and the free or bound character of the ketene. Triethylamine addition to reactions of carbene complexes afforded results that closely paralleled that of acid chloride generated ketenes. A mechanistic scheme accounting for these results and the general trends observed in other ketene/imine cyclizations is provided
129 citations
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TL;DR: 2-tert-Butyldiphenylsilylmethyl-substituted aziridine and the corresponding azetidine reacted efficiently with nitriles and carbonyl substrates to generate imidazoline, oxazolidine, and tetrahydropyrimidine products.
Abstract: 2-tert-Butyldiphenylsilylmethyl-substituted aziridine and the corresponding azetidine reacted efficiently with nitriles and carbonyl substrates to generate imidazoline, oxazolidine, and tetrahydropyrimidine products. The azetidine rearranged efficiently to the pyrrolidine skeleton involving migration of silicon under BF3·Et2O conditions. The tert-butyldiphenylsilylmethyl function, latent to CH2OH group, controlled not only the regioselectivity of aziridine and azetidine cleavage but also the relative stereochemistry of the substituents in the products derived from substituted aziridine.
116 citations
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TL;DR: An efficient and stereoselective reaction between 3-isothiocyanato oxindoles and isatins/isatinimines has been developed to afford structurally diverse dispiro[oxazolidine-2-thione]bisoxindoles in excellent results under mild conditions.
108 citations