3 article(s) from Jawiczuk, Magdalena
Asymmetric α-photooxygenation of chiral aldehydes.
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α-Photooxygenation of β-substituted aldehydes.
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Synthesis and α-photooxygenation of 3,4-diphenylbutanal (1).
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Stereoselective α-photooxygenation of 3,4-diphenylbutanal (1) with 1O2.
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Schematic representation of the in situ methodology and preferred conformation of diols with Mo2 co...
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ECD spectra of diols syn-6 and anti’-6 recorded a) with 19 in DMSO and b) in acetonitrile compared ...
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Asymmetric synthesis of 3,4-diphenylbutane-1,2-diol.
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Beilstein J. Org. Chem. 2019, 15, 2076–2084, doi:10.3762/bjoc.15.205
NHC’s and their ruthenium complexes studied in this work; L = carbene 1, 2 or 3.
Schematic representation of carbene dimerization and atom numbering scheme used throughout this wor...
Dissociative mechanism of initiation for Grubbs-like 1–3-GrI and M1 indenylidene type complexes 1–3...
Dissociative mechanism of initiation of 2nd generation Grubbs-like saturated 1–3-GrII and unsaturat...
Dissociative mechanism of activation for complexes 1–3-Hov; L = carbene 1, 2 or 3.
Beilstein J. Org. Chem. 2018, 14, 2872–2880, doi:10.3762/bjoc.14.266
Examples of sucrose-based macrocycles.
Synthesis of higher sugar precursors by a Wittig-type methodology.
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Synthesis of higher sugar enone 10.
Synthesis of the diol 13 containing two sucrose units.
CD spectra of in situ formed chiral complexes of 13 (green line), 14 (purple line) and 16 (blue lin...
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Synthesis of model sucrose diols.
Beilstein J. Org. Chem. 2014, 10, 1246–1254, doi:10.3762/bjoc.10.124
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