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Volumn 47, Issue 35, 2008, Pages 6707-6711

Functional analysis of an aspartate-based epoxidation catalyst with amide-to-alkene peptidomimetic catalyst analogues

Author keywords

Asymmetric catalysis; Epoxidation; Fluorine; Olefin isostere; Peptides; Peptidomimetic

Indexed keywords

AMIDES; AMINES; CHEMICAL REACTIONS; INTEGRAL EQUATIONS; OLEFINS;

EID: 52449099149     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200802223     Document Type: Article
Times cited : (120)

References (59)
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    • The details of the synthesis and characterization data can be found in the Supporting Information
    • The details of the synthesis and characterization data can be found in the Supporting Information.
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    • A colorless block crystal (0.25 × 0.20 × 0.20 mm3) was mounted with epoxy cement on the tip of a fine glass fiber. All measurements were made on a Bruker Nonius Kappa CCD diffractometer with graphite monochromated MoKa radiation. The data were corrected for Lorentz and polarization effects. The data frames were processed and scaled using the DENZO software package. The structure was solved by direct methods and expanded using Fourier techniques. The non-hydrogen atoms were refined anisotropically and hydrogen atoms were treated as idealized contributions. C23H 33N3Ox5·CH2Cl2= C24H35Cl2N3O5 (8, Mr=516.45 gmol-1, orthorhombic, space group P212121, 19, a, 9.0028(18, b, 11.376(2, c, 26.325(5) Å, α, 90°, β
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    • The relative stereochemical relationships were shown by X-ray analysis of the amino alcohol derived from 21 (CCDC 687521). Details of the synthesis can be found in the Supporting Information.
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