H. Jendralla scite author profile

Peptide aldehydes 15a-c are protocol for the preparation and utilizaprepared without epimerization from tion of THF solutions of 11, the isolation enantiomerically pure (S)-a-amino acids of air-sensitive intermediates can be (Scheme 3). Reductive pinacol homocoupling of 15a-c, induced by vanadium complex 11 or niobium complex 16 in refluxing THF, yields C,-symmetrical (S,R,R,S)-configurated 6a, 6 b and 2, respectively, with moderate to high stereoselectivity (Scheme 4). In a novel

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Efficient synthesis of (R)- and (S)-(6,6′-difluorobiphenyl-2,2′-diyl) bis(diphenylphosphine); electron-poor biphenyl-type ligands for transition metal catalysts.

Jendralla

Paulus

1994

Tetrahedron: Asymmetry

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Diastereo- and Enantioselective Synthesis of Ferrocenylphosphines by Twofold AsymmetricOrtho-Lithiation

Jendralla

Paulus

1997

Synlett

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Stereoselective synthesis of HR 780 a new highly potent HMG-CoA reductase inhibitor

Wess¹,

Keßeler²,

Baader³

et al. 1990

Tetrahedron Letters

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H. Jendralla

Practical Large Scale Synthesis of tert-Butyl (3R,5S)-6-Hydroxy-3,5-O-isopropylidene-3,5-dihydroxyhexanoate: Essential Building Block for HMG-CoA Reductase Inhibitors

Vanadium(II)‐ and Niobium(III)‐Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to Give a C₂‐Symmetrical HIV Protease Inhibitor

Efficient synthesis of (R)- and (S)-(6,6′-difluorobiphenyl-2,2′-diyl) bis(diphenylphosphine); electron-poor biphenyl-type ligands for transition metal catalysts.

Diastereo- and Enantioselective Synthesis of Ferrocenylphosphines by Twofold AsymmetricOrtho-Lithiation

Stereoselective synthesis of HR 780 a new highly potent HMG-CoA reductase inhibitor

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H. Jendralla

Practical Large Scale Synthesis of tert-Butyl (3R,5S)-6-Hydroxy-3,5-O-isopropylidene-3,5-dihydroxyhexanoate: Essential Building Block for HMG-CoA Reductase Inhibitors

Vanadium(II)‐ and Niobium(III)‐Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to Give a C2‐Symmetrical HIV Protease Inhibitor

Efficient synthesis of (R)- and (S)-(6,6′-difluorobiphenyl-2,2′-diyl) bis(diphenylphosphine); electron-poor biphenyl-type ligands for transition metal catalysts.

Diastereo- and Enantioselective Synthesis of Ferrocenylphosphines by Twofold AsymmetricOrtho-Lithiation

Stereoselective synthesis of HR 780 a new highly potent HMG-CoA reductase inhibitor

Contact Info

Product

Resources

About

Vanadium(II)‐ and Niobium(III)‐Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to Give a C₂‐Symmetrical HIV Protease Inhibitor