Heiner Jendralla - Concepedia

Author

Heiner Jendralla

Klinikum Frankfurt Höchst

Also Known As

H Jendralla, H. JENDRALLA, H. Jendralla, Heiner Jendralla, Heiner. Jendralla, Jendralla Heiner

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Klinikum Frankfurt Höchst Gesundes Kinzigtal (Germany)

About

Heiner Jendralla is an author at Klinikum Frankfurt Höchst specializing in natural sciences, medicinal chemistry, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	13	16	484
2	Biochemistry	11	13	428
3	Medicine	10	10	361
4	Engineering	9	9	210
5	Biomolecular Engineering	6	6	115

Heiner Jendralla

Publications

855

Citations

H-Index

Page 1

	Year	Citations
Vanadium(<scp>II</scp>)‐ and Niobium(<scp>III</scp>)‐Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to <i>C</i><sub>2</sub>‐Symmetrical HIV‐Protease Inhibitors Bernhard Kammermeier, Gerhard Beck, Heiner Jendralla, Angewandte Chemie International Edition in English Combinatorial ChemistryMolecular BiologyOrganic ChemistryPeptide ScienceChemical Biology	1994	74
Synthesis and biological activity of new HMG-CoA reductase inhibitors. 1. Lactones of pyridine- and pyrimidine-substituted 3,5-dihydroxy-6-heptenoic (-heptanoic) acids G. Beck, E. Baader, Wilhelm Bartmann, Journal of Medicinal Chemistry	1990	68
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 Gerhard Beck, Heiner Jendralla Synthesis Medicinal ChemistryHmg-coa Reductase InhibitorsBiochemistryNatural SciencesMedicine	1995	68
Stereoselective synthesis of HR 780 a new highly potent HMG-CoA reductase inhibitor Günther Wess, E. Baader, Wilhelm Bartmann, Tetrahedron Letters Medicinal ChemistryBiochemistryMedicineNatural SciencesPharmacotherapy	1990	65
Synthesis and biological activity of new HMG-CoA reductase inhibitors. 2. Derivatives of 7-(1H-pyrrol-3-yl)-substituted-3,5-dihydroxyhept-6(E)-enoic (-heptanoic) acids Heiner Jendralla, E. Baader, Wilhelm Bartmann, Journal of Medicinal Chemistry	1990	64
Efficient synthesis of (R)- and (S)-(6,6′-difluorobiphenyl-2,2′-diyl) bis(diphenylphosphine); electron-poor biphenyl-type ligands for transition metal catalysts. Heiner Jendralla, Chang Hua Li, Erich F. Paulus Tetrahedron Asymmetry Chemical EngineeringEngineeringOrganometallic CatalysisCatalysisTransition Metal Catalysts	1994	59
Vanadium(<scp>II</scp>)‐ and Niobium(<scp>III</scp>)‐Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to Give a <i>C</i><sub>2</sub>‐Symmetrical HIV Protease Inhibitor Bernhard Kammermeier, Gerhard Beck, Wolfgang Holla, Chemistry - A European Journal Vanadium Complex 11Bioorganic ChemistryPeptide ScienceMedicinal ChemistryStereoselective Synthesis	1996	52
Synthesis and biological activity of new HMG-CoA reductase inhibitors. 3. Lactones of 6-phenoxy-3,5-dihydroxyhexanoic acids Heiner Jendralla, E. Granzer, B. v. Kerékjártó, Journal of Medicinal Chemistry	1991	51
Diastereo- and Enantioselective Synthesis of Ferrocenylphosphines by Twofold Asymmetric<i>Ortho</i>-Lithiation Heiner Jendralla, Erich F. Paulus Synlett Asymmetric CatalysisEngineeringPure Monophosphine 1HMeso-diphosphine 1JOrganic Chemistry	1997	37
Asymmetric hydrogenation of itaconic acids with rhodium(I)-phenyl-capp complex a correction Heiner Jendralla Tetrahedron Letters BiochemistryNatural SciencesProton TransferOrganometallic CatalysisHomogeneous Catalysis	1991	32

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