Author

Rochus Jonas

Observed names: R Jonas, R. JONAS, R. Jonas

Institutions: Merck KGaA, Darmstadt (Germany), Technische Universität Dresden

Observed institutions: National Institutes of Health, Merck KGaA, Darmstadt (Germany), National Institute on Aging, Technische Universität Dresden, Technische Universität Braunschweig

OpenAlex ID: A5020587011

The Two Mechanisms of Action of Racemic Cardiotonic EMD 53998, Calcium Sensitization and Phosphodiesterase Inhibition, Reside in Different Enantiomers

1993 · Inge Lues, Norbert Beier, et al. · Journal of Cardiovascular Pharmacology · 80

The Novel Cardiotonic Agent EMD 53 998 is a Potent “Calcium Sensitizer”

1991 · Norbert Beier, Juergen Harting, et al. · Journal of Cardiovascular Pharmacology · 65

Synthesis and biological activities of meribendan and related heterocyclic benzimidazolo-pyridazinones

1993 · R Jonas, M Klockow, et al. · European Journal of Medicinal Chemistry · 64

Novel diazinone derivatives separate myofilament Ca2+ sensitization and phosphodiesterase III inhibitory effects in guinea pig myocardium.

1992 · C Ventura, R Miller, et al. · Circulation Research · 35

Pharmacodynamic profile of the selective beta 1-adrenoceptor antagonist bisoprolol.

1986 · J Harting, K H Becker, et al. · PubMed · 26

Enantiomer Separation of a Novel Ca-Sensitizing Drug by simulated moving bed (SMB) - chromatography

1997 · Ralf M. Deveant, Rochus Jonas, et al. · Journal für praktische Chemie · 17

Preparation of the enantiomers of the novel CA-sensitizer EMD 53 998

1992 · R. Jonas, M. Klockow, et al. · Bioorganic & Medicinal Chemistry Letters · 16

Untersuchungen an hochsubstituierten Äthylenen und Glykolen, IV. Darstellung von hochsubstituierten Äthylenen mit Hilfe der Staudinger‐Pfenninger‐Reaktion

1966 · Hans Herloff Inhoffen, Rochus Jonas, et al. · Justus Liebig s Annalen der Chemie · 16

In Vivo Evidence of Positive Inotropism of EMD 57 033 Through Calcium Sensitization

1997 · Guenther Haeusler, Rochus Jonas, et al. · Journal of Cardiovascular Pharmacology · 15

Synthesis of a new type of ‘bent’ heterocyclic benzimidazolo-pyridazinones

1993 · R Jonas, H Prücher, et al. · European Journal of Medicinal Chemistry · 15

Imidazopyridines

1989 · P. Honerjäger, M. Klockow, et al. · Journal of Cardiovascular Pharmacology · 13

Stereoselectivity of the positive inotropic effects of newer diazinone-cardiotonics

1994 · R. Jonas, M. Klockow, et al. · Bioorganic & Medicinal Chemistry Letters · 8

Isomazol, Synthese der Enantiomeren

1986 · R. Jonas, H. Wurziger · Archiv der Pharmazie · 5

Three Thiadiazinone Derivatives, EMD 60417, EMD 66430, and EMD 66398, with Class III Antiarrhythmic Activity but Different Electrophysiologic Profiles

2001 · Herbert M. Himmel, Erich Wettwer, et al. · Journal of Cardiovascular Pharmacology · 4

Syntheses of (+)-and (-)-2-methoxy-4-(s-methyl-n-[(4-methylphenyl)-sulfonyl]-sulfonimidoyl)-benzoic acids and their absolute configurations

1987 · R. Jonas, H. Wurziger, et al. · Tetrahedron · 4

Organische Chemie 1998, Teil II

1999 · Michael Arlt, Henning Böttcher, et al. · Nachrichten aus Chemie Technik und Laboratorium

ChemInform Abstract: Synthesis of a New Type of “Bent” Heterocyclic Benzimidazolo‐ pyridazinones.

1993 · R. JONAS, H. PRUECHER, et al. · ChemInform

ChemInform Abstract: Synthesis and Biological Activities of Meribendan and Related Heterocyclic Benzimidazolo‐pyridazinones.

1993 · R. JONAS, M. KLOCKOW, et al. · ChemInform

ChemInform Abstract: Synthesis of (+)‐ and (‐)‐2‐Methoxy‐4‐(S‐methyl‐N‐((4‐methylphenyl)‐sulfonyl)‐sulfonimidoyl)‐benzoic Acids and Their Absolute Configurations.

1988 · R. JONAS, H. WURZIGER · ChemInform

ChemInform Abstract: Isomazole. Synthesis of the Enantiomers.

1987 · R. JONAS, H. WURZIGER · ChemInform

Works count: 20

Citation count: 383

H-index: 11

I10-index: 11