Wilhelm Bartmann - Concepedia

Author

Wilhelm Bartmann

Gesundes Kinzigtal (Germany)

Also Known As

W Bartmann, W. BARTMANN, W. Bartmann, Werner Bartmann, Wilhelm Bartmann, Wilhelm. Bartmann

Publications

845

Citations

H-Index

Concepts

All Affiliations

Gesundes Kinzigtal (Germany)Klinikum Frankfurt Höchst

About

Wilhelm Bartmann is an author at Gesundes Kinzigtal (Germany) specializing in pharmacology, biochemistry, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	10	10	312
2	Natural Sciences	8	8	243
3	Medicine	6	6	188
4	Engineering	1	1	24
5	Biomolecular Engineering	1	1	24

Wilhelm Bartmann

Publications

576

Citations

H-Index

Page 1

	Year	Citations
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
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
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
Prostacyclin and Synthetic Analogues Wilhelm Bartmann, Gerhard Beck Angewandte Chemie International Edition in English Cardiovascular PharmacologyPharmacotherapyHeterocycle ChemistryExperimental PharmacologyTranslational Pharmacology	1982	49
Modified bile acids: preparation of 7α,12α-dihydroxy-3β- and 7α,12α-dihydroxy-3α-(2-hydroxyethoxy)-5β-cholanic acid and their biological activity Günther Wess, Werner Kramer, Wilhelm Bartmann, Tetrahedron Letters Biological ActivityNatural Product SynthesisOxysterolBiochemistryBiliary Tract	1992	45
<b>Steroid Total Synthesis--Hydrochrysene Approach. XV.<sup>1</sup> Total Synthesis of Aldosterone</b> William S. Johnson, Joseph C. Collins, Raphael Pappo, Journal of the American Chemical Society Enantioselective SynthesisBiochemistryNatural SciencesAltmetric Attention ScoreXv.1 Total Synthesis	1963	40
Syntheses of 4(R)-silyloxy-6(S)-iodomethyl-tetrahydropyran-2-one and its enantiomer, building blocks for HMG-COA reductase inhibitors E. Baader, Wilhelm Bartmann, G. Beck, Tetrahedron Letters Building BlocksMedicinal ChemistryHmg-coa Reductase InhibitorsBiochemistryMedicine	1988	26
Convenient two-step stereospecific hydroxy-substitution with retention in β-hydroxy-δ-lactones. 4 ()-heterosubstituted mevinolin and -analogs Wilhelm Bartmann, G. Beck, E. Granzer, Tetrahedron Letters EngineeringOrganic ChemistryStereoselective SynthesisPharmacologySynthetic Chemistry	1986	24
Enantioselective synthesis of a new fluoro-substituted HMG-COA reductase inhibitor E. Baader, Wilhelm Bartmann, G. Beck, Tetrahedron Letters Medicinal ChemistryBiochemistryNatural SciencesFluorous SynthesisPharmaceutical Chemistry	1989	23

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