Olaf Schupp - Concepedia

Author

Olaf Schupp

University of Würzburg

Also Known As

O. E. Schupp, O. SCHUPP, O. Schupp, O. Schupp, Jr., O.E. Schupp, Olaf Schupp, Schupp, O., О. Schupp

Publications

671

Citations

H-Index

Concepts

All Affiliations

University of Würzburg Max Planck Institute for Solid State Research Omar Bongo University University of Milan

About

Olaf Schupp is an author at University of Würzburg specializing in organic chemistry, chemistry, and biomolecular engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	8	8	229
2	Biomolecular Engineering	8	8	229
3	Natural Sciences	6	6	272
4	Biochemistry	3	3	146
5	Medicine	1	1	22

Olaf Schupp

Publications

503

Citations

H-Index

Page 1

	Year	Citations
The Stereochemistry of the Phosphonate Modification of the Wittig Reaction D. H. WADSWORTH, Olaf Schupp, Edward J. Seus, The Journal of Organic Chemistry Phosphonate ModificationBioorganic ChemistryChemical MeasurementBiochemistryChemical Analysis	1965	110
Atropisomerization Barriers of Configurationally Unstable Biaryl Compounds, Useful Substrates for Atroposelective Conversions to Axially Chiral Biaryls Gerhard Bringmann, Markus Heubes, Matthias Breuning, The Journal of Organic Chemistry	2000	71
Novel Concepts in Directed Biaryl Synthesis, IX. Synthesis and Structure of Benzonaphthopyranones, Useful Bridged Model Precursors for Stereoselective Biaryl Syntheses Gerhard Bringmann, Thomas Härtung, Lothar Göbel, Liebigs Annalen der Chemie Cross-coupling ReactionEngineeringMolecular DistortionNatural SciencesLactones 7	1992	65
Yb(OTf)<sub>3</sub>-Catalyzed One-Pot Synthesis of β-Lactams from Silyl Ketene Thioacetals by a Two- or a Three-Component Reaction Rita Annunziata, Mauro Cinquini, Franco Cozzi, The Journal of Organic Chemistry EngineeringItaly CiteSilyl Ketene ThioacetalsDiversity-oriented SynthesisOne-pot Synthesis	1996	39
Cis- and trans-isoshinanolone from Dioncophyllum thollonii: absolute configuration of two `known', wide-spread natural products1Part 127 in the series `Acetogenic isoquinoline alkaloids'. For part 126, see Bringmann et al., submitted for publication (a).1 Gerhard Bringmann, Miriam Münchbach, Kim Messer, Phytochemistry Absolute ConfigurationPart 126Secondary MetaboliteAcetogenic Isoquinoline AlkaloidsPhytochemistry	1999	31
A new multicomponent synthesis of 1,2,3,4-tetrahydroquinolines Rita Annunziata, Mauro Cinquini, Franco Cozzi, Tetrahedron Combinatorial ChemistryOrganic ChemistryNew Multicomponent SynthesisChemistryHeterocycle Chemistry	1997	30
Novel concepts in directed biaryl synthesis, XXXIV. Synthesis, optical resolution, and helimerization of dinaphtho[2,1‐<i>b</i>:1′,2′‐<i>d</i>]‐pyran‐4‐one Gerhard Bringmann, Bernd Schöner, Olaf Schupp, Liebigs Annalen der Chemie EngineeringActivation ParametersOrganic ChemistryChemistryHeterocycle Chemistry	1994	26
Stereoselective one-pot synthesis of β-lactams by Lewis acid promoted condensation of silylketene thioacetals with imines Rita Annunziata, Mauro Cinquini, Franco Cozzi, Tetrahedron Stereoselective One-pot SynthesisEngineeringLewis AcidOrganic ChemistrySilylketene Thioacetals	1996	25
Acetogenic isoquinoline alkaloids Gerhard Bringmann, Markus Rückert, Kim Messer, Journal of Chromatography A Natural Product SynthesisActive IngredientMedicineHerb-drug InteractionAcetogenic Isoquinoline Alkaloids	1999	22
Novel Concepts in Directed Biaryl Synthesis, XVI. Synthesis and Structure of Benzonaphthopyrans; Helically Distorted, Bridged Biaryls with Different Steric Hindrance at the Axis Gerhard Bringmann, Thomas Härtung, Lothar Göbel, Liebigs Annalen der Chemie EngineeringNmr SpectroscopyNatural SciencesDiversity-oriented SynthesisBiaryls 3	1992	22

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