Martin Eberle - Concepedia

Author

Martin Eberle

Novartis (Switzerland)ORCID

Also Known As

Eberle, Martin, M. EBERLE, M. Eberle, Martin Eberle, Martin. Eberle

Publications

851

Citations

H-Index

Concepts

All Affiliations

Novartis (Switzerland)University of Tübingen ETH Zurich École Polytechnique Fédérale de Lausanne Hunan University

About

Martin Eberle is an author at Novartis (Switzerland) specializing in engineering, organic chemistry, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	9	9	439
2	Natural Sciences	6	6	362
3	Applied Physics	2	2	34
4	Medicine	1	1	15
5	Public Health	1	1	10

Martin Eberle

Publications

810

Citations

H-Index

Page 1

	Year	Citations
Batch versus Flow Photochemistry: A Revealing Comparison of Yield and Productivity Luke D. Elliott, Jonathan P. Knowles, Paul J. Koovits, Chemistry - A European Journal	2014	206
A Collection of Robust Organic Synthesis Reactions for <i>In Silico</i> Molecule Design Markus Hartenfeller, Martin Eberle, Peter Meier, Journal of Chemical Information and Modeling Combinatorial ChemistryFocused CollectionMedicinal ChemistryBioorganic ChemistryEngineering	2011	119
[3 + 3]-Carbocyclizations of nitroallylic esters and enamines with stereoselective formation of up to six new stereogenic centers Dieter Seebàch, Martin Missbach, Giorgio Calderari, Journal of the American Chemical Society Molecular SciencesEngineeringHeterocyclicBiochemistryStereoselective Formation	1990	98
Absolute Konfiguration des Mevalolactons Martin Eberle, D. Arigoni Helvetica Chimica Acta Integral GeometryFrenchBioorganic ChemistryQuinic AcidEngineering	1960	56
Molecular yardsticks. Synthesis of extended equilibrium transfer alkylating cross-link reagents and their use in the formation of macrocycles Stephen Brocchini, Martin Eberle, Richard Lawton Journal of the American Chemical Society Combinatorial ChemistryCross-coupling ReactionMolecular SciencesEngineeringMolecular Yardsticks	1988	52
Enantioselektive Verseifung der Diacetate von 2‐Nitro‐1,3‐diolen mit Schweineleber‐Esterase und Herstellung enantiomerenreiner Derivate von 2‐Nitro‐allylalkoholen (chirale Verknüpfungsreagenzien) Martin Eberle, Martin Egli, Dieter Seebàch Helvetica Chimica Acta Bioorganic ChemistryBiochemistryNatural SciencesCyclic DiacetatesOrganic Chemistry	1988	51
(<i>R</i>)-Ethyl 4-<i>t</i>-Butoxy-3-hydroxybutanoate, a Versatile Chiral Building Block for EPC (Enantiomerically Pure Compound) Syntheses, by Yeast Reduction of Ethyl 4-<i>t</i>-Butoxy-3-oxobutanoate Dieter Seebàch, Martin Eberle Synthesis Engineering-Malic AcidOrganic ChemistryEnzymatic ModificationEnantiomerically Pure Compound	1986	49
Probing the Bioactivity-Relevant Chemical Space of Robust Reactions and Common Molecular Building Blocks Markus Hartenfeller, Martin Eberle, Peter Meier, Journal of Chemical Information and Modeling	2012	40
Thioalkylation of <i>Meldrum</i>'s Acid: Protected alkylidene derivatives of isopropylidene malonate Martin Eberle, Richard Lawton Helvetica Chimica Acta Derivative (Chemistry)DerivativesEngineeringBiochemistryParent Olefin	1988	21
Picosecond electrical response in graphene/MoTe2 heterojunction with high responsivity in the near infrared region Zhouxiaosong Zeng, Kai Braun, Cuihuan Ge, Fundamental Research	2021	20

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