Christian Herber

484 total citations
9 papers, 422 citations indexed

About

Christian Herber is a scholar working on Organic Chemistry, Molecular Biology and Biotechnology. According to data from OpenAlex, Christian Herber has authored 9 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Organic Chemistry, 3 papers in Molecular Biology and 3 papers in Biotechnology. Recurrent topics in Christian Herber's work include Asymmetric Synthesis and Catalysis (6 papers), Synthetic Organic Chemistry Methods (4 papers) and Chemical Synthesis and Analysis (3 papers). Christian Herber is often cited by papers focused on Asymmetric Synthesis and Catalysis (6 papers), Synthetic Organic Chemistry Methods (4 papers) and Chemical Synthesis and Analysis (3 papers). Christian Herber collaborates with scholars based in Germany and United Kingdom. Christian Herber's co-authors include Bernhard Breit, Stephen T. Liddle, S. Fabre, Caroline M. Dick, R.A. Coxall, Philip J. Bailey, Andrew Parkin, Simon Parsons, David R. J. Hose and Alan Steven and has published in prestigious journals such as Angewandte Chemie International Edition, Chemistry - A European Journal and Synthesis.

In The Last Decade

Christian Herber

9 papers receiving 410 citations

Peers

Christian Herber

OC

IC

MB

MC

PHARM

Martin Bindl Germany

P. SCHNURRENBERGER Switzerland

Christie Morrill United States

Raymond E. Forslund United States

Jan H. Kirchhoff United States

Michael H. Wu United States

Nikhil Chowdhury India

Naohiro Kirai Japan

Douglas A. Engel United States

Mei‐Huey Lin Taiwan

Martin Bindl Germany

Christian Herber

286 ×0.8

OC

89 ×0.8

IC

89 ×0.9

MB

44 ×1.4

MC

37 ×1.3

PHARM

Citations per year, relative to Christian Herber Christian Herber (= 1×) peers Martin Bindl

Countries citing papers authored by Christian Herber

Since Specialization

Citations

This map shows the geographic impact of Christian Herber's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Christian Herber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christian Herber more than expected).

Fields of papers citing papers by Christian Herber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christian Herber. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Christian Herber. The network helps show where Christian Herber may publish in the future.

Co-authorship network of co-authors of Christian Herber

This figure shows the co-authorship network connecting the top 25 collaborators of Christian Herber. A scholar is included among the top collaborators of Christian Herber based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Christian Herber. Christian Herber is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

1.

Hose, David R. J., et al.. (2018). Redesign of the Synthesis and Manufacture of an Azetidine-Bearing Pyrazine. Organic Process Research & Development. 22(2). 241–246. 9 indexed citations

2.

Breit, Bernhard, et al.. (2010). Economic Large-Scale Synthesis of o- and m-Diphenylphosphinobenzoic Acids. Synthesis. 2010(11). 1924–1928. 1 indexed citations

3.

Herber, Christian & Bernhard Breit. (2007). Enantioselective Total Synthesis and Determination of the Absolute Configuration of the 4,6,8,10,16,18‐Hexamethyldocosane from Antitrogus parvulus. European Journal of Organic Chemistry. 2007(21). 3512–3519. 45 indexed citations

4.

Herber, Christian & Bernhard Breit. (2006). Iterative Deoxypropionate Synthesis Based on a Copper‐Mediated Directed Allylic Substitution: Formal Total Synthesis of Borrelidin (C3–C11 Fragment). Chemistry - A European Journal. 12(25). 6684–6691. 45 indexed citations

5.

Herber, Christian & Bernhard Breit. (2005). Enantioselective Total Synthesis and Determination of the Absolute Configuration of the 4,6,8,10,16,18‐Hexamethyldocosane from Antitrogus parvulus. Angewandte Chemie. 117(33). 5401–5403. 33 indexed citations

6.

Herber, Christian & Bernhard Breit. (2005). Enantioselective Total Synthesis and Determination of the Absolute Configuration of the 4,6,8,10,16,18‐Hexamethyldocosane from Antitrogus parvulus. Angewandte Chemie International Edition. 44(33). 5267–5269. 54 indexed citations

7.

Breit, Bernhard & Christian Herber. (2004). Iterative Desoxypropionat‐Synthese auf der Basis einer kupfervermittelten dirigierten allylischen Substitution. Angewandte Chemie. 116(29). 3878–3880. 40 indexed citations

8.

Breit, Bernhard & Christian Herber. (2004). Iterative Deoxypropionate Synthesis Based on a Copper‐Mediated Directed Allylic Substitution. Angewandte Chemie International Edition. 43(29). 3790–3792. 53 indexed citations

9.

Bailey, Philip J., R.A. Coxall, Caroline M. Dick, et al.. (2003). The First Structural Characterisation of a Group 2 Metal Alkylperoxide Complex: Comments on the Cleavage of Dioxygen by Magnesium Alkyl Complexes. Chemistry - A European Journal. 9(19). 4820–4828. 142 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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