Dieter Enders

734 citations

25 papers · 560 indexed · h-index 13

Organic Chemistry top 5%
- Asymmetric Synthesis and Catalysis 7
- Synthetic Organic Chemistry Methods 5
- Axial and Atropisomeric Chirality Synthesis 4
- Organophosphorus compounds synthesis 3
- Chemical Synthesis and Reactions 3
- Coordination Chemistry and Organometallics 3
- Carbohydrate Chemistry and Synthesis 2
Biochemistry top 10%
Inorganic Chemistry top 10%
Pharmaceutical Science
- Fluorine in Organic Chemistry 2
Spectroscopy

Co-authors: Herbert Eichenauer Jan W. Bats Mark G. Bock E. J. Corey Livio Tedeschi Johannes Köbberling Stefan Bräse Matthieu Jeanty
Cited by: Organic Chemistry Biochemistry Inorganic Chemistry
Journals: Angewandte Chemie International Edition (3 papers)FEBS Letters (1 paper)Tetrahedron Letters (3 papers)
Partner nations: Germany Poland France

In The Last Decade

Dieter Enders

25 papers receiving 522 citations

Peers

Countries citing papers authored by Dieter Enders

Since Specialization

Citations

This map shows the geographic impact of Dieter Enders'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 Dieter Enders with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dieter Enders more than expected).

Fields of papers citing papers by Dieter Enders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dieter Enders. 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 Dieter Enders. The network helps show where Dieter Enders may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Dieter Enders, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Dieter Enders Line = papers co-authored together Dieter Enders links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Mono- und ditope Rezeptoren: Synthese, Bindungsstudien und kooperative Effekte RWTH Publications (RWTH Aachen) ·Jan Alexander Stubenrauch,Markus Albrecht,Dieter Enders	2015	1
2	Asymmetric Synthesis of Functionalized Dihydro- and Tetrahydropyrans via an Organocatalytic Domino Michael–Hemiacetalization Reaction Synthesis ·Dieter Enders,Gregor Urbanietz,Iuliana Atodiresei	2014	22
3	Asymmetric Synthesis of 3-Substituted Hexahydro-3H-isochromenes via an Organocatalytic Triple Cascade/Yb-Catalyzed Hetero-Diels-Alder Sequence Synthesis ·Dieter Enders,Nico Erdmann,Iuliana Atodiresei	2012	3
4	Organocatalytic Asymmetric Triple Domino Reactions of Nitromethane with α,β-Unsaturated Aldehydes Synlett ·Dieter Enders,Matthieu Jeanty,Jan W. Bats	2009	30
5	Asymmetrische organokatalytische de novo Synthese von Kohlenhydraten, Phytosphingosinen und 1-epi-(+)MK7607 RWTH Publications (RWTH Aachen) ·Christoph Bernhard Grondal,Dieter Enders	2006	1
6	Characterisation of plant tocopherol cyclases and their overexpression in transgenic Brassica napus seeds FEBS Letters ·Rajeev Kumar,Mirela Raclaru,Thomas Schüßeler,Jens Gruber,Radin Sadre,Wilfried Lühs,Karim Zarhloul,W. Friedt,Dieter Enders,Margrit Frentzen,Dagmar Weier	2005	60
7	Efficient Asymmetric Syntheses of (+)‐Strictifolione. ChemInform ·Dieter Enders,Achim Lenzen,Michael Mueller	2004	1
8	The First Highly Efficient Asymmetric Synthesis of α-Substituted Methyl Sulfonates Angewandte Chemie International Edition ·Dieter Enders,Nicola Vignola,Otto Mathias Berner,Jan W. Bats	2002	24
9	Efficient asymmetric synthesis of ?-alkylated 1,4-cyclohexanedione derivatives, important chiral building blocks in the synthesis of natural products Chirality ·Dieter Enders,Anja N�hring,Jan Runsink	2000	12
10	Asymmetric Synthesis ofα-Substitutedβ-Nitrophosphonic Acids by Phospha-Analogous Michael Addition to Aromatic Nitroalkenes Angewandte Chemie International Edition ·Dieter Enders,Livio Tedeschi,Jan W. Bats	2000	62
11	ChemInform Abstract: Triazenes: A Useful Protecting Strategy for Sensitive Secondary Amines. ChemInform ·Ryszard Łaźny,Janusz Popławski,Johannes Koebberling,Dieter Enders,Stefan Braese	1999	1
12	A Surprising Solid-Phase Effect: Development of a Recyclable “Traceless” Linker System for Reactions on Solid Support Angewandte Chemie International Edition ·Stefan Bräse,Dieter Enders,Johannes Köbberling,Frank Avemaria	1998	76
13	Organic Synthesis via Organometallics (OSM 4) Dieter Enders,Hans‐Joachim Gais,Wilhelm Keim,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unkn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14	Organic synthesis via organometallics (OSM 4) : proceedings of the fourth symposium in Aachen, July 15 to 18, 1992 Dieter Enders,Hans‐Joachim Gais,Wilhelm Keim	1993	1
15	C-C - connective synthesis of α-dialkylamino - ketones from aldehydes and sec.-amines Tetrahedron Letters ·Dieter Enders,Hermann Lotter	1982	18
16	Photoelectron-spectra and conformational behavior of hydrazones Journal of Chemical Research Synopses ·Paul Rademacher,H. Eichenauer,Peter Weuster,Dieter Enders,H Pfeffer	1979	3
17	Asymmetrische Synthese von Ameisen‐Alarmpheromonen – α‐Alkylierung von acyclischen Ketonen mit praktisch vollständiger asymmetrischer Induktion Angewandte Chemie ·Dieter Enders,Herbert Eichenauer	1979	22
18	NMR-spektroskopische untersuchungen an deprotonierten iminen und hydrazonen Tetrahedron Letters ·H. AHLBRECHT,Ernst O. Düber,Dieter Enders,Herbert Eichenauer,Peuter Weuster	1978	20
19	A simple and highly effective route to α,β-unsaturated aldehydes Tetrahedron Letters ·E. J. Corey,Dieter Enders,Mark G. Bock	1976	103
20	Metallierung am primären, sekundären und tertiären C‐Atom offenkettiger und cyclischer Nitrosamine Angewandte Chemie ·Dieter Seebàch,Dieter Enders	1972	5

About Dieter Enders

Dieter Enders is a scholar working on Organic Chemistry, Pharmaceutical Science and Physical and Theoretical Chemistry, having authored 25 papers that have together received 560 indexed citations. Recurring topics across this work include Asymmetric Synthesis and Catalysis (7 papers), Synthetic Organic Chemistry Methods (5 papers), Axial and Atropisomeric Chirality Synthesis (4 papers), Organophosphorus compounds synthesis (3 papers), Chemical Synthesis and Reactions (3 papers), Coordination Chemistry and Organometallics (3 papers), Carbohydrate Chemistry and Synthesis (2 papers) and Fluorine in Organic Chemistry (2 papers). The work is most often cited by research in Organic Chemistry (455 citations), Biochemistry (43 citations) and Inorganic Chemistry (92 citations). Dieter Enders has collaborated with scholars based in Germany, Poland and France. Frequent co-authors include Herbert Eichenauer, Jan W. Bats, Mark G. Bock, E. J. Corey, Livio Tedeschi, Johannes Köbberling, Stefan Bräse, Matthieu Jeanty, Iuliana Atodiresei and Hermann Lotter. Their work appears in journals such as Angewandte Chemie International Edition, FEBS Letters and Tetrahedron Letters.

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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