Alexander Dömling

Prof. Dr. Alexander Dömling

Department of Drug Design, University of Groningen, Groningen, The Netherlands
orcid

Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 December 2005 in Chemical Reviews
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Journal Article
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ADAlexander Dömling
Alexander Dömling

13 September 2000
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Journal Article
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PDF file
ADAlexander Dömling
Alexander Dömling
IUIvar Ugi
Ivar Ugi

22 March 2012 in Chemical Reviews
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Journal Article
Closed access
ADAlexander Dömling
Alexander Dömling
WWwei wang
wei wang
KWKan Wang
Kan Wang

1 February 2019 in Chemical Reviews
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Journal Article
Open access
CNConstantinos G. Neochoritis
Constantinos G. Neochoritis
TZTing Zhao
Ting Zhao
ADAlexander Dömling
Alexander Dömling
Tetrazole derivatives are a prime class of heterocycles, very important to medicinal chemistry and drug design due to not only their bioisosterism to carboxylic acid and amide moieties but also to their metabolic stability and other beneficial physicochemical properties. Although more than 20 FDA-approved drugs contain 1H- or 2H-tetrazole substituents, their exact binding mode, structural biology, 3D conformations, and in general their chemical behavior is not fully understood. Importantly, multicomponent reaction (MCR) chemistry offers convergent access to multiple tetrazole scaffolds providing the three important elements of novelty, diversity, and complexity, yet MCR pathways to tetrazoles are far from completely explored. Here, we review the use of multicomponent reactions for the preparation of substituted tetrazole derivatives. We highlight specific applications and general trends holding therein and discuss synthetic approaches and their value by analyzing scope and limitations, and also enlighten their receptor binding mode. Finally, we estimated the prospects of further research in this field.

1 June 2002 in Current Opinion in Chemical Biology
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Journal Article
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ADAlexander Dömling
Alexander Dömling

31 January 2003 in Molecules
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Journal Article
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IUI. Ugi
I. Ugi
BWB. Werner
B. Werner
ADAlexander Dömling
Alexander Dömling
The first century of isocyanide chemistry, which was then still a rather empty part of Organic Chemistry, began in 1859. In 1958 isocyanides became generally available by dehydration the formylamines. One year later the four component reaction of isocyanides (U-4CR) was introduced. This one-pot reaction is accomplished just by mixing amines, carbonyl compounds, suitable acids and isocyanides. Most chemical reactions have their own ”scope and limitation”, whereas the U-4CR can convert almost all combinations of educts into their products. Until 1995 this chemistry was moderately used, but since then a new era of the U-4CR and its unions with further reactions have become increasingly popular, particularly as libraries. In industry this chemistry became one of its most often used methods of finding new desirable products. In contrast to most other areas of chemistry, isocyanide chemistry is not yet exhausted and still much progress can be expected there.