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Birgit Werner

Researcher at Ludwig Maximilian University of Munich

Publications -  9
Citations -  374

Birgit Werner is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: Ether & Carborane. The author has an hindex of 6, co-authored 9 publications receiving 361 citations. Previous affiliations of Birgit Werner include Technische Universität München.

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Since 1995 the new chemistry of multicomponent reactions and their libraries, including their heterocyclic chemistry

Ivar Ugi, +2 more
- 01 May 2000 - 
TL;DR: A growing number of products, including many heterocycles, can be prepared by the one-pot MultiComponent Reactions (MCRs) just by mixing three or more educts, and in many cases practically quantitative yields of pure products can be obtained as mentioned in this paper.
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Single-Chain Polyprenyl Phosphates Form “Primitive” Membranes

Gianluca Pozzi, +6 more
- 02 Feb 1996 - 
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New carborane-based compounds for boron neutron capture therapy: binding and toxicity of ANC-1, DAC-1 and B-Et-11-OMe in cultured human glioma and mouse melanoma cells.

Peter Lindström, +8 more
- 01 Feb 1994 - 
TL;DR: The toxicity and binding of the three new carborane based compounds, DAC, B-Et-11-OMe and BSH, and the previously developed compound di-sodium undecahydro-mercapto-closo-dodecarborate were analyzed with cultured human glioma cells and mouse melanoma cells as biological models.
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Five-Membered Cyclic Phosphorylating Reagents and Related Compounds

Peter Lemmen, +5 more
- 01 Jan 1993 - 
TL;DR: In this article, the conceptual and mechanistic basis for five-membered cyclic phosphorylating reagents and related compounds is discussed, as well as a selection of typical results.
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Synthesis of rac-1-(9-o-carboranyl)nonyl-2-methyl-glycero-3-phosphocholine (B-Et-11-OMe), a potential boron carrier for Boron Neutron Capture Therapy (BNCT)

Peter Lemmen, +1 more
- 01 Sep 1992 - 
TL;DR: In this article, carborane is introduced into the readily assembled glycerol ether moiety and the phosphocholine headgroup is introduced by 2-chloro-3-methyl-1,3,2-λ3-oxazaphospholane using a phosphoamidite strategy and subsequent ring opening under alkylating conditions.