5 article(s) from Wessjohann, Ludger A
Synthesis of a tubugi-1-toxin conjugate by a modulizable disulfide linker system with a neuropeptide Y analogue showing selectivity for hY1R-overexpressing tumor cells
- Rainer Kufka,
- Robert Rennert,
- Goran N. Kaluđerović,
- Lutz Weber,
- Wolfgang Richter and
- Ludger A. Wessjohann
Beilstein J. Org. Chem. 2019, 15, 96–105, doi:10.3762/bjoc.15.11
Synthesis of antibacterial 1,3-diyne-linked peptoids from an Ugi-4CR/Glaser coupling approach
- Martin C. N. Brauer,
- Ricardo A. W. Neves Filho,
- Bernhard Westermann,
- Ramona Heinke and
- Ludger A. Wessjohann
Beilstein J. Org. Chem. 2015, 11, 25–30, doi:10.3762/bjoc.11.4
Consecutive isocyanide-based multicomponent reactions: synthesis of cyclic pentadepsipeptoids
- Angélica de Fátima S. Barreto,
- Otilie E. Vercillo,
- Ludger A. Wessjohann and
- Carlos Kleber Z. Andrade
Beilstein J. Org. Chem. 2014, 10, 1017–1022, doi:10.3762/bjoc.10.101
The multicomponent approach to N-methyl peptides: total synthesis of antibacterial (–)-viridic acid and analogues
- Ricardo A. W. Neves Filho,
- Sebastian Stark,
- Bernhard Westermann and
- Ludger A. Wessjohann
Beilstein J. Org. Chem. 2012, 8, 2085–2090, doi:10.3762/bjoc.8.234
Synthesis of (−)-julocrotine and a diversity oriented Ugi-approach to analogues and probes
- Ricardo A. W. Neves Filho,
- Bernhard Westermann and
- Ludger A. Wessjohann
Beilstein J. Org. Chem. 2011, 7, 1504–1507, doi:10.3762/bjoc.7.175
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