| Year |
Citation |
Score |
| 2024 |
Bag S, Liu J, Patil S, Bonowski J, Koska S, Schölermann B, Zhang R, Wang L, Pahl A, Sievers S, Brieger L, Strohmann C, Ziegler S, Grigalunas M, Waldmann H. A divergent intermediate strategy yields biologically diverse pseudo-natural products. Nature Chemistry. PMID 38365941 DOI: 10.1038/s41557-024-01458-4 |
0.681 |
|
| 2023 |
Xie J, Pahl A, Krzyzanowski A, Krupp A, Liu J, Koska S, Schölermann B, Zhang R, Bonowski J, Sievers S, Strohmann C, Ziegler S, Grigalunas M, Waldmann H. Synthetic Matching of Complex Monoterpene Indole Alkaloid Chemical Space. Angewandte Chemie (International Ed. in English). e202310222. PMID 37818743 DOI: 10.1002/anie.202310222 |
0.538 |
|
| 2023 |
Aoyama H, Davies C, Liu J, Pahl A, Kirchhoff JL, Scheel R, Sievers S, Strohmann C, Grigalunas M, Waldmann H. Collective Synthesis of Sarpagine and Macroline Alkaloid-Inspired Compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). e202303027. PMID 37755456 DOI: 10.1002/chem.202303027 |
0.557 |
|
| 2023 |
Liu J, Zhang R, Mallick S, Patil S, Wientjens C, Flegel J, Krupp A, Strohmann C, Grassin C, Merten C, Pahl A, Grigalunas M, Waldmann H. A highly enantioselective intramolecular 1,3-dipolar cycloaddition yields novel pseudo-natural product inhibitors of the Hedgehog signalling pathway. Chemical Science. 14: 7936-7943. PMID 37502335 DOI: 10.1039/d3sc01240a |
0.561 |
|
| 2023 |
Liu J, Mallick S, Xie Y, Grassin C, Lucas B, Schölermann B, Pahl A, Scheel R, Strohmann C, Protzel C, Berg T, Merten C, Ziegler S, Waldmann H. Morphological profiling identifies the motor protein Eg5 as cellular target of spirooxindoles. Angewandte Chemie (International Ed. in English). e202301955. PMID 36929571 DOI: 10.1002/anie.202301955 |
0.554 |
|
| 2021 |
Waldmann H, Liu J, Flegel J, Otte F, Pahl A, Sievers S, Strohmann C. Combination of pseudo-natural product design and formal natural product ring distortion yields stereochemically and biologically diverse pseudo-sesquiterpenoid alkaloids. Angewandte Chemie (International Ed. in English). PMID 34297473 DOI: 10.1002/anie.202106654 |
0.581 |
|
| 2020 |
Waldmann H, Liu J, Cremosnik GS, Otte F, Pahl A, Sievers S, Strohmann C. Design, synthesis and biological evaluation of chemically and biologically diverse pyrroquinoline pseudo natural products. Angewandte Chemie (International Ed. in English). PMID 33200868 DOI: 10.1002/anie.202013731 |
0.544 |
|
| 2020 |
Cremosnik GS, Liu J, Waldmann H. Guided by evolution: from biology oriented synthesis to pseudo natural products. Natural Product Reports. PMID 33020792 DOI: 10.1039/d0np00015a |
0.533 |
|
| 2018 |
Ma D, Liu J. A unified approach for the assembly of atisine- and hetidine-type diterpenoid alkaloids: Total syntheses of azitine and the proposed structure of navirine C. Angewandte Chemie (International Ed. in English). PMID 29611891 DOI: 10.1002/Anie.201803018 |
0.439 |
|
| 2016 |
Zhang H, Liu R, Liu J, Li L, Wang P, Yao SQ, Xu Z, Sun H. A minimalist fluorescent probe for differentiating Cys, Hcy and GSH in live cells. Chemical Science. 7: 256-260. PMID 28758002 DOI: 10.1039/C5Sc02431E |
0.379 |
|
| 2015 |
Guo S, Liu J, Ma D. Total synthesis of leucosceptroids A and B. Angewandte Chemie (International Ed. in English). 54: 1298-301. PMID 25470240 DOI: 10.1002/Anie.201410134 |
0.42 |
|
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