Year |
Citation |
Score |
2017 |
Lagoutte R, Serba C, Winssinger N. Synthesis of deoxyelephantopin analogues. The Journal of Antibiotics. PMID 29089602 DOI: 10.1038/Ja.2017.132 |
0.703 |
|
2016 |
Lagoutte R, Serba C, Abegg D, Hoch DG, Adibekian A, Winssinger N. Divergent synthesis and identification of the cellular targets of deoxyelephantopins. Nature Communications. 7: 12470. PMID 27539788 DOI: 10.1038/Ncomms12470 |
0.713 |
|
2016 |
Serba C, Lagoutte R, Winssinger N. Rapid and Scalable Synthesis of cis-Fused Guaiane-Type Sesquiterpenes European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201501277 |
0.726 |
|
2014 |
Duplan V, Serba C, Garcia J, Valot G, Barluenga S, Hoerlé M, Cuendet M, Winssinger N. Synthesis of sesquiterpene-inspired derivatives designed for covalent binding and their inhibition of the NF-κB pathway. Organic & Biomolecular Chemistry. 12: 370-5. PMID 24263232 DOI: 10.1039/C3Ob42049C |
0.635 |
|
2013 |
Novoa A, Barluenga S, Serba C, Winssinger N. Solid phase synthesis of glycopeptides using Shoda's activation of unprotected carbohydrates. Chemical Communications (Cambridge, England). 49: 7608-10. PMID 23882465 DOI: 10.1039/C3Cc43458C |
0.733 |
|
2013 |
Serba C, Winssinger N. Following the Lead from Nature: Divergent Pathways in Natural Product Synthesis and Diversity-Oriented Synthesis (Eur. J. Org. Chem. 20/2013) European Journal of Organic Chemistry. 2013: n/a-n/a. DOI: 10.1002/Ejoc.201390055 |
0.628 |
|
2013 |
Serba C, Winssinger N. Following the lead from nature: Divergent pathways in natural product synthesis and diversity-oriented synthesis European Journal of Organic Chemistry. 4195-4214. DOI: 10.1002/Ejoc.201300201 |
0.615 |
|
2013 |
Serba C, Winssinger N. ChemInform Abstract: Following the Lead from Nature: Divergent Pathways in Natural Product Synthesis and Diversity-Oriented Synthesis. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201343221 |
0.426 |
|
2012 |
Valot G, Garcia J, Duplan V, Serba C, Barluenga S, Winssinger N. Diversity-oriented synthesis of diverse polycyclic scaffolds inspired by the logic of sesquiterpene lactones biosynthesis. Angewandte Chemie (International Ed. in English). 51: 5391-4. PMID 22517777 DOI: 10.1002/Anie.201201157 |
0.632 |
|
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