Year |
Citation |
Score |
2021 |
Hugelshofer CL, Bao J, Du J, Ashley E, Yu W, Ji T, Hu B, Liu D, Rondla R, Karampuri S, Sharma V, Ethiraj K, Lim YH. Scalable Preparation of 4,4-Disubstituted Six-Membered Cyclic Sulfones. Organic Letters. PMID 33417467 DOI: 10.1021/acs.orglett.0c04141 |
0.335 |
|
2019 |
Hugelshofer CL, Palani V, Sarpong R. Calyciphylline B-type Alkaloids: Evolution of a Synthetic Strategy to (-)-Daphlongamine H. The Journal of Organic Chemistry. PMID 31533427 DOI: 10.1021/Acs.Joc.9B02223 |
0.384 |
|
2019 |
Palani V, Hugelshofer CL, Sarpong R. A Unified Strategy for the Enantiospecific Total Synthesis of Delavatine A and Formal Synthesis of Incarviatone A. Journal of the American Chemical Society. PMID 31433634 DOI: 10.1021/Jacs.9B07693 |
0.464 |
|
2019 |
Hugelshofer CL, Palani V, Sarpong R. Calyciphylline B-Type Alkaloids: Total Syntheses of (-)-Daphlongamine H and (-)-Isodaphlongamine H. Journal of the American Chemical Society. PMID 31074980 DOI: 10.1021/Jacs.9B03576 |
0.351 |
|
2018 |
Hugelshofer CL, Palani V, Sarpong R. Oxazaborinines from Vinylogous N-Allylic Amides: Reactivities of Underexplored Heterocyclic Building Blocks. Organic Letters. PMID 29667837 DOI: 10.1021/Acs.Orglett.8B00859 |
0.314 |
|
2017 |
Hugelshofer CL, Magauer T. Dyotropic rearrangements in natural product total synthesis and biosynthesis. Natural Product Reports. PMID 28180228 DOI: 10.1039/C7Np00005G |
0.686 |
|
2016 |
Hugelshofer CL, Magauer T. Bioinspired total syntheses of terpenoids. Organic & Biomolecular Chemistry. PMID 27918058 DOI: 10.1039/C6Ob02488B |
0.64 |
|
2016 |
Hugelshofer CL, Magauer T. A Divergent Approach to the Marine Diterpenoids (+)-Dictyoxetane and (+)-Dolabellane V. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27601319 DOI: 10.1002/Chem.201603061 |
0.631 |
|
2016 |
Hugelshofer CL, Magauer T. A Bioinspired Cyclization Sequence Enables the Asymmetric Total Synthesis of Dictyoxetane. Journal of the American Chemical Society. PMID 27159010 DOI: 10.1021/Jacs.6B03720 |
0.646 |
|
2015 |
Hugelshofer CL, Magauer T. Total synthesis of the leucosceptroid family of natural products. Journal of the American Chemical Society. 137: 3807-10. PMID 25768917 DOI: 10.1021/Jacs.5B02021 |
0.659 |
|
2015 |
Hugelshofer CL, Magauer T. Strategies for the synthesis of antifeedant leucosceptroid natural products Synlett. 26. DOI: 10.1055/S-0034-1379964 |
0.69 |
|
2015 |
Hugelshofer CL, Magauer T. Total Synthesis of the Leucosceptroid Family of Natural Products Journal of the American Chemical Society. 137: 3807-3810. DOI: 10.1021/jacs.5b02021 |
0.651 |
|
2015 |
Hugelshofer CL, Magauer T. ChemInform Abstract: Strategies for the Synthesis of Antifeedant Leucosceptroid Natural Products Cheminform. 46: no-no. DOI: 10.1002/CHIN.201521261 |
0.468 |
|
2015 |
Hugelshofer CL, Magauer T. ChemInform Abstract: A General Entry to Antifeedant Sesterterpenoids: Total Synthesis of (+)-Norleucosceptroid A (I), (-)-Norleucosceptroid B (II), and (-)-Leucosceptroid K (III). Cheminform. 46: no-no. DOI: 10.1002/chin.201515264 |
0.585 |
|
2014 |
Luo SH, Hugelshofer CL, Hua J, Jing SX, Li CH, Liu Y, Li XN, Zhao X, Magauer T, Li SH. Unraveling the metabolic pathway in Leucosceptrum canum by isolation of new defensive leucosceptroid degradation products and biomimetic model synthesis. Organic Letters. 16: 6416-9. PMID 25474304 DOI: 10.1021/Ol503230S |
0.586 |
|
2014 |
Hugelshofer CL, Magauer T. A general entry to antifeedant sesterterpenoids: Total synthesis of (+)-norleucosceptroid A, (-)-norleucosceptroid B, and (-)-leucosceptroid K Angewandte Chemie - International Edition. 53: 11351-11355. PMID 25196778 DOI: 10.1002/Anie.201407788 |
0.689 |
|
2014 |
Hugelshofer CL, Magauer T. High-pressure transformations in natural product synthesis Synthesis (Germany). 46: 1279-1296. DOI: 10.1055/S-0033-1341073 |
0.602 |
|
2014 |
Hugelshofer CL, Magauer T. ChemInform Abstract: High-Pressure Transformations in Natural Product Synthesis Cheminform. 45: no-no. DOI: 10.1002/CHIN.201429261 |
0.35 |
|
2013 |
Hugelshofer CL, Mellem KT, Myers AG. Synthesis of quaternary α-methyl α-amino acids by asymmetric alkylation of pseudoephenamine alaninamide pivaldimine. Organic Letters. 15: 3134-7. PMID 23746325 DOI: 10.1021/Ol401337P |
0.464 |
|
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