Year |
Citation |
Score |
2018 |
Kearney SE, Zahoránszky-Kőhalmi G, Brimacombe KR, Henderson MJ, Lynch C, Zhao T, Wan KK, Itkin Z, Dillon C, Shen M, Cheff DM, Lee TD, Bougie D, Cheng K, Coussens NP, ... ... Moreno J, et al. Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space. Acs Central Science. 4: 1727-1741. PMID 30648156 DOI: 10.1021/Acscentsci.8B00747 |
0.725 |
|
2018 |
Picazo E, Morrill LA, Susick R, Moreno J, Smith J, Garg NK. Enantioselective Total Syntheses of Methanoquinolizidine-Containing Akuammiline Alkaloids and Related Studies. Journal of the American Chemical Society. PMID 29694031 DOI: 10.1021/Jacs.8B03404 |
0.768 |
|
2017 |
Medina JM, Moreno J, Racine S, Du S, Garg NK. Mizoroki-Heck Cyclizations of Amide Derivatives for the Introduction of Quaternary Centers. Angewandte Chemie (International Ed. in English). PMID 28467029 DOI: 10.1002/Anie.201703174 |
0.734 |
|
2016 |
Moreno J, Picazo E, Morrill LA, Smith JM, Garg NK. Enantioselective Total Syntheses of Akuammiline Alkaloids (+)-Strictamine, (-)-2(S)-Cathafoline, and (-)-Aspidophylline A. Journal of the American Chemical Society. PMID 26783944 DOI: 10.1021/Jacs.5B12880 |
0.76 |
|
2015 |
Smith JM, Moreno J, Boal BW, Garg NK. The Fischer Indolization Reaction as a Strategic Platform for the Total Synthesis of Picrinine. The Journal of Organic Chemistry. PMID 26134260 DOI: 10.1021/Acs.Joc.5B00872 |
0.765 |
|
2015 |
Smith JM, Moreno J, Boal BW, Garg NK. Cascade reactions: a driving force in akuammiline alkaloid total synthesis. Angewandte Chemie (International Ed. in English). 54: 400-12. PMID 25346244 DOI: 10.1002/Anie.201406866 |
0.754 |
|
2014 |
Smith JM, Moreno J, Boal BW, Garg NK. Total synthesis of the akuammiline alkaloid picrinine. Journal of the American Chemical Society. 136: 4504-7. PMID 24597784 DOI: 10.1021/Ja501780W |
0.737 |
|
2014 |
Smith JM, Moreno J, Boal BW, Garg NK. Kaskadenreaktionen in der Totalsynthese von Akuammilin-Alkaloiden Angewandte Chemie. 127: 410-422. DOI: 10.1002/Ange.201406866 |
0.665 |
|
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