Noah Z. Burns, Ph.D.
Affiliations: | 2012- | Chemistry | Stanford University, Palo Alto, CA |
Area:
Organic Chemistry, Medicinal ChemistryWebsite:
http://chemistry.stanford.edu/faculty/noah-burnsGoogle:
"Noah Z. Burns"Mean distance: 7.16 | S | N | B | C | P |
Parents
Sign in to add mentor| James L. Leighton | research assistant | Columbia | ||
| Phil S. Baran | grad student | 2004-2009 | Scripps Institute | |
| (Total syntheses of haouamine A.) | ||||
| Eric N. Jacobsen | post-doc | 2012 | Harvard | |
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Publications
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| Derstine BC, Cook AJ, Collings JD, et al. (2023) Total Synthesis of (+)-Discorhabdin V. Angewandte Chemie (International Ed. in English). 63: e202315284 |
| Patel SC, Smith MW, Mercer JAM, et al. (2021) Enantioselective Cyclobutenylation of Olefins Using -Sulfonyl-1,2,3-Triazoles as Vicinal Dicarbene Equivalents. Organic Letters |
| Smith MW, Falk ID, Ikemoto H, et al. (2019) A Convenient C-H Functionalization Platform for Pyrroloiminoquinone Alkaloid Synthesis. Tetrahedron. 75: 3366-3370 |
| Landry ML, McKenna GM, Burns NZ. (2019) Enantioselective Synthesis of Azamerone. Journal of the American Chemical Society |
| Kearney SE, Zahoránszky-Kőhalmi G, Brimacombe KR, et al. (2018) Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space. Acs Central Science. 4: 1727-1741 |
| Seidl FJ, Min C, Lopez JA, et al. (2018) Catalytic Regio- and Enantioselective Haloazidation of Allylic Alcohols. Journal of the American Chemical Society |
| Su JK, Feist JD, Yang J, et al. (2018) Synthesis and Mechanochemical Activation of Ladderene-Norbornene Block Copolymers. Journal of the American Chemical Society |
| Landry ML, Burns NZ. (2018) Catalytic Enantioselective Dihalogenation in Total Synthesis. Accounts of Chemical Research |
| McKenna GM, Moss FR, Landry ML, et al. (2018) Synthesis and Biophysical Characterization of the Chlorosulfolipids of Ochramonas danica Biophysical Journal. 114: 16a |
| Burckle AJ, Gál B, Seidl FJ, et al. (2017) Enantiospecific Solvolytic Functionalization of Bromochlorides. Journal of the American Chemical Society |