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Noah Z. Burns, Ph.D. - Publications

Affiliations: 
2012- Chemistry Stanford University, Palo Alto, CA 
Area:
Organic Chemistry, Medicinal Chemistry
Website:
http://chemistry.stanford.edu/faculty/noah-burns
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33 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Derstine BC, Cook AJ, Collings JD, Gair J, Saurí J, Kwan EE, Burns NZ. Total Synthesis of (+)-Discorhabdin V. Angewandte Chemie (International Ed. in English). 63: e202315284. PMID 37956221 DOI: 10.1002/anie.202315284  0.312
2021 Patel SC, Smith MW, Mercer JAM, Suzuki K, Burns NZ. Enantioselective Cyclobutenylation of Olefins Using -Sulfonyl-1,2,3-Triazoles as Vicinal Dicarbene Equivalents. Organic Letters. PMID 34374544 DOI: 10.1021/acs.orglett.1c02331  0.363
2019 Smith MW, Falk ID, Ikemoto H, Burns NZ. A Convenient C-H Functionalization Platform for Pyrroloiminoquinone Alkaloid Synthesis. Tetrahedron. 75: 3366-3370. PMID 31889735 DOI: 10.1016/J.Tet.2019.05.009  0.38
2019 Landry ML, McKenna GM, Burns NZ. Enantioselective Synthesis of Azamerone. Journal of the American Chemical Society. PMID 30707836 DOI: 10.1021/Jacs.8B12566  0.428
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, ... ... Burns NZ, 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  0.642
2018 Seidl FJ, Min C, Lopez JA, Burns NZ. Catalytic Regio- and Enantioselective Haloazidation of Allylic Alcohols. Journal of the American Chemical Society. PMID 30403852 DOI: 10.1021/Jacs.8B10799  0.41
2018 Su JK, Feist JD, Yang J, Mercer JAM, Romaniuk JAH, Chen Z, Cegelski L, Burns NZ, Xia Y. Synthesis and Mechanochemical Activation of Ladderene-Norbornene Block Copolymers. Journal of the American Chemical Society. PMID 30229652 DOI: 10.1021/Jacs.8B08908  0.319
2018 Landry ML, Burns NZ. Catalytic Enantioselective Dihalogenation in Total Synthesis. Accounts of Chemical Research. PMID 29664281 DOI: 10.1021/Acs.Accounts.8B00064  0.509
2018 McKenna GM, Moss FR, Landry ML, Burns NZ, Boxer SG. Synthesis and Biophysical Characterization of the Chlorosulfolipids of Ochramonas danica Biophysical Journal. 114: 16a. DOI: 10.1016/J.Bpj.2017.11.129  0.41
2017 Burckle AJ, Gál B, Seidl FJ, Vasilev VH, Burns NZ. Enantiospecific Solvolytic Functionalization of Bromochlorides. Journal of the American Chemical Society. PMID 28858493 DOI: 10.1021/Jacs.7B07792  0.425
2016 Mercer JA, Cohen CM, Shuken SR, Wagner AM, Smith MW, Moss FR, Smith MD, Vahala R, Gonzalez-Martinez A, Boxer SG, Burns NZ. Chemical Synthesis and Self-Assembly of a Ladderane Phospholipid. Journal of the American Chemical Society. 138: 15845-15848. PMID 27960308 DOI: 10.1021/Jacs.6B10706  0.498
2016 Gál B, Bucher C, Burns NZ. Chiral Alkyl Halides: Underexplored Motifs in Medicine. Marine Drugs. 14. PMID 27827902 DOI: 10.3390/Md14110206  0.409
2016 Seidl FJ, Burns NZ. Selective bromochlorination of a homoallylic alcohol for the total synthesis of (-)-anverene. Beilstein Journal of Organic Chemistry. 12: 1361-5. PMID 27559385 DOI: 10.3762/Bjoc.12.129  0.338
2016 Burckle AJ, Vasilev VH, Burns NZ. A Unified Approach for the Enantioselective Synthesis of the Brominated Chamigrene Sesquiterpenes. Angewandte Chemie (International Ed. in English). PMID 27506430 DOI: 10.1002/Anie.201605722  0.423
2016 Landry ML, Hu DX, McKenna GM, Burns NZ. Catalytic Enantioselective Dihalogenation and the Selective Synthesis of (-)-Deschloromytilipin A and (-)-Danicalipin A. Journal of the American Chemical Society. PMID 27018981 DOI: 10.1021/Jacs.6B01643  0.466
2015 Mercer JA, Burns NZ. Natural products: Emulation illuminates biosynthesis. Nature Chemistry. 7: 860-1. PMID 26492003 DOI: 10.1038/Nchem.2377  0.38
2015 Bucher C, Deans RM, Burns NZ. Highly Selective Synthesis of Halomon, Plocamenone, and Isoplocamenone. Journal of the American Chemical Society. 137: 12784-7. PMID 26394844 DOI: 10.1021/Jacs.5B08398  0.496
2015 Hu DX, Seidl FJ, Bucher C, Burns NZ. Catalytic chemo-, regio-, and enantioselective bromochlorination of allylic alcohols. Journal of the American Chemical Society. 137: 3795-8. PMID 25738419 DOI: 10.1021/Jacs.5B01384  0.411
2013 Hu DX, Shibuya GM, Burns NZ. Catalytic enantioselective dibromination of allylic alcohols. Journal of the American Chemical Society. 135: 12960-3. PMID 23952929 DOI: 10.1021/Ja4083182  0.361
2013 Burns NZ, Baran PS. Point-to-Planar Chirality Transfer in Total Synthesis: Scalable and Programmable Synthesis of Haouamine A and Its Atropisomer Asymmetric Synthesis Ii: More Methods and Applications. 11-16. DOI: 10.1002/9783527652235.ch2  0.508
2012 Burns NZ, Jacobsen EN. Organic chemistry: catalysis in tight spaces. Nature. 483: 278-9. PMID 22422255 DOI: 10.1038/483278A  0.557
2011 Burns NZ, Witten MR, Jacobsen EN. Dual catalysis in enantioselective oxidopyrylium-based [5 + 2] cycloadditions. Journal of the American Chemical Society. 133: 14578-81. PMID 21848300 DOI: 10.1021/Ja206997E  0.649
2011 Burns NZ, Witten MR, Jacobsen EN. Thiourea-Catalyzed Intramolecular [5+2] Cycloadditions Synfacts. 2011: 1241-1241. DOI: 10.1055/S-0031-1289260  0.561
2010 Sella E, Weinstain R, Erez R, Burns NZ, Baran PS, Shabat D. Sulfhydryl-based dendritic chain reaction. Chemical Communications (Cambridge, England). 46: 6575-7. PMID 20714571 DOI: 10.1039/C0Cc02195D  0.478
2009 Burns NZ, Jessing M, Baran PS. Total synthesis of haouamine A: the indeno-tetrahydropyridine core. Tetrahedron. 65: 6600-6610. PMID 20161191 DOI: 10.1016/J.Tet.2009.05.075  0.552
2009 Burns NZ, Krylova IN, Hannoush RN, Baran PS. Scalable total synthesis and biological evaluation of haouamine A and its atropisomer. Journal of the American Chemical Society. 131: 9172-3. PMID 19530671 DOI: 10.1021/Ja903745S  0.593
2009 Burns NZ, Baran PS, Hoffmann RW. Redox economy in organic synthesis. Angewandte Chemie (International Ed. in English). 48: 2854-67. PMID 19294720 DOI: 10.1002/Anie.200806086  0.54
2009 Burns N, Baran P, Hoffmann R. Redoxökonomie in der organischen Synthese Angewandte Chemie. 121: 2896-2910. DOI: 10.1002/Ange.200806086  0.468
2008 Burns NZ, Baran PS. On the origin of the haouamine alkaloids. Angewandte Chemie (International Ed. in English). 47: 205-8. PMID 18038444 DOI: 10.1002/Anie.200704576  0.485
2008 Burns N, Baran P. Über den biologischen Ursprung der Haouamin-Alkaloide Angewandte Chemie. 120: 211-215. DOI: 10.1002/Ange.200704576  0.499
2006 Burns NZ, Hackman BM, Ng PY, Powelson IA, Leighton JL. The enantioselective allylation and crotylation of sterically hindered and functionalized aryl ketones: convenient access to unusual tertiary carbinol structures. Angewandte Chemie (International Ed. in English). 45: 3811-3. PMID 16671141 DOI: 10.1002/Anie.200600910  0.678
2006 Baran PS, Burns NZ. Total synthesis of (+/-)-haouamine A. Journal of the American Chemical Society. 128: 3908-9. PMID 16551088 DOI: 10.1002/CHIN.200633207  0.555
2006 Baran P, Burns N. Synthesis of (±)-Haouamine A Synfacts. 2006: 0987-0987. DOI: 10.1055/S-2006-949330  0.463
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