Nathaniel Haynes Sherden - Publications

2011 Chemistry California Institute of Technology, Pasadena, CA 

9 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
2017 Sherden NH, Lichman B, Caputi L, Zhao D, Kamileen MO, Buell CR, O'Connor SE. Identification of iridoid synthases from Nepeta species: Iridoid cyclization does not determine nepetalactone stereochemistry. Phytochemistry. 145: 48-56. PMID 29091815 DOI: 10.1016/j.phytochem.2017.10.004  0.32
2015 Kries H, Caputi L, Stevenson CE, Kamileen MO, Sherden NH, Geu-Flores F, Lawson DM, O'Connor SE. Structural determinants of reductive terpene cyclization in iridoid biosynthesis. Nature Chemical Biology. PMID 26551396 DOI: 10.1038/nchembio.1955  0.84
2015 Kellner F, Geu-Flores F, Sherden NH, Brown S, Foureau E, Courdavault V, O'Connor SE. Discovery of a P450-catalyzed step in vindoline biosynthesis: a link between the aspidosperma and eburnamine alkaloids. Chemical Communications (Cambridge, England). 51: 7626-8. PMID 25850027 DOI: 10.1039/c5cc01309g  0.84
2014 Lindner S, Geu-Flores F, Bräse S, Sherden NH, O'Connor SE. Conversion of substrate analogs suggests a Michael cyclization in iridoid biosynthesis. Chemistry & Biology. 21: 1452-6. PMID 25444551 DOI: 10.1016/j.chembiol.2014.09.010  0.84
2012 Geu-Flores F, Sherden NH, Courdavault V, Burlat V, Glenn WS, Wu C, Nims E, Cui Y, O'Connor SE. An alternative route to cyclic terpenes by reductive cyclization in iridoid biosynthesis. Nature. 492: 138-42. PMID 23172143 DOI: 10.1038/nature11692  0.84
2012 Keith JA, Behenna DC, Sherden N, Mohr JT, Ma S, Marinescu SC, Nielsen RJ, Oxgaard J, Stoltz BM, Goddard WA. The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation. Journal of the American Chemical Society. 134: 19050-60. PMID 23102088 DOI: 10.1021/ja306860n  0.84
2011 Behenna DC, Mohr JT, Sherden NH, Marinescu SC, Harned AM, Tani K, Seto M, Ma S, Novák Z, Krout MR, McFadden RM, Roizen JL, Enquist JA, White DE, Levine SR, et al. Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 14199-223. PMID 22083969 DOI: 10.1002/chem.201003383  0.84
2010 Fulmer GR, Miller AJM, Sherden NH, Gottlieb HE, Nudelman A, Stoltz BM, Bercaw JE, Goldberg KI. NMR chemical shifts of trace impurities: Common laboratory solvents, organics, and gases in deuterated solvents relevant to the organometallic chemist Organometallics. 29: 2176-2179. DOI: 10.1021/om100106e  0.84
2009 Sherden NH, Behenna DC, Virgil SC, Stoltz BM. Unusual allylpalladium carboxylate complexes: identification of the resting state of catalytic enantioselective decarboxylative allylic alkylation reactions of ketones. Angewandte Chemie (International Ed. in English). 48: 6840-3. PMID 19672907 DOI: 10.1002/anie.200902575  0.84
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