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Andrew M. Harned - Publications

Affiliations: 
Chemistry University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
stereoselective synthesis of carbon-carbon and carbon-heteroatom bonds
Website:
http://www.chem.umn.edu/directory/faculty.lasso?serial=2849
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43 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
2019 Harned AM, Stoltz BM. Development of a catalytic enantioselective synthesis of the guanacastepene and heptemerone tricyclic core. Tetrahedron. 75: 3166-3177. PMID 31937979 DOI: 10.1016/J.Tet.2019.02.053  0.653
2018 Tang T, Moon NG, McKay L, Harned AM. New Strategy To Access Enantioenriched Cyclohexadienones: Kinetic Resolution of -Quinols by Organocatalytic Thiol-Michael Addition Reactions. Acs Omega. 3: 15492-15500. PMID 31458205 DOI: 10.1021/acsomega.8b01787  0.405
2018 Thorat RG, Brooks BA, Nichols B, Harned AM. Stereoselective synthesis of the C14-C23 fragment of biselyngbyolide A and B enabled by transition metal catalysis. Tetrahedron. 74: 7277-7281. PMID 30636818 DOI: 10.1016/J.Tet.2018.10.066  0.442
2018 Tang T, Harned AM. Experimental evidence for the formation of cationic intermediates during iodine(iii)-mediated oxidative dearomatization of phenols. Organic & Biomolecular Chemistry. PMID 30191933 DOI: 10.1039/C8Ob01652F  0.354
2018 Moon NG, Harned AM. Synthetic explorations of the briarane jungle: progress in developing a synthetic route to a common family of diterpenoid natural products. Royal Society Open Science. 5: 172280. PMID 29892413 DOI: 10.1098/Rsos.172280  0.339
2018 Harned AM. Concerning the mechanism of iodine(iii)-mediated oxidative dearomatization of phenols. Organic & Biomolecular Chemistry. PMID 29542797 DOI: 10.1039/C8Ob00463C  0.407
2018 Harned AM. From determination of enantiopurity to the construction of complex molecules: The Horeau principle and its application in synthesis Tetrahedron. 74: 3797-3841. DOI: 10.1016/J.Tet.2018.05.056  0.359
2017 Thorat RG, Harned AM. Rapid, enantioselective synthesis of the C1-C13 fragment of biselyngbyolide B. Chemical Communications (Cambridge, England). PMID 29199310 DOI: 10.1039/C7Cc08004B  0.328
2017 Moon NG, Harned AM. Torsional steering as friend and foe: development of a synthetic route to the briarane diterpenoid stereotetrad. Organic & Biomolecular Chemistry. PMID 28169385 DOI: 10.1039/C7Ob00124J  0.431
2015 Craig RA, Loskot SA, Mohr JT, Behenna DC, Harned AM, Stoltz BM. Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Cyclopentanones. Organic Letters. 17: 5160-3. PMID 26501770 DOI: 10.1021/Acs.Orglett.5B02376  0.805
2015 Moon NG, Harned AM. A concise synthetic route to the stereotetrad core of the briarane diterpenoids. Organic Letters. 17: 2218-21. PMID 25871809 DOI: 10.1021/Acs.Orglett.5B00816  0.429
2015 Harned AM. α-Alkylation of a norbornene-derived tricyclic ketone: are steric factors really in control? Chemical Communications (Cambridge, England). 51: 2076-9. PMID 25534696 DOI: 10.1039/C4Cc07967A  0.387
2015 Volp KA, Harned AM. Total Synthesis of Sorbicillactone A: An Inspiration for Methodology and Catalyst Development Strategies and Tactics in Organic Synthesis. 11: 253-308. DOI: 10.1016/B978-0-08-100023-6.00009-9  0.822
2014 Kalstabakken KA, Harned AM. Asymmetric transformations of achiral 2,5-cyclohexadienones. Tetrahedron. 70: 9571-9585. PMID 26688596 DOI: 10.1016/J.Tet.2014.07.081  0.827
2014 Harned AM. Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III) reagents: an opportunity for rational catalyst design? Tetrahedron Letters. 55: 4681-4689. PMID 25147412 DOI: 10.1016/J.Tetlet.2014.06.051  0.422
2014 Kalstabakken KA, Harned AM. Asymmetric transformations of achiral 2,5-cyclohexadienones Tetrahedron. 70: 9571-9585. DOI: 10.1016/j.tet.2014.07.081  0.756
2013 Volp KA, Harned AM. Origin of stereoselectivity of the alkylation of cyclohexadienone-derived bicyclic malonates. The Journal of Organic Chemistry. 78: 7554-64. PMID 23841721 DOI: 10.1021/Jo4011238  0.799
2013 Tello-Aburto R, Kalstabakken KA, Harned AM. Ligand and substrate effects during Pd-catalyzed cyclizations of alkyne-tethered cyclohexadienones. Organic & Biomolecular Chemistry. 11: 5596-604. PMID 23715063 DOI: 10.1039/C3Ob27491H  0.8
2013 Volp KA, Harned AM. Chiral aryl iodide catalysts for the enantioselective synthesis of para-quinols. Chemical Communications (Cambridge, England). 49: 3001-3. PMID 23463273 DOI: 10.1039/C3Cc00013C  0.816
2013 Kalstabakken KA, Harned AM. Spectral database for instructors: A living, online nmr fid database Journal of Chemical Education. 90: 941-943. DOI: 10.1021/Ed300787V  0.732
2013 Moon NG, Harned AM. Iodine(III)-promoted synthesis of oxazolines from N-allylamides Tetrahedron Letters. 54: 2960-2963. DOI: 10.1016/J.Tetlet.2013.03.140  0.432
2012 Bennett NB, Hong AY, Harned AM, Stoltz BM. Synthesis of enantioenriched γ-quaternary cycloheptenones using a combined allylic alkylation/Stork-Danheiser approach: preparation of mono-, bi-, and tricyclic systems. Organic & Biomolecular Chemistry. 10: 56-9. PMID 22009489 DOI: 10.1039/C1Ob06189E  0.797
2011 Hong AY, Bennett NB, Krout MR, Jensen T, Harned AM, Stoltz BM. Palladium-Catalyzed Asymmetric Alkylation in the Synthesis of Cyclopentanoid and Cycloheptanoid Core Structures Bearing All-Carbon Quaternary Stereocenters. Tetrahedron. 67: 10234-10248. PMID 22347731 DOI: 10.1016/J.Tet.2011.10.031  0.823
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  0.699
2011 Tello-Aburto R, Kalstabakken KA, Volp KA, Harned AM. Regioselective and stereoselective cyclizations of cyclohexadienones tethered to active methylene groups. Organic & Biomolecular Chemistry. 9: 7849-59. PMID 21952818 DOI: 10.1039/C1Ob06125A  0.786
2011 Harned AM, Volp KA. The sorbicillinoid family of natural products: isolation, biosynthesis, and synthetic studies. Natural Product Reports. 28: 1790-810. PMID 21927733 DOI: 10.1039/C1Np00039J  0.756
2011 Volp KA, Johnson DM, Harned AM. A concise synthetic approach to the sorbicillactones: total synthesis of sorbicillactone A and 9-epi-sorbicillactone A. Organic Letters. 13: 4486-9. PMID 21797286 DOI: 10.1021/Ol201211F  0.813
2011 Hong AY, Krout MR, Jensen T, Bennett NB, Harned AM, Stoltz BM. Ring-contraction strategy for the practical, scalable, catalytic asymmetric synthesis of versatile γ-quaternary acylcyclopentenes. Angewandte Chemie (International Ed. in English). 50: 2756-60. PMID 21387482 DOI: 10.1002/Anie.201007814  0.84
2011 Lang PT, Harned AM, Wissinger JE. Oxidation of borneol to camphor using oxone and catalytic sodium chloride: A green experiment for the undergraduate organic chemistry laboratory Journal of Chemical Education. 88: 652-656. DOI: 10.1021/Ed100853F  0.381
2010 Harned AM, Hanson PR. ChemInform Abstract: Capture-ROMP-Release: Application for the Synthesis of O-Alkylhydroxylamines. Cheminform. 33: no-no. DOI: 10.1002/chin.200235081  0.449
2009 Rout L, Harned AM. Allene carboxylates as dipolarophiles in rh-catalyzed carbonyl ylide cycloadditions. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 12926-8. PMID 19894232 DOI: 10.1002/Chem.200902208  0.804
2009 Tello-Aburto R, Harned AM. Palladium-catalyzed reactions of cyclohexadienones: regioselective cyclizations triggered by alkyne acetoxylation. Organic Letters. 11: 3998-4000. PMID 19708708 DOI: 10.1021/Ol901642W  0.512
2005 Mohr JT, Behenna DC, Harned AM, Stoltz BM. Deracemization of quaternary stereocenters by Pd-catalyzed enantioconvergent decarboxylative allylation of racemic beta-ketoesters. Angewandte Chemie (International Ed. in English). 44: 6924-7. PMID 16206310 DOI: 10.1002/Anie.200502018  0.797
2005 Harned AM, He HS, Toy PH, Flynn DL, Hanson PR. Multipolymer solution-phase reactions: application to the Mitsunobu reaction. Journal of the American Chemical Society. 127: 52-3. PMID 15631444 DOI: 10.1021/Ja045188R  0.574
2005 Stoltz B, Mohr J, Behenna D, Harned A. Quaternary Carbon Center Formation by Decarboxylation of Allyl β-Ketoesters Synfacts. 2006: 0053-0053. DOI: 10.1055/S-2005-921674  0.769
2005 Harned AM, Sherrill WM, Flynn DL, Hanson PR. High-load, soluble oligomeric benzenesulfonyl azide: Application to facile diazo-transfer reactions Tetrahedron. 61: 12093-12099. DOI: 10.1016/J.Tet.2005.08.120  0.565
2005 Harned AM, Zhang M, Vedantham P, Mukherjee S, Herpel RH, Flynn DL, Hanson PR. ROM polymerization in facilitated synthesis Aldrichimica Acta. 38: 4-17.  0.574
2003 Harned AM, Mukherjee S, Flynn DL, Hanson PR. Ring-opening metathesis phase-trafficking (ROMpt) synthesis: multistep synthesis on soluble ROM supports. Organic Letters. 5: 15-8. PMID 12509879 DOI: 10.1021/Ol0270327  0.612
2002 Moore JD, Harned AM, Henle J, Flynn DL, Hanson PR. Scavenge-ROMP-filter: a facile strategy for soluble scavenging via norbornenyl tagging of electrophilic Reagents. Organic Letters. 4: 1847-9. PMID 12027629 DOI: 10.1021/Ol0257880  0.634
2002 Harned AM, Hanson PR. Capture-ROMP-release: application for the synthesis of O-alkylhydroxylamines. Organic Letters. 4: 1007-10. PMID 11893208 DOI: 10.1021/Ol025577V  0.507
2002 Wanner J, Sprott KT, Poon K, Harned A, Probst D, Sheriff B, Petz M, Hanson PR. Ring-opening metathesis polymerization approach to phosphorus-containing biooligomers Phosphorus, Sulfur and Silicon and Related Elements. 177: 1971-1972. DOI: 10.1080/10426500213332  0.76
2002 Wanner J, Harned AM, Probst DA, Poon KWC, Klein TA, Snelgrove KA, Hanson PR. A dual metathesis route to oligomeric sulfonamides Tetrahedron Letters. 43: 917-921. DOI: 10.1016/S0040-4039(01)02293-6  0.826
2002 Harned AM, Hanson PR, Flynn DL. Natural product synthesis utilizing solid-supported reagents Chemtracts. 15: 630-636.  0.538
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