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Daniel Seidel, Ph.D. - Publications

Affiliations: 
2005-2017 Rutgers University, New Brunswick, New Brunswick, NJ, United States 
 2017- University of Florida, Gainesville, Gainesville, FL, United States 
Area:
Organic Chemistry
Website:
http://www.seidel-group.com/2.html
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53 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
2014 Mittal N, Sun DX, Seidel D. Conjugate-base-stabilized Brønsted acids: catalytic enantioselective Pictet-Spengler reactions with unmodified tryptamine. Organic Letters. 16: 1012-5. PMID 24446703 DOI: 10.1021/Ol403773A  0.343
2013 Richers MT, Deb I, Platonova AY, Zhang C, Seidel D. Facile Access to Ring-Fused Aminals via Direct α-Amination of Secondary Amines with ortho-Aminobenzaldehydes. Synthesis of Vasicine, Deoxyvasicine, Deoxyvasicinone, Mackinazolinone and Ruteacarpine. Synthesis. 45: 1430-1748. PMID 24052668  0.672
2013 Richers MT, Deb I, Platonova AY, Zhang C, Seidel D. Facile access to ring-fused aminals via direct α-amination of secondary amines with o-aminobenzaldehydes: Synthesis of vasicine, deoxyvasicine, deoxyvasicinone, mackinazolinone, and ruteacarpine Synthesis (Germany). 45: 1730-1748. DOI: 10.1055/S-0033-1338852  0.669
2012 Mittal N, Sun DX, Seidel D. Kinetic resolution of amines via dual catalysis: remarkable dependence of selectivity on the achiral cocatalyst. Organic Letters. 14: 3084-7. PMID 22650801 DOI: 10.1021/Ol301155B  0.338
2011 Das D, Richers MT, Ma L, Seidel D. The decarboxylative Strecker reaction. Organic Letters. 13: 6584-7. PMID 22087753 DOI: 10.1021/Ol202957D  0.353
2011 De CK, Seidel D. Catalytic enantioselective desymmetrization of meso-diamines: a dual small-molecule catalysis approach. Journal of the American Chemical Society. 133: 14538-41. PMID 21863902 DOI: 10.1021/Ja2060462  0.32
2011 Deb I, Coiro DJ, Seidel D. Decarboxylative formation of N-alkyl pyrroles from 4-hydroxyproline. Chemical Communications (Cambridge, England). 47: 6473-5. PMID 21556391 DOI: 10.1039/C1Cc11560J  0.64
2011 Klauber EG, Mittal N, Shah TK, Seidel D. A dual-catalysis/anion-binding approach to the kinetic resolution of allylic amines. Organic Letters. 13: 2464-7. PMID 21476518 DOI: 10.1021/ol200712b  0.489
2011 Haibach MC, Deb I, De CK, Seidel D. Redox-neutral indole annulation cascades. Journal of the American Chemical Society. 133: 2100-3. PMID 21280625 DOI: 10.1021/Ja110713K  0.672
2011 Deb I, Das D, Seidel D. Redox isomerization via azomethine ylide intermediates: N-alkyl indoles from indolines and aldehydes. Organic Letters. 13: 812-5. PMID 21247142 DOI: 10.1021/Ol1031359  0.676
2010 Li L, Seidel D. Catalytic enantioselective Friedländer condensations: facile access to quinolines with remote stereogenic centers. Organic Letters. 12: 5064-7. PMID 20936865 DOI: 10.1021/Ol1023932  0.397
2010 Klauber EG, De CK, Shah TK, Seidel D. Merging nucleophilic and hydrogen bonding catalysis: an anion binding approach to the kinetic resolution of propargylic amines. Journal of the American Chemical Society. 132: 13624-6. PMID 20843041 DOI: 10.1021/ja105337h  0.469
2010 Zhang C, Seidel D. Nontraditional reactions of azomethine ylides: decarboxylative three-component couplings of alpha-amino acids. Journal of the American Chemical Society. 132: 1798-9. PMID 20104842 DOI: 10.1021/Ja910719X  0.352
2010 Seidel D, Klauber E, De C, Shah T. Asymmetric Anion Binding DMAP Catalysis in the Kinetic Resolution of Propargylic Amines Synfacts. 2010: 1426-1426. DOI: 10.1055/s-0030-1258920  0.452
2010 Seidel D. Cinchona Alkaloids in Synthesis & Catalysis: Ligands, Immobilization and Organocatalysis Cinchona Alkaloids in Synthesis & Catalysis: Ligands, Immobilization and Organocatalysis . Edited by Choong Eui Song (Sungkyunkwan University, Suwon, Republik Korea). WILEY-VCH Verlag GmbH & Co. KGaA: Weinheim. 2009. 526 pp. $129.95. ISBN 978-3-527-32416-3 . Journal of the American Chemical Society. 132: 8224-8224. DOI: 10.1021/Ja103586V  0.337
2010 Deb I, Seidel D. Retro-Claisen condensation versus pyrrole formation in reactions of amines and 1,3-diketones Tetrahedron Letters. 51: 2945-2947. DOI: 10.1016/J.Tetlet.2010.03.086  0.665
2009 De CK, Klauber EG, Seidel D. Merging nucleophilic and hydrogen bonding catalysis: an anion binding approach to the kinetic resolution of amines. Journal of the American Chemical Society. 131: 17060-1. PMID 19929016 DOI: 10.1021/Ja9079435  0.335
2009 Murarka S, Deb I, Zhang C, Seidel D. Catalytic enantioselective intramolecular redox reactions: ring-fused tetrahydroquinolines. Journal of the American Chemical Society. 131: 13226-7. PMID 19711900 DOI: 10.1021/Ja905213F  0.676
2009 Li L, Ganesh M, Seidel D. Catalytic enantioselective synthesis of alpha,beta-diamino acid derivatives. Journal of the American Chemical Society. 131: 11648-9. PMID 19642698 DOI: 10.1021/Ja9034494  0.304
2009 Zhang C, Murarka S, Seidel D. Facile formation of cyclic aminals through a Brønsted acid-promoted redox process. The Journal of Organic Chemistry. 74: 419-22. PMID 19053590 DOI: 10.1021/Jo802325X  0.346
2009 Seidel D, Murarka S, Deb I, Zhang C. Catalytic Enantioselective Synthesis of Ring-Fused Tetrahydroquinolines Synfacts. 2009: 1352-1352. DOI: 10.1055/s-0029-1218321  0.653
2008 Zhang C, De CK, Mal R, Seidel D. Alpha-amination of nitrogen heterocycles: ring-fused aminals. Journal of the American Chemical Society. 130: 416-7. PMID 18081292 DOI: 10.1021/Ja077473R  0.359
2007 Evans DA, Mito S, Seidel D. Scope and mechanism of enantioselective Michael additions of 1,3-dicarbonyl compounds to nitroalkenes catalyzed by nickel(II)-diamine complexes. Journal of the American Chemical Society. 129: 11583-92. PMID 17718492 DOI: 10.1021/Ja0735913  0.417
2007 Melfi PJ, Kim SK, Lee JT, Bolze F, Seidel D, Lynch VM, Veauthier JM, Gaunt AJ, Neu MP, Ou Z, Kadish KM, Fukuzumi S, Ohkubo K, Sessler JL. Redox behavior of cyclo[6]pyrrole in the formation of a uranyl complex. Inorganic Chemistry. 46: 5143-5. PMID 17511451 DOI: 10.1021/Ic700781T  0.731
2006 Yoon ZS, Kwon JH, Yoon MC, Koh MK, Noh SB, Sessler JL, Lee JT, Seidel D, Aguilar A, Shimizu S, Suzuki M, Osuka A, Kim D. Nonlinear optical properties and excited-state dynamics of highly symmetric expanded porphyrins. Journal of the American Chemical Society. 128: 14128-34. PMID 17061896 DOI: 10.1021/Ja064773K  0.566
2005 Evans DA, Seidel D. Ni(II)-Bis[(R,R)-N,N'-dibenzylcyclohexane-1,2-diamine]Br2 catalyzed enantioselective Michael additions of 1,3-dicarbonyl compounds to conjugated nitroalkenes. Journal of the American Chemical Society. 127: 9958-9. PMID 16011333 DOI: 10.1021/Ja052935R  0.429
2005 Sessler JL, Aguilar A, Sanchez-Garcia D, Seidel D, Köhler T, Arp F, Lynch VM. Facile syntheses of quater-, penta-, and sexipyrroles. Organic Letters. 7: 1887-90. PMID 15876011 DOI: 10.1021/Ol050151C  0.726
2005 Gorski A, Köhler T, Seidel D, Lee JT, Orzanowska G, Sessler JL, Waluk J. Electronic structure, spectra, and magnetic circular dichroism of cyclohexa-, cyclohepta-, and cyclooctapyrrole. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 4179-84. PMID 15861478 DOI: 10.1002/Chem.200401343  0.546
2005 Sanchez-Garcia D, Kohler T, Seidel D, Lynch V, Sessler JL. Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles. Chemical Communications (Cambridge, England). 2122-4. PMID 15846420 DOI: 10.1039/B500735F  0.721
2004 Köhler T, Ou Z, Lee JT, Seidel D, Lynch V, Kadish KM, Sessler JL. Reductive N alkylation of cyclo[8]pyrroles. Angewandte Chemie (International Ed. in English). 44: 83-7. PMID 15599897 DOI: 10.1002/Anie.200461801  0.574
2004 Köhler T, Hodgson MC, Seidel D, Veauthier JM, Meyer S, Lynch V, Boyd PD, Brothers PJ, Sessler JL. Octaethylporphyrin and expanded porphyrin complexes containing coordinated BF2 groups. Chemical Communications (Cambridge, England). 1060-1. PMID 15116184 DOI: 10.1039/B400596A  0.507
2004 Sessler JL, Melfi PJ, Seidel D, Gorden AEV, Ford DK, Palmer PD, Tait CD. Hexaphyrin(1.0.1.0.0.0). A new colorimetric actinide sensor Tetrahedron. 60: 11089-11097. DOI: 10.1016/J.Tet.2004.08.055  0.739
2003 Sessler JL, Seidel D. Synthetic expanded porphyrin chemistry. Angewandte Chemie (International Ed. in English). 42: 5134-75. PMID 14601164 DOI: 10.1002/Anie.200200561  0.379
2003 Evans DA, Seidel D, Rueping M, Lam HW, Shaw JT, Downey CW. A new copper acetate-bis(oxazoline)-catalyzed, enantioselective Henry reaction. Journal of the American Chemical Society. 125: 12692-3. PMID 14558801 DOI: 10.1021/Ja0373871  0.743
2003 Köhler T, Seidel D, Lynch V, Arp FO, Ou Z, Kadish KM, Sessler JL. Formation and properties of cyclo[6]pyrrole and cyclo[7]pyrrole. Journal of the American Chemical Society. 125: 6872-3. PMID 12783532 DOI: 10.1021/Ja035089Y  0.446
2003 Sessler JL, Seidel D. Synthesechemie expandierter Porphyrine Angewandte Chemie. 115: 5292-5333. DOI: 10.1002/Ange.200200561  0.419
2002 Seidel D, Lynch V, Sessler JL. Cyclo[8]pyrrole: a simple-to-make expanded porphyrin with no meso bridges. Angewandte Chemie (International Ed. in English). 41: 1422-5. PMID 19750786 DOI: 10.1002/1521-3773(20020415)41:8<1422::Aid-Anie1422>3.0.Co;2-O  0.48
2002 Bucher C, Seidel D, Lynch V, Sessler JL. [30]heptaphyrin(1.1.1.1.1.0.0): an aromatic expanded porphyrin with a 'figure eight' like structure. Chemical Communications (Cambridge, England). 328-9. PMID 12120058 DOI: 10.1039/B109877B  0.347
2002 Sessler JL, Gorden AEV, Seidel D, Hannah S, Lynch V, Gordon PL, Donohoe RJ, Tait CD, Keogh DW. Characterization of the interactions between neptunyl and plutonyl cations and expanded porphyrins Inorganica Chimica Acta. 341: 54-70. DOI: 10.1016/S0020-1693(02)01202-1  0.502
2002 Seidel D, Lynch V, Sessler JL. Cover Picture: Angew. Chem. Int. Ed. 8/2002 Angewandte Chemie International Edition. 41: 1255-1255. DOI: 10.1002/1521-3773(20020415)41:8<1255::Aid-Anie1255>3.0.Co;2-C  0.483
2002 Seidel D, Lynch V, Sessler JL. Cyclo[8]pyrrole: A Simple-to-Make Expanded Porphyrin with No Meso Bridges This work was supported by the National Science Foundation (grant CHE 0107732 to J.L.S.). The authors would like to thank Dr. Paul Fleitz and Weijie Su (Wright Patterson Air Force Base) for recording the UV/Vis spectrum of 2 b. Angewandte Chemie. 114: 1480. DOI: 10.1002/1521-3757(20020415)114:8<1480::Aid-Ange1480>3.0.Co;2-8  0.395
2002 Seidel D, Lynch V, Sessler JL. Titelbild: Angew. Chem. 8/2002 Angewandte Chemie. 114: 1305. DOI: 10.1002/1521-3757(20020415)114:8<1305::Aid-Ange1305>3.0.Co;2-0  0.364
2001 Sessler JL, Seidel D, Vivian AE, Lynch V, Scott BL, Keogh DW. Hexaphyrin(1.0.1.0.0.0): An Expanded Porphyrin Ligand for the Actinide Cations Uranyl (UO ) and Neptunyl (NpO ). Angewandte Chemie (International Ed. in English). 40: 591-594. PMID 29712023 DOI: 10.1002/1521-3773(20010202)40:3<591::Aid-Anie591>3.0.Co;2-0  0.453
2001 Sessler JL, Seidel D, Bucher C, Lynch V. Novel, terpyrrole-containing, aromatic expanded porphyrins Tetrahedron. 57: 3743-3752. DOI: 10.1016/S0040-4020(01)00243-5  0.482
2001 Hannah S, Seidel D, Sessler JL, Lynch V. New chemistry of amethyrin Inorganica Chimica Acta. 317: 211-217. DOI: 10.1016/S0020-1693(01)00363-2  0.504
2001 Sessler J, Vivian A, Seidel D, Burrell A, Hoehner M, Mody T, Gebauer A, Weghorn S, Lynch V. Erratum to “Actinide expanded porphyrin complexes” Coordination Chemistry Reviews. 222: 275. DOI: 10.1016/S0010-8545(01)00430-1  0.592
2001 Sessler JL, Vivian AE, Seidel D, Burrell AK, Hoehner M, Mody TD, Gebauer A, Weghorn SJ, Lynch V. Actinide expanded porphyrin complexes Coordination Chemistry Reviews. 216: 411-434. DOI: 10.1016/S0010-8545(00)00395-7  0.621
2000 Keutel H, Seidel D, Klussmann M, Görls H. An unusual metal-mediated formation of an asymmetrical carboxylate-bridged dinuclear copper(II) complex Inorganic Chemistry. 39: 1608-1610. PMID 12526474 DOI: 10.1021/Ic990374X  0.333
2000 Bucher C, Seidel D, Lynch V, Kral V, Sessler JL. Novel synthesis of hybrid calixphyrin macrocycles Organic Letters. 2: 3103-6. PMID 11009356 DOI: 10.1021/Ol006316T  0.491
2000 Král V, Sessler JL, Zimmerman RS, Seidel D, Lynch V, Andrioletti B. Calixphyrins: Novel Macrocycles at the Intersection between Porphyrins and Calixpyrroles This work was supported by the National Institutes of Health (CA-68682, GM-58907, and TW-00682 to J.L.S.), the National Science Foundation (CHE-9725399 to J.L.S. and CHE-9807702 to V.L. for the purchase of the Nonius Kappa CCD), the Howard Hughes Foundation (V.K. and J.L.S.), the Grant Agency of the Czech Republic (No. 203/97/1099 to V.K.), the Ministry of Education (No. VS-97135 and Project CEZ: J19/98: 223400008 to V.K.), and the Howard Hughes Medical Institute (74195-541101 to V.K.). Angewandte Chemie (International Ed. in English). 39: 1055-1058. PMID 10760920 DOI: 10.1002/(Sici)1521-3773(20000317)39:6<1055::Aid-Anie1055>3.0.Co;2-O  0.549
1999 Sessler JL, Tvermoes NA, Davis J, Anzenbacher P, Jursíková K, Sato W, Seidel D, Lynch V, Black CB, Try A, Andrioletti B, Hemmi G, Mody TD, Magda DJ, Král V. Expanded porphyrins. Synthetic materials with potential medical utility Pure and Applied Chemistry. 71: 2009-2018. DOI: 10.1351/Pac199971112009  0.737
1999 Sessler JL, Seidel D, Lynch V. Synthesis of [28]heptaphyrin(1.0.0.1.0.0.0) and [32]Octaphyrin(1.0.0.0.1.0.0.0) via a directed oxidative ring closure: The first expanded porphyrins containing a quaterpyrrole subunit [18] Journal of the American Chemical Society. 121: 11257-11258. DOI: 10.1021/Ja992934X  0.47
1999 Sessler JL, Tvermoes NA, Davis J, Anzenbacher P, Jursíková K, Sato W, Seidel D, Lynch V, Black CB, Try A, Andrioletti B, Hemmi G, Mody TD, Magda DJ, Král V. Expanded porphyrins. Synthetic materials with potential medical utility Pure and Applied Chemistry. 71: 2009-2018.  0.726
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