<\/p>\n\n\n\n
50. \u201cCreating a culture of green chemistry and innovation in the organic laboratory<\/a>,\u201d D.A.\u00a0Vosburg,\u00a0Sustainability & Circularity NOW<\/em>\u00a02026<\/strong>,\u00a03<\/em>, a28148200. 48. \u201cAlternatives to dichloromethane for teaching laboratories<\/a>,\u201d A. Milo, L. Chen, K.A. Grice, D.A. Vosburg, J. Chem. Educ.<\/em> 2025<\/strong>, 102<\/em>, 2261-2267.<\/p>\n\n\n\n 47. \u201cOne-pot synthesis and biological evaluation of N<\/em>-fused imidazoles as antibacterial agents and bacterial topoisomerase inhibitors<\/a>,\u201d E.P. Bentley, O.W. Song, I. Glassman, L. Johar, C.A. Alcantara, V.L. Show, A.R. Johnson, H. Szurmant, D.A. Vosburg, Res. Chem.<\/em> 2025<\/strong>, 15<\/em>, 102191.<\/p>\n\n\n\n 46. \u201cTCFH\u2013NMI ketone synthesis inspired by nucleophilicity scales<\/a>,\u201d J.H. Ho, G.H. Miller, K.K. Chung, S.D. Neibert, G.L. Beutner, D.A. Vosburg, Org. Lett.<\/em> 2024<\/strong>, 26<\/em>, 8904-8909.<\/p>\n\n\n\n 45. \u201cBeyond amide bond formation: TCFH as a reagent for esterification<\/a>,\u201d N.R. Luis, K.K. Chung, M.R. Hickey, Z. Lin, G.L. Beutner, D.A. Vosburg, Org. Lett.<\/em> 2024<\/strong>, 26<\/em>, 2745-2750.<\/p>\n\n\n\n 44. \u201cFacile amide bond formation with TCFH\u2013NMI in an organic laboratory course<\/a>,\u201d O.W.M. Baldwin, L.H. Conrad-Marut, G.L. Beutner, D.A. Vosburg, J. Chem. Educ.<\/em>, 2022<\/strong>, 99<\/em>, 3747-3751.<\/p>\n\n\n\n 43. \u201cMulticomponent synthesis of lidocaine at room temperature<\/a>,\u201d M. Lee, N.J. Vosburg, E.A. Shimizu, M.A. Renter\u00eda-G\u00f3mez, R. G\u00e1mez-Monta\u00f1o, D.A. Vosburg, J. Chem. Educ.<\/em>,<\/strong> 2022<\/strong>, 99<\/i>, 2399-2402.<\/p>\n\n\n\n 42. “Disorientation, adaptation, empathy, and grace<\/a>,” D.A. Vosburg, J. Res. Pract. Coll. Teach., <\/em>2021,<\/strong> 6.<\/p>\n\n\n\n 41. \u201cEngaging undergraduates in sustainability education and research<\/a>,\u201d D.A. Vosburg, InChemistry Education for a Sustainable Society. Vol 2: Innovations in Undergraduate Curricula<\/em>, ed. S.O. Obare, C.H. Middlecamp, K.E. Peterman, Washington, DC: American Chemical Society, 2020<\/strong>, pp. 63-73.<\/p>\n\n\n\n 40. \u201cAnthraquinones: Versatile organic photocatalysts<\/a>,\u201d J. Cervantes-Gonz\u00e1lez, D.A. Vosburg, S.E. Mora-Rodriguez, M.A. V\u00e1zquez, L.G. Zepeda, C. Villegas G\u00f3mez, S. Lagunas Rivera, ChemCatChem, <\/em>2020<\/strong>, 12<\/i>, 3811-3827.<\/p>\n\n\n\n 39. \u201cHow do I design a chemical reaction to do useful work?<\/a> Reinvigorating general chemistry by connecting chemistry and society,\u201d K.M. Van Heuvelen, G.W. Daub, L.N. Hawkins, A.R. Johnson, H. Van Ryswyk, D.A. Vosburg, J. Chem. Educ.,<\/em> <\/strong>2020<\/strong>, 97<\/i>, 925-933. <\/p>\n\n\n\n 38. \u201cEmphasizing learning: The impact of student surveys in the reform of an introductory chemistry course<\/a>,\u201d K.M. Van Heuvelen, L.P. Blake, L.P., G.W. Daub, L.N. Hawkins, A.R. Johnson, H. Van Ryswyk, D.A. Vosburg, Journal of Assessment and Institutional Effectiveness,<\/em> <\/strong>2019<\/strong>,9<\/i>, 1-28.<\/p>\n\n\n\n 37. \u201cSynthesis of tris-heterocycles via a cascade IMCR\/aza Diels\u2013Alder + CuAAC strategy<\/a>,\u201d M.A. Renter\u00eda-G\u00f3mez, A., Islas-J\u00e1come, S.G. Pharande, D.A. Vosburg, R. G\u00e1mez-Monta\u00f1o, Front. Chem.,<\/em> <\/strong>2019<\/strong>, 7<\/i>, 546.<\/p>\n\n\n\n 36. \u201cAqueous dearomatization\/Diels\u2013Alder cascade to a grandifloracin precursor<\/a>,\u201d E.A. Shimizu, B. Cory, J. Hoang, G.G. Castro, M.E. Jung, D.A. Vosburg, J. Chem. Educ.,<\/em> <\/strong>2019<\/strong>, 96<\/em>, 998-1001.<\/p>\n\n\n\n 35. \u201cCanvass: A crowd-sourced, natural-product screening library for exploring biological space<\/a>,\u201d S.E. Kearney, G. Zahor\u00e1nszky-K\u0151halmi, K.R. Brimacombe, M.J. Henderson, C. Lynch, T. Zhao, K.K. Wan, Z. Itkin, C. Dillon, M. Shen, D.M. Cheff, T.D. Lee, D. Bougie, K. Cheng, N.P. Coussens, D. Dorjsuren, R.T. Eastman, R. Huang, M.J. Iannotti, S. Karavadhi, C. Klumpp-Thomas, J.S. Roth, S. Sakamuru, W. Sun, S.A. Titus, A. Yasgar, Y.Q. Zhang, J. Zhao, R.B. Andrade, M.K. Brown, N.Z Burns, J.K. Cha, E.E. Mevers, J. Clardy, J.A. Clement, P.A. Crooks, G.D. Cuny, J. Ganor, J. Moreno, L.A. Morrill, E. Picazo, R.B. Susick, N.K. Garg, B.C. Goess, R.B. Crossman, C.C. Hughes, J.N. Johnston, M.M. Joullie, A.D. Kinghorn, D.G.I. Kingston, M.J. Krische, O. Kwon, T.J. Maimone, S. Majumdar, K.M. Maloney, E. Mohamed, B.T. Murphy, P. Nagorny, D.E. Olson, L.E. Overman, L.E. Brown, J.K. Snyder, J.A. Porco, F. Rivas, Jr., S.A. Ross, R. Sarpong, I. Sharma, J.T. Shaw, Z. Xu, B. Shen, W. Shi, C.R.J. Stephenson, A.L. Verano, D.S. Tan, Y. Tang, R.E. Taylor, R.J. Thomson, D.A. Vosburg, J. Wu, W.M. Wuest, A. Zakarian, Y. Zhang, T. Ren, Z. Zuo, J. Inglese, S. Michael, A. Simeonov, W. Zheng, P. Shinn, A. Jadhav, M.B. Boxer, M.D. Hall, M. Xia, R. Guha, J.M. Rohde, ACS Cent., Sci<\/em>., 2018<\/strong>, 4<\/em>, 1727-1741.<\/p>\n\n\n\n 34. \u201cDivergent Diels-Alder reactions in the biosynthesis and synthesis of endiandric-type tetracycles: A computational study<\/a>,\u201d K.J. Kron, M. Kosich, R.J. Cave, D.A. Vosburg, J. Org. Chem<\/em>., 2018<\/strong>, 83<\/em>, 10941-10947.<\/p>\n\n\n\n 33. \u201cConcise, diastereoconvergent synthesis of endiandric-type tetracycles by iterative cross coupling<\/a>,\u201d E.B. Go, S.P. Wetzler, L.J. Kim, A.Y. Chang, D.A. Vosburg, Tetrahedron,<\/em> <\/strong>2016<\/strong>, 72<\/em>, 3790-3794.<\/p>\n\n\n\n 32.\u201cSelf-assembly, guest capture, and NMR spectroscopy of a metal\u2013organic cage in water<\/a>,\u201d E.B. Go, V. Srisuknimit, S.L. Cheng, D.A. Vosburg, J<\/em>. Chem. Educ.,<\/em> <\/strong>2016<\/strong>, 93<\/em>, 368-371. Featured on the journal cover.<\/a><\/p>\n\n\n\n 31. \u201cDirect, biomimetic synthesis of (+)-artemone via a stereoselective, organocatalytic cyclization<\/a>,\u201d E.D. Nacsa, B.C. Fielder, S.P. Wetzler, V. Srisuknimit, J.P. Litz, M.J. Van Vleet, K. Quach, D.A. Vosburg, Synthesis,<\/em> <\/strong>2015<\/strong>, 47<\/em>, 2599-2602. Featured in Organic Chemistry Highlights<\/a> and in “Navigating the chiral pool in the total synthesis of complex terpene natural products<\/a>,” Brill, Z.G., Condakes, M.L., Ting, C.P., Maimone, T.J., Chem. Rev<\/em>., 2017<\/strong>, 117<\/em>, 11753-11795).<\/p>\n\n\n\n 30.\u201cRadicinin fromCochliobolus<\/em>sp. inhibitsXylella fastidiosa<\/em>, the causal agent of Pierce\u2019s Disease of grapevine<\/a>,\u201d T.J. Aldrich, P.E. Rolshausen, M.C. Roper, J.M. Reader, M.J. Steinhaus, J. Rapicavoli, D.A. Vosburg, K.N. Maloney, Phytochemistry, <\/em>2015<\/strong>, 116<\/em>, 130-137, DOI: 10.1016\/j.phytochem.2015.03.015.<\/p>\n\n\n\n 29. \u201cCooperative loading and release behavior of a metal-organic receptor<\/a>,\u201d Q. Gan. T.K. Ronson, D.A. Vosburg, J.D. Thoburn, J.R. Nitschke, J. Am. Chem. Soc., <\/em>2015<\/strong>, 137<\/em>, 1770-1773.<\/p>\n\n\n\n 28. \u201c\u2018Solvent-free synthesis and fluorescence of a thiol-reactive sensor for undergraduate organic laboratories<\/a>,\u201d A.L. Patterson, M.D. May, B.J. Visser, A.A. Kislukhin, D.A. Vosburg, J<\/em>. Chem. Educ.,<\/em> <\/strong>2013<\/strong>, 90<\/em>, 1685-1687.<\/p>\n\n\n\n 27. \u201c\u2018Click\u2019 and olefin metathesis chemistry in water at room temperature enabled by biodegradable micelles<\/a>,\u201d B.H. Lipshutz, Z. Boskovic, C.S. Crowe, V.K. Davis, H.C. Whittemore, D.A. Vosburg, A.G. Wenzel, J. Chem. Educ<\/em>., 2013<\/strong>, 90<\/em>, 1514-1517.<\/p>\n\n\n\n 26.\u201cSynthesis ofcis<\/em>andtrans<\/em>davanoids: Artemone, hydroxydavanone, isodavanone, and nordavanone<\/a>,\u201d K.K. Wan, C.D. Evans-Klock, B.C. Fielder, D.A. Vosburg, Synthesis,<\/em> 2013<\/strong>,45<\/em>, 1541-1545.<\/p>\n\n\n\n 25. \u201cGreen chemistry and biochemistry,\u201d Vosburg, D.A., In Chemistry for Changing Times<\/em>, J.W. Hill, T.W. McCreary, D.K. Kolb, 13th edition. New York: Pearson, 2012<\/strong>, p. 467.<\/p>\n\n\n\n 24. \u201cChemoselective reactions of citral: Green syntheses of natural perfumes<\/a>,\u201d A.D. Cunningham, E.Y. Ham, D.A. Vosburg, J. Chem. Educ<\/em>., 2011<\/strong>,88<\/em>, 322-324.<\/p>\n\n\n\n 23. \u201cTwo-step, stereoselective synthesis of linalyl oxides by asymmetric allylicO<\/em>-alkylation<\/a>,\u201d K.K. Wan, J.P. Litz, D.A. Vosburg, Tetrahedron Asymm<\/em>., 2010<\/strong>,21<\/em>, 2425-2428.<\/p>\n\n\n\n 22. \u201cGreen, enzymatic syntheses of divanillin and diapocynin for the organic, biochemistry, or advanced general chemistry laboratory<\/a>,\u201d R.T. Nishimura, C.H. Giammanco, D.A. Vosburg, J. Chem. Educ<\/em>., 2010<\/strong>,87<\/em>, 526-527.<\/p>\n\n\n\n 21. \u201cA green, enantioselective synthesis of warfarin for the undergraduate organic laboratory<\/a>,\u201d T.C. Wong, C.M. Sultana, D.A. Vosburg, J. Chem. Educ<\/em>., 2010<\/strong>,87<\/em>, 194-195.<\/p>\n\n\n\n 20. \u201cA concise, biomimetic total synthesis of (+)-davanone<\/a>,\u201d K.C. Morrison, J.P. Litz, K.P. Scherpelz, D.P. Dossa, D.A. Vosburg, Org. Lett<\/em>., 2009<\/strong>,11<\/em>, 2217-2218, (highlighted in \u201cThe economies of synthesis<\/a>,\u201d T. Newhouse, P.S. Baran, R.W. Hoffmann, Chem. Soc. Rev<\/em>., 2009<\/strong>, 38<\/em>, 3010-3021).<\/p>\n\n\n\n 19. \u201cTeaching organic synthesis: a comparative case study approach<\/a>,\u201d D.A. Vosburg, J. Chem. Educ<\/em>., 2008<\/strong>, 85<\/em>, 1519-1523. Highlighted in “Novel organic courses<\/a>,” A.W. Clauss, on page 1523 of same issue.<\/p>\n\n\n\n 18. “Dynamic thiolation-thioesterase structure of a non-ribosomal peptide synthetase,” D.P. Frueh, H. Arthanari, A. Koglin, D.A. Vosburg, A.E. Bennett, C.T. Walsh, G. Wagner, N<\/em>ature,<\/em> <\/strong>2008<\/strong>, 454<\/em>, 903-906 (highlighted on pages 832-833 of same issue).<\/p>\n\n\n\n 17. “Characterization of the aminocarboxycyclopropane-forming enzyme CmaC,” W.L. Kelly, M.T. Boyne, II, E. Yeh, D.A. Vosburg, D.P. Galonic, N.L. Kelleher, C.T. Walsh, Biochemistry,<\/em> <\/strong>2007<\/strong>, 46<\/em>, 359-368.<\/p>\n\n\n\n 16. “Enzymatic generation of the antimetabolite \u03b3,\u03b3-dichloroaminobutyrate by NRPS and mononuclear iron halogenase action in a streptomycete,” M. Ueki, D.P. Galonic, F.H. Vaillancourt, S. Garneau-Tsodikova, E. Yeh, D.A. Vosburg, F.C. Schroeder, H. Osada, C.T. Walsh, Chem. Biol<\/em>., 2006<\/strong>, 13<\/em>, 1183-1191.<\/p>\n\n\n\n 15. “Nature’s inventory of halogenation catalysts: oxidative strategies predominate,” F.H. Vaillancourt, E. Yeh, D.A. Vosburg, S. Garneau-Tsodikova, C.T. Walsh, Chem. Rev<\/em>., 2006<\/strong>, 106<\/em>, 3364-3378.<\/p>\n\n\n\n 14. “Non-uniformly sampled double-TROSY hNcaNH experiments for NMR sequential assignments of large proteins,” D.P. Frueh, Z.Y.J. Sun, D.A. Vosburg, C.T. Walsh, J.C. Hoch, G. Wagner, J. Am. Chem. Soc<\/em>., 2006<\/strong>, 128<\/em>, 5757-5763.<\/p>\n\n\n\n 13.\u201cDichlorination and bromination of a threonyl-S<\/em>-carrier protein by the non-heme Fe(II) halogenase SyrB2,\u201d F.H. Vaillancourt, D.A. Vosburg, C.T. Walsh, ChemBioChem, <\/em>2006<\/strong>, 7<\/em>, 748-752.<\/p>\n\n\n\n 12. “Determination of all nOes in1<\/sup>H-13<\/sup>C-Me-ILV-U-2<\/sup>H-15<\/sup>N proteins with two time-shared experiments,” D.P. Frueh, D.A. Vosburg, C.T. Walsh, G. Wagner, J. Biomol. NMR,<\/em> <\/strong>2006<\/strong>, 34<\/em>, 31-40.<\/p>\n\n\n\n 11. “Cryptic chlorination by a non-heme iron enzyme during cyclopropyl amino acid biosynthesis,” F.J. Vaillancourt, E. Yeh, D.A. Vosburg, S.E. O’Connor, C.T. Walsh, Nature,<\/em> <\/strong>2005<\/strong>, 436<\/em>, 1191-1194 (highlighted on page 1094 of same issue).<\/p>\n\n\n\n 10. “Nature’s assembly line logic for natural products,” C.T. Walsh, R.G. Kruger, D.A. Vosburg, Chemtracts,<\/em> <\/strong>2005<\/strong>, 18<\/em>, 307-320.<\/p>\n\n\n\n 9. “Natural product biosynthetic assembly lines: prospects and challenges for reprogramming,” D.A. Vosburg, C.T. Walsh, Ernst-Schering Res. Found. Workshop, <\/em>2005<\/strong>, 51<\/em>, 261-284.<\/p>\n\n\n\n 8. “An enantioselective synthesis of FR182877 provides a chemical rationalization of its structure and affords multigram quantities of its direct precursor,” C.D. Vanderwal, D.A. Vosburg, S. Weiler, E.J. Sorensen, J. Am. Chem. Soc<\/em>., 2003<\/strong>, 125<\/em>, 5393-5407.<\/p>\n\n\n\n 7. “Concise stereocontrolled routes to fumagillol, fumagillin, and TNP-470,” D.A. Vosburg, S. Weiler, E.J. Sorensen, Chirality,<\/em> <\/strong>2003<\/strong>, 15<\/em>, 156-166.<\/p>\n\n\n\n 6. “A synthesis of (+)-FR182877 featuring tandem transannular Diels-Alder reactions inspired by a postulated biogenesis,” D.A. Vosburg, C.D. Vanderwal, E.J. Sorensen, J. Am. Chem. Soc<\/em>. 2002<\/strong>, 124<\/em>, 4552-4553.<\/p>\n\n\n\n 5. “Intramolecular allenolate acylations in studies toward a synthesis of FR182877,” C.D. Vanderwal, D.A. Vosburg, E.J. Sorensen, Org. Lett<\/em>., 2001<\/strong>,3<\/em>, 4307-4310.<\/p>\n\n\n\n 4. “Intramolecular hetero Diels-Alder routes to \u03b3-carboline alkaloids,” S.A. Snyder, D.A. Vosburg, M.G. Jarvis, J.H. Markgraf, Tetrahedron,<\/em> <\/strong>2000<\/strong>, 56<\/em>, 5329-5335.<\/p>\n\n\n\n 3. “Postulated biogenesis of WS9885B and progress toward an enantioselective synthesis,” C.D. Vanderwal, D.A. Vosburg, S. Weiler, E.J. Sorensen, E.J., Org. Lett<\/em>., 1999<\/strong>, 1<\/em>, 645-648.<\/p>\n\n\n\n
49. \u201cA pyridine cyclization cascade with and without dichloromethane<\/a>,\u201d N.D. O\u2019Connor, T.K. Gasteazoro, L.N. Stemple, L. Zhu, S.D. Brucks, D.A.\u00a0Vosburg,\u00a0J. Chem. Educ.<\/em>\u00a02025<\/strong>,\u00a0102<\/em>, 5269-5272.<\/p>\n\n\n\n