David A. Vosburg Publications
Professor Vosburg’s Chemistry Publication List
50. 鈥�,鈥� D.A.听Vosburg,听Sustainability & Circularity NOW听2026,听3, a28148200.
49. 鈥�,鈥� N.D. O鈥機onnor, T.K. Gasteazoro, L.N. Stemple, L. Zhu, S.D. Brucks, D.A.听Vosburg,听J. Chem. Educ.听2025,听102, 5269-5272.
48. 鈥�,鈥� A. Milo, L. Chen, K.A. Grice, D.A. Vosburg, J. Chem. Educ. 2025, 102, 2261-2267.
47. 鈥�,鈥� 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. 2025, 15, 102191.
46. 鈥�,鈥� J.H. Ho, G.H. Miller, K.K. Chung, S.D. Neibert, G.L. Beutner, D.A. Vosburg, Org. Lett. 2024, 26, 8904-8909.
45. 鈥�,鈥� N.R. Luis, K.K. Chung, M.R. Hickey, Z. Lin, G.L. Beutner, D.A. Vosburg, Org. Lett. 2024, 26, 2745-2750.
44. 鈥�,鈥� O.W.M. Baldwin, L.H. Conrad-Marut, G.L. Beutner, D.A. Vosburg, J. Chem. Educ., 2022, 99, 3747-3751.
43. 鈥�,鈥� M. Lee, N.J. Vosburg, E.A. Shimizu, M.A. Renter铆a-G贸mez, R. G谩mez-Monta帽o, D.A. Vosburg, J. Chem. Educ., 2022, 99, 2399-2402.
42. “,” D.A. Vosburg, J. Res. Pract. Coll. Teach., 2021, 6.
41. 鈥�,鈥� D.A. Vosburg, InChemistry Education for a Sustainable Society. Vol 2: Innovations in Undergraduate Curricula, ed. S.O. Obare, C.H. Middlecamp, K.E. Peterman, Washington, DC: American Chemical Society, 2020, pp. 63-73.
40. 鈥�,鈥� J. Cervantes-Gonz谩lez, D.A. Vosburg, S.E. Mora-Rodriguez, M.A. V谩zquez, L.G. Zepeda, C. Villegas G贸mez, S. Lagunas Rivera, ChemCatChem, 2020, 12, 3811-3827.
39. 鈥� Reinvigorating general chemistry by connecting chemistry and society,鈥� K.M. Van Heuvelen, G.W. Daub, L.N. Hawkins, A.R. Johnson, H. Van Ryswyk, D.A. Vosburg, J. Chem. Educ., 2020, 97, 925-933.
38. 鈥�,鈥� 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, 2019,9, 1-28.
37. 鈥�,鈥� M.A. Renter铆a-G贸mez, A., Islas-J谩come, S.G. Pharande, D.A. Vosburg, R. G谩mez-Monta帽o, Front. Chem., 2019, 7, 546.
36. 鈥�,鈥� E.A. Shimizu, B. Cory, J. Hoang, G.G. Castro, M.E. Jung, D.A. Vosburg, J. Chem. Educ., 2019, 96, 998-1001.
35. 鈥�,鈥� S.E. Kearney, G. Zahor谩nszky-K艖halmi, 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., 2018, 4, 1727-1741.
34. 鈥�,鈥� K.J. Kron, M. Kosich, R.J. Cave, D.A. Vosburg, J. Org. Chem., 2018, 83, 10941-10947.
33. 鈥�,鈥� E.B. Go, S.P. Wetzler, L.J. Kim, A.Y. Chang, D.A. Vosburg, Tetrahedron, 2016, 72, 3790-3794.
32.鈥�,鈥� E.B. Go, V. Srisuknimit, S.L. Cheng, D.A. Vosburg, J. Chem. Educ., 2016, 93, 368-371. Featured on the
31. 鈥�,鈥� E.D. Nacsa, B.C. Fielder, S.P. Wetzler, V. Srisuknimit, J.P. Litz, M.J. Van Vleet, K. Quach, D.A. Vosburg, Synthesis, 2015, 47, 2599-2602. Featured in and in “,” Brill, Z.G., Condakes, M.L., Ting, C.P., Maimone, T.J., Chem. Rev., 2017, 117, 11753-11795).
30.鈥�,鈥� T.J. Aldrich, P.E. Rolshausen, M.C. Roper, J.M. Reader, M.J. Steinhaus, J. Rapicavoli, D.A. Vosburg, K.N. Maloney, Phytochemistry, 2015, 116, 130-137, DOI: 10.1016/j.phytochem.2015.03.015.
29. 鈥�,鈥� Q. Gan. T.K. Ronson, D.A. Vosburg, J.D. Thoburn, J.R. Nitschke, J. Am. Chem. Soc., 2015, 137, 1770-1773.
28. 鈥溾��,鈥� A.L. Patterson, M.D. May, B.J. Visser, A.A. Kislukhin, D.A. Vosburg, J. Chem. Educ., 2013, 90, 1685-1687.
27. 鈥溾��,鈥� B.H. Lipshutz, Z. Boskovic, C.S. Crowe, V.K. Davis, H.C. Whittemore, D.A. Vosburg, A.G. Wenzel, J. Chem. Educ., 2013, 90, 1514-1517.
26.鈥�,鈥� K.K. Wan, C.D. Evans-Klock, B.C. Fielder, D.A. Vosburg, Synthesis, 2013,45, 1541-1545.
25. 鈥淕reen chemistry and biochemistry,鈥� Vosburg, D.A., In Chemistry for Changing Times, J.W. Hill, T.W. McCreary, D.K. Kolb, 13th edition. New York: Pearson, 2012, p. 467.
24. 鈥�,鈥� A.D. Cunningham, E.Y. Ham, D.A. Vosburg, J. Chem. Educ., 2011,88, 322-324.
23. 鈥�,鈥� K.K. Wan, J.P. Litz, D.A. Vosburg, Tetrahedron Asymm., 2010,21, 2425-2428.
22. 鈥�,鈥� R.T. Nishimura, C.H. Giammanco, D.A. Vosburg, J. Chem. Educ., 2010,87, 526-527.
21. 鈥�,鈥� T.C. Wong, C.M. Sultana, D.A. Vosburg, J. Chem. Educ., 2010,87, 194-195.
20. 鈥�,鈥� K.C. Morrison, J.P. Litz, K.P. Scherpelz, D.P. Dossa, D.A. Vosburg, Org. Lett., 2009,11, 2217-2218, (highlighted in 鈥�,鈥� T. Newhouse, P.S. Baran, R.W. Hoffmann, Chem. Soc. Rev., 2009, 38, 3010-3021).
19. 鈥�,鈥� D.A. Vosburg, J. Chem. Educ., 2008, 85, 1519-1523. Highlighted in “,” A.W. Clauss, on page 1523 of same issue.
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, Nature, 2008, 454, 903-906 (highlighted on pages 832-833 of same issue).
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, 2007, 46, 359-368.
16. “Enzymatic generation of the antimetabolite 纬,纬-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., 2006, 13, 1183-1191.
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., 2006, 106, 3364-3378.
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., 2006, 128, 5757-5763.
13.鈥淒ichlorination and bromination of a threonyl-S-carrier protein by the non-heme Fe(II) halogenase SyrB2,鈥� F.H. Vaillancourt, D.A. Vosburg, C.T. Walsh, ChemBioChem, 2006, 7, 748-752.
12. “Determination of all nOes in1H-13C-Me-ILV-U-2H-15N proteins with two time-shared experiments,” D.P. Frueh, D.A. Vosburg, C.T. Walsh, G. Wagner, J. Biomol. NMR, 2006, 34, 31-40.
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, 2005, 436, 1191-1194 (highlighted on page 1094 of same issue).
10. “Nature’s assembly line logic for natural products,” C.T. Walsh, R.G. Kruger, D.A. Vosburg, Chemtracts, 2005, 18, 307-320.
9. “Natural product biosynthetic assembly lines: prospects and challenges for reprogramming,” D.A. Vosburg, C.T. Walsh, Ernst-Schering Res. Found. Workshop, 2005, 51, 261-284.
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., 2003, 125, 5393-5407.
7. “Concise stereocontrolled routes to fumagillol, fumagillin, and TNP-470,” D.A. Vosburg, S. Weiler, E.J. Sorensen, Chirality, 2003, 15, 156-166.
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. 2002, 124, 4552-4553.
5. “Intramolecular allenolate acylations in studies toward a synthesis of FR182877,” C.D. Vanderwal, D.A. Vosburg, E.J. Sorensen, Org. Lett., 2001,3, 4307-4310.
4. “Intramolecular hetero Diels-Alder routes to 纬-carboline alkaloids,” S.A. Snyder, D.A. Vosburg, M.G. Jarvis, J.H. Markgraf, Tetrahedron, 2000, 56, 5329-5335.
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., 1999, 1, 645-648.
2. “A concise synthesis of fumagillol,” D.A. Vosburg, W. Weiler, E.J. Sorensen, Angew. Chem., 1999,111, 1024-1027 and Angew. Chem. Int. Ed., 1999, 38, 971-974.
1. “A concise route to isocanthin-6-one,” J.H. Markgraf, S.A. Snyder, D.A. Vosburg, Tetrahedron Lett., 1998, 39, 1111-1112.
Professor Vosburg鈥檚 Science & Religion Publication List
6. 鈥淣avigating Knowledge: Creativity that Delights鈥� D.A. Vosburg, In, ed. Hannah Eagleson, InterVarsity, 2021, pp. 23-25.
5. 鈥�,鈥� D.A. Vosburg, Nat. y Tras. (Rev. RYPC), 2020.
4. 鈥淗ow can we engage origins questions well?鈥� D.A. Vosburg, In Science & Faith: Student Questions Explored, ed. Hannah Eagleson, Peabody, MA: Hendrickson, 2019, pp. 51-54.
3. Jesus, Beginnings, and Science: A Guide for Group Conversation, D.A. Vosburg, K. Vosburg, Farmville, VA: Pier Press, 2017.
2. 鈥淲hat does Christ have to do with chemistry?鈥� D.A. Vosburg, In Christians and Evolution: Christian Scholars Change Their Mind, ed. R.J. Berry, Oxford: Monarch Books, 2014, pp. 245-259.
1. “” study guide, D.A. Vosburg, Highway Media, 2012.