| Year |
Citation |
Score |
| 2019 |
Rentería-Gómez MA, Islas-Jácome A, Pharande SG, Vosburg DA, Gámez-Montaño R. Synthesis of Tris-Heterocycles via a Cascade IMCR/Aza Diels-Alder + CuAAC Strategy. Frontiers in Chemistry. 7: 546. PMID 31448260 DOI: 10.3389/Fchem.2019.00546 |
0.461 |
|
| 2019 |
Shimizu EA, Cory B, Hoang J, Castro GG, Jung ME, Vosburg DA. Aqueous Dearomatization/Diels–Alder Cascade to a Grandifloracin Precursor Journal of Chemical Education. 96: 998-1001. DOI: 10.1021/Acs.Jchemed.8B00857 |
0.3 |
|
| 2018 |
Kearney SE, Zahoránszky-Kőhalmi G, Brimacombe KR, Henderson MJ, Lynch C, Zhao T, Wan KK, Itkin Z, Dillon C, Shen M, Cheff DM, Lee TD, Bougie D, Cheng K, Coussens NP, ... ... Vosburg DA, et al. Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space. Acs Central Science. 4: 1727-1741. PMID 30648156 DOI: 10.1021/Acscentsci.8B00747 |
0.656 |
|
| 2018 |
Kron KJ, Kosich M, Cave RJ, Vosburg DA. Divergent Diels-Alder Reactions in the Biosynthesis and Synthesis of Endiandric-Type Tetracycles: A Computational Study. The Journal of Organic Chemistry. PMID 30113843 DOI: 10.1021/Acs.Joc.8B01594 |
0.408 |
|
| 2015 |
Aldrich TJ, Rolshausen PE, Roper MC, Reader JM, Steinhaus MJ, Rapicavoli J, Vosburg DA, Maloney KN. Radicinin from Cochliobolus sp. inhibits Xylella fastidiosa, the causal agent of Pierce's Disease of grapevine. Phytochemistry. 116: 130-7. PMID 25892412 DOI: 10.1016/J.Phytochem.2015.03.015 |
0.302 |
|
| 2015 |
Nacsa ED, Fielder BC, Wetzler SP, Srisuknimit V, Litz JP, Van Vleet MJ, Quach K, Vosburg DA. Direct, Biomimetic Synthesis of (+)-Artemone via a Stereoselective, Organocatalytic Cyclization Synthesis (Germany). 47: 2599-2602. DOI: 10.1055/S-0034-1380684 |
0.445 |
|
| 2015 |
Go EB, Wetzler SP, Kim LJ, Chang AY, Vosburg DA. Concise, diastereoconvergent synthesis of endiandric-type tetracycles by iterative cross coupling Tetrahedron. DOI: 10.1016/J.Tet.2016.02.040 |
0.422 |
|
| 2013 |
Lipshutz BH, Boškovi? Z, Crowe CS, Davis VK, Whittemore HC, Vosburg DA, Wenzel AG. "Click" and Olefin Metathesis Chemistry in Water at Room Temperature Enabled by Biodegradable Micelles. Journal of Chemical Education. 90. PMID 24324282 DOI: 10.1021/Ed300893U |
0.359 |
|
| 2013 |
Wan KK, Evans-Klock CD, Fielder BC, Vosburg DA. Synthesis of cis- and trans -davanoids: Artemone, hydroxydavanone, isodavanone, and nordavanone Synthesis (Germany). 45: 1541-1545. DOI: 10.1055/S-0033-1338429 |
0.391 |
|
| 2011 |
Cunningham AD, Ham EY, Vosburg DA. Chemoselective reactions of citral: Green syntheses of natural perfumes for the undergraduate organic laboratory Journal of Chemical Education. 88: 322-324. DOI: 10.1021/Ed100539M |
0.443 |
|
| 2010 |
Nishimura RT, Giammanco CH, Vosburg DA. Green, enzymatic syntheses of divanillin and diapocynin for the organic, biochemistry, or advanced general chemistry laboratory Journal of Chemical Education. 87: 526-527. DOI: 10.1021/Ed8001607 |
0.367 |
|
| 2010 |
Wong TC, Sultana CM, Vosburg DA. A green, enantioselective synthesis of warfarin for the undergraduate organic laboratory Journal of Chemical Education. 87: 194-195. DOI: 10.1021/Ed800040M |
0.401 |
|
| 2010 |
Wan KK, Litz JP, Vosburg DA. Two-step, stereoselective synthesis of linalyl oxides by asymmetric allylic O-alkylation Tetrahedron Asymmetry. 21: 2425-2428. DOI: 10.1016/J.Tetasy.2010.08.011 |
0.328 |
|
| 2009 |
Morrison KC, Litz JP, Scherpelz KP, Dossa PD, Vosburg DA. A concise, biomimetic total synthesis of (+)-davanone. Organic Letters. 11: 2217-8. PMID 19366191 DOI: 10.1021/Ol900697W |
0.468 |
|
| 2008 |
Frueh DP, Arthanari H, Koglin A, Vosburg DA, Bennett AE, Walsh CT, Wagner G. Dynamic thiolation-thioesterase structure of a non-ribosomal peptide synthetase. Nature. 454: 903-6. PMID 18704088 DOI: 10.1038/Nature07162 |
0.425 |
|
| 2007 |
Kelly WL, Boyne MT, Yeh E, Vosburg DA, Galoni? DP, Kelleher NL, Walsh CT. Characterization of the aminocarboxycyclopropane-forming enzyme CmaC. Biochemistry. 46: 359-68. PMID 17209546 DOI: 10.1021/Bi061930J |
0.687 |
|
| 2006 |
Ueki M, Galoni? DP, Vaillancourt FH, Garneau-Tsodikova S, Yeh E, Vosburg DA, Schroeder FC, Osada H, Walsh CT. Enzymatic generation of the antimetabolite gamma,gamma-dichloroaminobutyrate by NRPS and mononuclear iron halogenase action in a streptomycete. Chemistry & Biology. 13: 1183-91. PMID 17114000 DOI: 10.1016/J.Chembiol.2006.09.012 |
0.677 |
|
| 2006 |
Vaillancourt FH, Yeh E, Vosburg DA, Garneau-Tsodikova S, Walsh CT. Nature's inventory of halogenation catalysts: oxidative strategies predominate. Chemical Reviews. 106: 3364-78. PMID 16895332 DOI: 10.1021/Cr050313I |
0.647 |
|
| 2006 |
Frueh DP, Sun ZY, Vosburg DA, Walsh CT, Hoch JC, Wagner G. Non-uniformly sampled double-TROSY hNcaNH experiments for NMR sequential assignments of large proteins. Journal of the American Chemical Society. 128: 5757-63. PMID 16637644 DOI: 10.1021/Ja0584222 |
0.415 |
|
| 2006 |
Vaillancourt FH, Vosburg DA, Walsh CT. Dichlorination and bromination of a threonyl-S-carrier protein by the non-heme Fe(II) halogenase SyrB2. Chembiochem : a European Journal of Chemical Biology. 7: 748-52. PMID 16528784 DOI: 10.1002/Cbic.200500480 |
0.394 |
|
| 2006 |
Frueh DP, Vosburg DA, Walsh CT, Wagner G. Determination of all nOes in 1H-13C-Me-ILV-U-2H-15N proteins with two time-shared experiments. Journal of Biomolecular Nmr. 34: 31-40. PMID 16505962 DOI: 10.1007/S10858-005-5338-4 |
0.394 |
|
| 2005 |
Vaillancourt FH, Yeh E, Vosburg DA, O'Connor SE, Walsh CT. Cryptic chlorination by a non-haem iron enzyme during cyclopropyl amino acid biosynthesis. Nature. 436: 1191-4. PMID 16121186 DOI: 10.1038/Nature03797 |
0.71 |
|
| 2005 |
Vosburg DA, Walsh CT. Natural product biosynthetic assembly lines: prospects and challenges for reprogramming. Ernst Schering Research Foundation Workshop. 261-84. PMID 15645725 |
0.382 |
|
| 2003 |
Vanderwal CD, Vosburg DA, Weiler S, Sorensen EJ. An enantioselective synthesis of FR182877 provides a chemical rationalization of its structure and affords multigram quantities of its direct precursor. Journal of the American Chemical Society. 125: 5393-407. PMID 12720453 DOI: 10.1021/Ja021472B |
0.726 |
|
| 2003 |
Vosburg DA, Weiler S, Sorensen EJ. Concise stereocontrolled routes to fumagillol, fumagillin, and TNP-470. Chirality. 15: 156-66. PMID 12520508 DOI: 10.1002/Chir.10181 |
0.606 |
|
| 2002 |
Vosburg DA, Vanderwal CD, Sorensen EJ. A synthesis of (+)-FR182877, featuring tandem transannular Diels-Alder reactions inspired by a postulated biogenesis. Journal of the American Chemical Society. 124: 4552-3. PMID 11971689 DOI: 10.1021/Ja025885O |
0.722 |
|
| 2001 |
Vanderwal CD, Vosburg DA, Sorensen EJ. Intramolecular allenolate acylations in studies toward a synthesis of FR182877. Organic Letters. 3: 4307-10. PMID 11784204 DOI: 10.1021/Ol016994V |
0.726 |
|
| 2001 |
Vanderwal CD, Vosburg DA, Sorensen EJ. Intramolecular allenolate acylations in studies toward a synthesis of FR182877 Organic Letters. 3: 4307-4310. DOI: 10.1021/ol016994v |
0.698 |
|
| 2000 |
Snyder SA, Vosburg DA, Jarvis MG, Markgraf JH. Intramolecular hetero Diels-Alder routes to γ-carboline alkaloids Tetrahedron. 56: 5329-5335. DOI: 10.1016/S0040-4020(00)00468-3 |
0.414 |
|
| 1999 |
Vosburg DA, Weiler S, Sorensen EJ. A Concise Synthesis of Fumagillol. Angewandte Chemie (International Ed. in English). 38: 971-974. PMID 29711854 DOI: 10.1002/(Sici)1521-3773(19990401)38:7<971::Aid-Anie971>3.0.Co;2-W |
0.555 |
|
| 1999 |
Vanderwal CD, Vosburg DA, Weiler S, Sorensen EJ. Postulated biogenesis of WS9885B and progress toward an enantioselective synthesis. Organic Letters. 1: 645-8. PMID 10823194 DOI: 10.1021/Ol990723R |
0.692 |
|
| 1999 |
Vosburg DA, Weiler S, Sorensen EJ. A concise synthesis of fumagillol Angewandte Chemie - International Edition. 38: 971-974. DOI: 10.1002/(SICI)1521-3773(19990401)38:7<971::AID-ANIE971>3.0.CO;2-W |
0.556 |
|
| 1999 |
Vosburg DA, Weiler S, Sorensen EJ. Eine kurze Synthese von Fumagillol Angewandte Chemie. 111: 1024-1027. DOI: 10.1002/(Sici)1521-3757(19990401)111:7<1024::Aid-Ange1024>3.0.Co;2-S |
0.562 |
|
| 1998 |
Markgraf JH, Snyder SA, Vosburg DA. A concise route to isocanthin-6-one Tetrahedron Letters. 39: 1111-1112. DOI: 10.1016/S0040-4039(97)10794-8 |
0.393 |
|
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