| Year |
Citation |
Score |
| 2020 |
Ma R, Gung BW. Transition states of the gold-catalyzed transannular [4+3] cycloaddition reactions: A computational study Tetrahedron. 76: 130840. DOI: 10.1016/J.Tet.2019.130840 |
0.399 |
|
| 2019 |
Ma R, Yang J, Kelley S, Gung BW. NHC–Au(I) catalyzed enantioselective intramolecular [4+3] cycloaddition of furan propargyl esters Journal of Organometallic Chemistry. 898: 120865. DOI: 10.1016/J.Jorganchem.2019.07.016 |
0.379 |
|
| 2016 |
Gung BW, Holmes MR, Jones CA, Ma R, Barnes CL. Structure–enantioselectivity correlation in NHC–Au(I) catalysis for 1,6-enynecyclizations Tetrahedron Letters. 57: 3912-3915. DOI: 10.1016/J.Tetlet.2016.07.046 |
0.384 |
|
| 2014 |
Holmes MR, Manganaro JF, Barnes CL, Gung BW. Synthesis and characterization of novel chiral [(NHC)Au(I)Cl] complexes: Featuring ortho-biphenyl substituents Journal of Organometallic Chemistry. DOI: 10.1016/J.Jorganchem.2015.02.034 |
0.358 |
|
| 2013 |
Conyers RC, Gung BW. Gold(I)-catalyzed divergence in the preparation of bicyclic enol esters: from exclusively [3C+2C]-cycloaddition reactions to exclusive formation of vinylcyclopropanes. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 654-64. PMID 23150124 DOI: 10.1002/chem.201202881 |
0.305 |
|
| 2010 |
Gung BW, Emenike BU, Lewis M, Kirschbaum K. Quantification of CH···π interactions: implications on how substituent effects influence aromatic interactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 12357-62. PMID 20853288 DOI: 10.1002/Chem.201001362 |
0.341 |
|
| 2010 |
Gung BW, Emenike BU, Alverez CN, Rakovan J, Kirschbaum K, Jain N. Relative substituent position on the strength of pi-pi stacking interactions. Tetrahedron Letters. 51: 1648-1650. PMID 20209117 DOI: 10.1016/J.Tetlet.2009.12.095 |
0.362 |
|
| 2010 |
Gung BW, Craft DT, Bailey LN, Kirschbaum K. Gold-catalyzed transannular [4+3] cycloaddition reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 639-44. PMID 19937623 DOI: 10.1002/Chem.200902185 |
0.352 |
|
| 2010 |
Gung BW, Bailey LN, Craft DT, Barnes CL, Kirschbaum K. Preparation and characterization of two new N-heterocyclic carbene gold(I) complexes and comparison of their catalytic activity to Au(IPr)Cl Organometallics. 29: 3450-3456. DOI: 10.1021/Om100504Z |
0.34 |
|
| 2009 |
Gung BW. Total synthesis of polyyne natural products Comptes Rendus Chimie. 12: 489-505. DOI: 10.1016/J.Crci.2008.08.014 |
0.315 |
|
| 2008 |
Gung BW, Omollo AO. First Total Synthesis of the Potent Anticancer Natural Product Dideoxypetrosynol A: Preparation of the "Skipped" (Z)-Enediyne Moiety by Oxidative Coupling of Homopropargyl Phosphonium Ylide. European Journal of Organic Chemistry. 2008: 4790-4795. PMID 23519828 DOI: 10.1002/Ejoc.200800593 |
0.357 |
|
| 2008 |
Craft DT, Gung BW. The first transannular [4+3] cycloaddition reaction: synthesis of the ABCD ring structure of cortistatins. Tetrahedron Letters. 49: 5931-5934. PMID 19812680 DOI: 10.1016/J.Tetlet.2008.07.155 |
0.387 |
|
| 2008 |
Amicangelo JC, Gung BW, Irwin DG, Romano NC. Ab initio study of substituent effects in the interactions of dimethyl ether with aromatic rings. Physical Chemistry Chemical Physics : Pccp. 10: 2695-705. PMID 18464984 DOI: 10.1039/B718722J |
0.369 |
|
| 2008 |
Gung BW, Wekesa F, Barnes CL. Stacking interactions between nitrogen-containing six-membered heterocyclic aromatic rings and substituted benzene: Studies in solution and in the solid state Journal of Organic Chemistry. 73: 1803-1808. PMID 18266384 DOI: 10.1021/Jo702354X |
0.397 |
|
| 2008 |
Gung BW, Omollo AO. Total synthesis of (+)- and (-)-duryne: a potent anticancer agent from the marine sponge Cribrochalina dura. Establishment of the central double bond geometry and the absolute configuration of the chiral centers. The Journal of Organic Chemistry. 73: 1067-70. PMID 18184009 DOI: 10.1021/Jo702399J |
0.428 |
|
| 2008 |
Gung BW, Zou Y, Xu Z, Amicangelo JC, Irwin DG, Ma S, Zhou HC. Quantitative study of interactions between oxygen lone pair and aromatic rings: substituent effect and the importance of closeness of contact. The Journal of Organic Chemistry. 73: 689-93. PMID 18081348 DOI: 10.1021/Jo702170J |
0.396 |
|
| 2007 |
Gung BW, Xue X, Zou Y. Enthalpy (DeltaH) and entropy (DeltaS) for pi-stacking interactions in near-sandwich configurations: relative importance of electrostatic, dispersive, and charge-transfer effects. The Journal of Organic Chemistry. 72: 2469-75. PMID 17338571 DOI: 10.1021/Jo062526T |
0.365 |
|
| 2006 |
Gung BW, Amicangelo JC. Substituent effects in C6F6-C6H5X stacking interactions. The Journal of Organic Chemistry. 71: 9261-70. PMID 17137351 DOI: 10.1021/Jo061235H |
0.319 |
|
| 2006 |
Gung BW, Fox RM, Falconer R, Shissler D. Total synthesis of two naturally occurring polyacetylenic glucosides (-)-bidensyneoside A1 and B, and an analogue of (-)-bidensyneoside C Tetrahedron Asymmetry. 17: 40-46. DOI: 10.1016/J.Tetasy.2005.10.027 |
0.306 |
|
| 2005 |
Gung BW, Patel M, Xue X. A threshold for charge transfer in aromatic interactions? A quantitative study of pi-stacking interactions. The Journal of Organic Chemistry. 70: 10532-7. PMID 16323868 DOI: 10.1021/Jo051808A |
0.325 |
|
| 2005 |
Gung BW, Xue X, Reich HJ. Off-center oxygen-arene interactions in solution: a quantitative study. The Journal of Organic Chemistry. 70: 7232-7. PMID 16122242 DOI: 10.1021/Jo050874+ |
0.377 |
|
| 2005 |
Gung BW, Xue X, Reich HJ. The strength of parallel-displaced arene-arene interactions in chloroform. The Journal of Organic Chemistry. 70: 3641-4. PMID 15845001 DOI: 10.1021/Jo050049T |
0.406 |
|
| 2004 |
Gung BW, Kumi G. Total synthesis of (S)-(-)-(E)-15,16-dihydrominquartynoic acid: a highly potent anticancer agent. The Journal of Organic Chemistry. 69: 3488-92. PMID 15132560 DOI: 10.1021/Jo049920G |
0.351 |
|
| 2004 |
Gung BW. Additions of Allyl, Allenyl, and Propargylstannanes to Aldehydes and Imines Organic Reactions. 1-113. DOI: 10.1002/0471264180.Or064.01 |
0.387 |
|
| 2003 |
Gung BW, Kumi G. Remarkable reactivity difference in oxygen-substituted versus non-oxygen-substituted bromoalkynes in Cu(I)-catalyzed cross-coupling reactions: total synthesis of (-)-S-18-hydroxyminquartynoic acid. The Journal of Organic Chemistry. 68: 5956-60. PMID 12868932 DOI: 10.1021/Jo0344900 |
0.361 |
|
| 2003 |
Gung BW, Xue X, Knatz N, Marshall JA. Addition of chiral allenylzinc reagent to acetaldehyde: Diastereotopic cyclic transition states with a tetrahedral zinc atom located by ab initio and density functional theory Organometallics. 22: 3158-3163. DOI: 10.1021/Om030220W |
0.332 |
|
| 2003 |
Gung BW, Xue X, Roush WR. The Origin of Diastereofacial Control in Allylboration Reactions Using Tartrate Ester Derived Allylboronates: Attractive Interactions between the Lewis Acids Coordinated Aldehyde Carbonyl Group and an Ester Carbonyl Oxygen [J. Am. Chem. Soc.2002,124, 10692−10697]. Journal of the American Chemical Society. 125: 3668-3668. DOI: 10.1021/Ja025125D |
0.365 |
|
| 2002 |
Gung BW, Xue X, Roush WR. The origin of diastereofacial control in allylboration reactions using tartrate ester derived allylboronates: attractive interactions between the Lewis acid coordinated aldehyde carbonyl group and an ester carbonyl oxygen. Journal of the American Chemical Society. 124: 10692-7. PMID 12207523 DOI: 10.1021/Ja026373C |
0.401 |
|
| 2002 |
Gung BW, Dickson H. Total synthesis of (-)-minquartynoic acid: an anti-cancer, anti-HIV natural product. Organic Letters. 4: 2517-9. PMID 12123365 DOI: 10.1021/Ol026145N |
0.323 |
|
| 1999 |
Gung BW, MacKay JA, Zou D. Substituent Effect on Intramolecular Hydrogen Bonding in beta-Amino Acid-Containing Polyamides. The Journal of Organic Chemistry. 64: 700-706. PMID 11674135 DOI: 10.1021/Jo980310O |
0.378 |
|
| 1999 |
Gung BW. Structure Distortions in Heteroatom-Substituted Cyclohexanones, Adamantanones, and Adamantanes: Origin of Diastereofacial Selectivity Chemical Reviews. 99: 1377-1386. DOI: 10.1021/Cr980365Q |
0.312 |
|
| 1997 |
Gung BW, Zhu Z. Different Folding Patterns of Two Similar Triamides: A Sharp Contrast in Their Intramolecular Amide-Amide Hydrogen-Bonding Propensity. The Journal of Organic Chemistry. 62: 2324-2325. PMID 11671559 DOI: 10.1021/Jo962205P |
0.303 |
|
| 1996 |
Gung BW, Wolf MA. Distortion in the structures of 5-azaadamantanone and its N-oxide: Implication on diastereofacial selectivity Journal of Organic Chemistry. 61: 232-236. DOI: 10.1021/Jo9517297 |
0.308 |
|
| 1996 |
Gung BW, Zhu Z. Enhanced intramolecular amide-amide hydrogen bonding through cooperativity Tetrahedron Letters. 37: 2189-2192. DOI: 10.1016/0040-4039(96)00256-0 |
0.345 |
|
| 1995 |
Gung BW, Zhu Z, Fouch RA. Transition state of the silicon-directed aldol reaction: An ab initio molecular orbital study Journal of Organic Chemistry. 60: 2860-2864. DOI: 10.1021/Jo00114A041 |
0.345 |
|
| 1995 |
Gung BW, Melnick JP, Wolf MA, King A. Steric and electronic effects in conformational preferences of C1-oxygenated chiral alkenes Journal of Organic Chemistry. 60: 1947-1951. DOI: 10.1021/Jo00112A012 |
0.346 |
|
| 1995 |
Gung BW, Zhu Z, Fouch RA. Conformational study of 1,5-hexadiene and 1,5-diene-3,4-diols Journal of the American Chemical Society. 117: 1783-1788. DOI: 10.1021/Ja00111A016 |
0.313 |
|
| 1994 |
Gung BW, Melnick JP, Wolf MA, Marshall JA, Beaudoin S. Profound Preference for the CO-Eclipsed Conformation in 1,5-Dienyl-3,4-diols: The Origin of .pi.-Facial Selectivity Journal of Organic Chemistry. 59: 5609-5613. DOI: 10.1021/Jo00098A018 |
0.375 |
|
| 1994 |
Gung BW, Wolf MA, Karipides A, Mareska DA. Origin of the Conformational Mobility for Tetrahydro-4-pyranone: An ab Initio MO Study Journal of Organic Chemistry. 59: 4899-4903. DOI: 10.1021/Jo00096A036 |
0.305 |
|
| 1994 |
Gung BW, Wolf MA, Mareska DA, Brockway CA. A Variable-Temperature NMR Study of Several 2-Aryl-3-methyl-6-methoxytetrahydro-4-pyranones Journal of Organic Chemistry. 59: 4895-4898. DOI: 10.1021/Jo00096A035 |
0.313 |
|
| 1994 |
Gung BW, Gerdeman MS, Fouch RA, Wolf MA. Conformational Studies of Chiral .alpha.,.beta.-Unsaturated Aldehydes The Journal of Organic Chemistry. 59: 4255-4261. DOI: 10.1021/Jo00094A043 |
0.372 |
|
| 1993 |
Gung BW, Wolf MA. Conformational study of chiral alkenes: The influence of protective groups on the relative stability of Ground-State rotational isomers Journal of Organic Chemistry. 58: 7038-7044. DOI: 10.1021/Jo00077A023 |
0.376 |
|
| 1993 |
Gung BW, Francis MB. Diastereofacial selectivity in intramolecular 1,4-conjugate additions: conclusive evidence for the importance of ground-state conformations and the .sigma.* orbital effect Journal of Organic Chemistry. 58: 6177-6179. DOI: 10.1021/Jo00075A006 |
0.326 |
|
| 1993 |
Gung BW, Wolf MA, Ohm K, Peat AJ. Conformational preferences of C1-oxygenated acyclic chiral alkenes: The effect of vinyl and allyl substituents Tetrahedron Letters. 34: 1417-1420. DOI: 10.1016/S0040-4039(00)60307-6 |
0.378 |
|
| 1992 |
Gung BW, Wolf MA. A study of the electronic structures of boron trifluoride complexes with carbonyl compounds by ab initio MO methods The Journal of Organic Chemistry. 57: 1370-1375. DOI: 10.1021/Jo00031A013 |
0.304 |
|
| 1992 |
Gung BW, Karipides A, Wolf MA. X-ray structure of a chiral alkene: direct evidence for CH bond eclipsing CH bond Tetrahedron Letters. 33: 713-716. DOI: 10.1016/S0040-4039(00)77697-0 |
0.349 |
|
| 1991 |
Gung BW, Smith DT, Wolf MA. Remarkable increase in the diastereofacial selectivity of the addition of β-methyl α-(alkoxy)allylstannane to aldehydes: substituent effects on diastereofacial selectivity Tetrahedron Letters. 32: 13-16. DOI: 10.1016/S0040-4039(00)71205-6 |
0.352 |
|
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