{"id":37,"date":"2012-11-29T20:27:45","date_gmt":"2012-11-29T20:27:45","guid":{"rendered":"http:\/\/pages.charlotte.edu\/craig-ogle\/?page_id=37"},"modified":"2013-03-28T15:49:53","modified_gmt":"2013-03-28T15:49:53","slug":"publications","status":"publish","type":"page","link":"https:\/\/pages.charlotte.edu\/craig-ogle\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"
    \n
  1. Steven H. Bertz, Richard A. Hardin, Michael D. Murphy, Craig A. Ogle, Joshua D. Richter and Andy A. Thomas \u201cMinimization of Organocuprate Complexity through Self-Organization: Remarkable Orientation Effect in Mixed Cuprate \u03c0-Complexes”,\u00a0Angewandte Chemie, International Edition<\/a> (2012<\/strong>) 51(11) 2681-5.<\/li>\n
  2. Steven H. Bertz, Richard A. Hardin, Michael D. Murphy, Craig A. Ogle, Joshua D. Richter, and Andy A. Thomas\u00a0\u201cRapid Injection NMR Reveals \u03b73 \u2018\u03c0-Allyl\u2019 CuIII Intermediates in Addition Reactions of Organocuprate Reagents\u201d<\/a>\u00a0Journal of the American Chemical Society<\/span>\u00a0(2012<\/strong>)\u00a0134<\/em>\u00a0(23), 9557\u201360.<\/li>\n
  3. “5-Methoxy-1-(3,4,5-trimethoxyphenyl)-1H<\/em>-indole,” Thomas Blake Monroe, Casey Rimland, Yasamin Moazami, Daniel S. Jones and Craig A. Ogle,\u00a0Acta Crystallographica<\/em>, Volume E66<\/span>, p. o1678. (2010)<\/li>\n
  4. “Tetrakis(4-tert<\/em>-butylbenzyl)silane,”Lauren E. Burnham, Rulla M. Kachlan, Andy A. Thomas, Craig A. Ogle and Daniel S. Jones,\u00a0Acta Crystallographica<\/em>, Volume E66<\/span>, p. o2442. (2010)<\/li>\n
  5. Bertz, Steven H.; Moazami, Yasamin; Murphy, Michael D.; Ogle, Craig A.; Richter, Joshua D.; Thomas, Andy A.,\u00a0Complexes of Gilman Reagents with C-S and C-N Double Bonds: s or p Bonding?<\/a>\u00a0J. Am. Chem. Soc.\u00a0(2010),\u00a0132(28),\u00a09549-9551.<\/li>\n
  6. Steven H. Bertz, Michael D. Murphy, Craig A. Ogle and Andy A. Thomas,\u00a0Organocuprate(III) chemistry: synthesis and reactivity of amido, cyano, phosphido and thiolato ate complexes of copper(III)<\/a>,<\/strong>\u00a0Chem. Commun., 2010,\u00a046, 1255-6.<\/strong><\/li>\n
  7. Erika R. Bartholomew, Steven H. Bertz, Stephen K. Cope, Michael D. Murphy, Craig A. Ogle and Andy A. Thomas,\u00a0Serendipity strikes again\u2014efficient preparation of lithium tetramethylcuprate(III) via rapid injection NMR<\/a>,\u00a0<\/strong>Chem. Commun., 2010,\u00a046, 1253-4.<\/strong><\/li>\n
  8. Methyl 5,6-dimethoxy-1H-indole-2-carboxylate\u00a0<\/a>,\u00a0<\/strong>Monroe, Thomas Blake; Moazami, Yasamin; Jones, Daniel S.; Ogle, Craig A. Acta Crystallographica, Section E: Structure Reports Online (2009) E65(10), o2353.<\/li>\n
  9. (1-Bromonaphthalen-2-yl)acetonitrile\u00a0<\/a>By Harris, Andria D.; Baucom, Amy D.; Brown, Jessica L.; Jones, Daniel S.; Og le, Craig A.\u00a0 Acta Crystallographica, Section E: Structure Reports Online\u00a0(2008),\u00a0E64(7),\u00a0o1284, o1284\/1-o1284\/9.<\/li>\n
  10. E.R. Bartholomew, S.H. Bertz, S. Cope, M. Murphy, and C.A. Ogle, Preparation of s and p-allyl CuIII intermediates in reactions of organocuprate(I) reagents with allylic substrates.\u00a0\u00a0<\/strong>J. Am .Chem. Soc. (2008),\u00a0 130,\u00a0 1244-5.<\/li>\n
  11. Bartholomew, E.R.; Bertz, S.H.; Cope, S.; Dorton, D.C.; Murphy, M.; Ogle, C.A..\u00a0 Neutral organocopper(III) complexes.<\/strong>\u00a0\u00a0Chem. Comm.<\/span>\u00a0(2008),\u00a0 (10),\u00a0 1176-1177.<\/li>\n
  12. Bertz, S.H.; Cope, S.; Dorton, Donna; Murphy, M.; Ogle, C.A..\u00a0\u00a0\u00a0<\/strong>Organocuprate cross-coupling: the central role of the copper(III) intermediate and the importance of the copper(I) precursor.\u00a0\u00a0Angew. Chemie, IE<\/span>\u00a0(2007),\u00a0 46(37),\u00a0 7082-7085.<\/li>\n
  13. Watson, Amanda J.; Cope, Stephen K.; Jones, Daniel S.; Ogle, Craig A..\u00a0\u00a0\u00a0<\/strong>cis-2,2-Dimethyl-1,3-diphenyl-2,3-dihydro-1H-benzo[c]silole.\u00a0Acta. Cryst.<\/span>, Section E: Structure Reports Online\u00a0 (2007),\u00a0 E63(7),\u00a0 o3346.<\/li>\n
  14. Bertz, Steven H.; Cope, Stephen; Murphy, Michael; Ogle, Craig A.; Taylor, Brad J.\u00a0 Rapid\u00a0<\/strong>Injection NMR in Mechanistic Organocopper Chemistry. Preparation of the Elusive Copper(III) Intermediate.\u00a0 Journal of the American Chemical Society\u00a0 (2007),\u00a0 129(23),\u00a0 7208-7209.<\/li>\n
  15. Duong, Luong C.; Cope, Stephen K.; Jones, Daniel S.; Ogle, Craig A..\u00a0\u00a0\u00a0<\/strong>cis-1,2,2,3-Tetraphenyl-2,3-dihydro-1H-2-benzosilole.\u00a0\u00a0\u00a0 Acta Crystallographica, Section E: Structure Reports Online (2006),\u00a0 E62(8),\u00a0 o3574-o3576.<\/li>\n
  16. \u201c1-(3,4,5-trimethoxyphenyl)naphthalene\u201d<\/strong>\u00a0Binita Suthar, Anthony Fowler, Daniel S. Jones, Craig A. Ogle.\u00a0\u00a0Acta. Cryst.<\/span>\u00a0(2005). E61, o607-o608.<\/li>\n
  17. \u201cSubtle factors are important: radical formation and transmetallation in reactions of butyl cuprates with cyclohexyl iodide.\u201d\u00a0\u00a0<\/strong>Bertz, Steven H.; Human, Jason; Ogle, Craig A.; Seagle, Paul.\u00a0 Organic & Biomolecular Chemistry\u00a0 (2005),\u00a0 3(3),\u00a0 392-394.<\/li>\n
  18. \u201cRemarkable Effect of Silyl Groups on Asymmetric Induction in a Conjugate Addition Reaction with O-Methylnorephedrine-Based N-Silylamidocuprates.\u201d\u00a0 Bertz, Steven H.; Ogle, Craig A.; Rastogi, Abhinav.\u00a0\u00a0J. Am .Chem. Soc<\/span>. (2005),\u00a0 127(5),\u00a0 1372-1373.<\/li>\n
  19. \u201cOpening the black box’: oscillations in organocuprate conjugate addition reactions.\u201d<\/strong>\u00a0 Murphy, Michael D.; Ogle, Craig A.; Bertz, Steven H.\u00a0\u00a0Chem. Comm.<\/span>\u00a0(2005),\u00a0\u00a0 (7),\u00a0 854-856.<\/li>\n
  20. \u201c(S)-2-(Methoxydiphenylmethyl)-1-(thiophen-3-ylmethyl)pyrrolidine\u201d\u00a0 Erica Martin, A. Leigh Winfrey, Jason B. Human, C. Zachary Carlin, Daniel S. Jones and Craig A. Ogle\u00a0Acta Cryst.<\/span>\u00a02003, E59, 1970-1.<\/li>\n
  21. \u201cChiral lithiothiophenes as non-transferable ligands in organocuprate conjugate addition reactions.\u201d\u00a0 Ogle, Craig A.; Human, Jason B.\u00a0\u00a0Tetrahedron: Asymmetry<\/span>\u00a0(2003),\u00a0 14(21),\u00a0 3281-3283.<\/li>\n
  22. \u201cUrotropin azelate: a rather unwilling co-crystal.\u201d\u00a0<\/strong>M.\u00a0<\/strong>Bonin, T. R. Welberry, M. Hostettler, M. Gardon, H. Birkedal, G. Chapuis, P. Moeckli, C. A. Ogle, K. J. Schenk,\u00a0Acta Crystallographica, Section B: Structural Science<\/span>\u00a0 59(1),\u00a0 72-86 (2003).<\/li>\n
  23. \u201cRapid-Injection NMR Study of Iodo- and Cyano-Gilman Reagents with Cyclo-hexenone: Observation of p-Complexes and their rate of formation.\u201d\u00a0 S. H. Bertz, C. M. Carlin, D. A. Deadwyler, M. D. Murphy, C. A. Ogle, and P. H. Seagle,\u00a0J. Am. Chem. Soc<\/span>., 124, 13650-13651(2002).<\/li>\n
  24. Chloro(1,5-cyclooctadiene)(triphenylphosphine)-rhodium(I) Q. L. Horn, D. S. Jones, R. N. Evans, C. A. Ogle and T. Craig Masterman,\u00a0Acta Crystallographica Section E58<\/span>, m51-52 (2002).<\/li>\n
  25. \u201cPreparation of the Tomato Pinworm Pheromone, (E)-4-Tridecenyl Acetate, from Dihydropyran andn<\/em>-Octyllithium.\u201d J. P. Mitchener Jr.,\u00a0J. C. Thomas<\/em>\u00a0and C. A. Ogle,\u00a0Main Group Metal Chemistry<\/span>, 22, 435 (1999).<\/li>\n
  26. \u201cRe-evaluation of Organocuprate Reactivity.\u00a0 Logarithmic Reactivity Profiles for Iodo- vs. Cyano-Gilman Reagents in the Reactions of Organocuprates with 2-Cyclohexenone and Iodocyclohexane.\u201d S. H. Bertz, A. Chopra, M. Eriksson, C. A. Ogle,\u00a0Chemistry, A European Journal<\/span>.1999<\/strong>, 2680-92 (1999).<\/li>\n
  27. “Lithium Alkoxide Modifiers: Their Effect on the Rate of Polymerization and Propagation of Styrene by Butyllithium, in THF at -80\u00b0C.” C. A. Ogle, H. C. Johnson IV, X. L. Wang, C. M. Carlin, F. H. Strickler and B. Gordon III,\u00a0J. Poly. Science Part. A Polymer Chemistry<\/span>,\u00a037<\/strong>, 1157-68 (1999).<\/li>\n
  28. \u201cBenzyllithium: Preparation, Reactions and X-RAY Crystal Structure of Benzyllithium\u00b72THF\u201d\u00a0M. Hage<\/em>, C. A. Ogle, T. L. Rathman and J. L. Hubbard,\u00a0Main Group Met. Chem<\/span>.\u00a021<\/strong>, 777 (1998).<\/li>\n
  29. \u201cDirected Dilithiation of Diaryl Compounds: Preparation of Tricyclic Pharmaceuticals Based on the Dibenzoheteroazapine Skeleton.\u201d A. Chopra,\u00a0D. C. Dorton<\/em>\u00a0and C. A. Ogle,\u00a0Main Group Met. Chem.<\/span>,21<\/strong>, 25 (1998).<\/li>\n
  30. \u201cDirected Ortho Dilithiation of Diaryl Compounds: Facile Synthesis of Tricyclic Compounds Based on Heterocycles Fused to Two Benzene Rings.\u201d A. Chopra, D. C. Dorton<\/em>\u00a0and C. A. Ogle,\u00a0Main Group Met. Chem.<\/span>,\u00a020<\/strong>, 783 (1997).<\/li>\n
  31. \u201cA Novel Approach to Tricyclic Pharmaceuticals via Directed Dilithiation of Diaryl Compounds.\u201d\u00a0V. B. Birman<\/em>, A. Chopra and C. A. Ogle,\u00a0Tetrahedron Letters<\/span>, 37, 5073 (1996).<\/li>\n
  32. “The Effect of Lithium Aggregates in Anionic Polymerizations.” C. A. Ogle, H. C. Johnson IV, X. L. Wang, F. H. Strickler, D. Bucca and B. Gordon III,\u00a0Polymeric Materials Encyclopedia<\/span>, CRC Press, 1996.<\/li>\n
  33. \u201cThe Structure and Reactivity of Organolithium Reagents.\u201d C. A. Ogle\u00a0LithiumLink<\/span>, 1-18, Summer (1995).<\/li>\n
  34. “The Rate of Polymerization of Styrene in THF at -80\u00b0C by\u00a0n<\/em>-,\u00a0sec<\/em>– and\u00a0t<\/em>-Butyllithium.” C. A. Ogle, F. H. Strickler, D. Bucca, X. L. Wang and B. Gordon III,\u00a0Macromolecules<\/span>, 28, 5184 (1995).<\/li>\n
  35. “The Polymerization of Styrene by\u00a0n<\/em>-,\u00a0sec<\/em>– and\u00a0t<\/em>-Butyllithium, in THF.” C. A. Ogle, X. L. Wang, H. C. Johnson IV, F. H. Strickler and B. Gordon III,\u00a0Polym. Prep.<\/span>\u00a034(2), 336 (1993).<\/li>\n
  36. “The Reaction of\u00a0 Polystyryllithium with THF.” C. A. Ogle, F. H. Strickler and B. Gordon IIIMacromolecules<\/span>, 26, 5803 (1993).<\/li>\n
  37. “The Isolation, Characterization and Crystal Structure of [MeLiTHF]4.”\u00a0B. K. Huckabee<\/em>, C. A. Ogle, A. A. Pinkerton,\u00a0P. F. Sims<\/em>\u00a0and\u00a0S. D. Winslow<\/em>,\u00a0 H. C. Johnson IV\u00a0Organometallics<\/span>, 12, 1960 (1993).<\/strong><\/li>\n
  38. “n<\/em>-Caprylammonium Chloride: A Solid Membrane Model.” K. J.\u00a0 Schenk, C. A. Ogle, D. Schwarzenbach, G. C. Chapuis, J. C. Cornut and M. Rey-Lafon,\u00a0J. Phys. Chem.<\/span>, 96, 5530-6\u00a0 (1992).<\/li>\n
  39. “Lithium Alkoxide Modifiers: Their Effect on the Rate of Polymerization of Styrene by\u00a0n<\/em>-Butyllithium, in THF at -80\u00b0C.” C. A. Ogle, X. L. Wang, F. H. Strickler and B. Gordon III,\u00a0Polymer Prep<\/span>. 33(2), 190 (1992).<\/li>\n
  40. “Tris(2,4,6-Trimethoxyphenyl)Phosphine.\u00a0 Resolution of Space Group Ambiguity by Solid State NMR.”\u00a0 G. Nemeth, A. A. Pinkerton,\u00a0J. A. Stowe<\/em>\u00a0and C. A. Ogle,\u00a0Acta Cryst<\/span>., C48, 2200 (1992).<\/strong><\/li>\n
  41. “Preparation and Ring-Opening of Benzylic and Allylic Cyclopropyl Dianions.” C. A. Ogle,\u00a0K. C. Black<\/em>\u00a0and\u00a0P. F. Sims<\/em>,\u00a0J. Org. Chem<\/span>., 57, 3499 (1992).<\/strong><\/li>\n
  42. “Mechanistic Studies on the Base-Promoted Addition of Lithiopinacolonate to Several Aromatic Carbonyl Compounds in Nonhydroxylic Solvents.”\u00a0 C. A. Palmer, C. A. Ogle and E. M. Arnett,\u00a0J. Am. Chem. Soc<\/span>., 114, 5619 (1992).<\/li>\n
  43. “The Nature of the Living End of Polystyryllithium in the Presence of Lithium-t<\/em>-Butoxide: A Semi-Empirical Molecular Orbital Study.”\u00a0 H. C. Johnson IV and C. A. Ogle,\u00a0Polymer Prep.<\/span>, 33(1), 1178 (1992).<\/li>\n
  44. “Preparation and Ring Opening of Benzylic and Allylic Cyclopropyl Anions.”\u00a0P. F. Sims<\/em>,\u00a0K. C. Black<\/em>and C. A. Ogle,\u00a0CANCAS<\/span>, 37(1), 113 (1991).<\/li>\n
  45. “NMR Studies of Mixed Aggregation in Alkyllithium Compounds.” C. A. Ogle and\u00a0M. W. Wright<\/em>,CANCAS<\/span>, 37(1), 100 (1991).<\/li>\n
  46. “Benzoylated Polystyrene: A Nonvolatile Visual Indicator for the Drying of Ethers with IA Metals.”\u00a0 C. A. Ogle and B. Gordon III,\u00a0Polymer Prep<\/span>., 32(1), 84 (1991).<\/li>\n
  47. “Delocalized Carbanions in Synthesis.”\u00a0 C. E. Barry III; R. B. Bates; W. A. Beavers; F. A. Camou; B. Gordon III; H. F. Hsu; N. S. Mills; C. A. Ogle; T. J. Siahaan; et al.,\u00a0Synlett.<\/span>, 207-12 (1991).<\/li>\n
  48. “The Structure of Crystalline Trans-dichlorobis(triphenylphosphine) Rhodium(II), a Square Planar Rh(II) Monomer: Isolation of the Proposed Paramagnetic Impurity in Wilkinson’s Catalyst.” C. A. Ogle,\u00a0T. C. Masterman<\/em>\u00a0and J. L. Hubbard,\u00a0\u00a0J. Chem. Soc. Chem. Commun.<\/span>, 1733-4 (1990).<\/strong><\/li>\n
  49. “A Convenient One-Pot Method for the Hydroxymethylation of Grignard Reagents.” C. A. Ogle,\u00a0T. E. Wilson<\/em>\u00a0and\u00a0J. A. Stowe<\/em>,\u00a0Synthesis<\/span>, 495-6 (1990).<\/strong><\/li>\n
  50. “An Inexpensive Alternative to a Commercial Variable Transformer,” C. A. Ogle and C. E. Barnes,\u00a0J. Chem. Education<\/span>, 240, 67 (1990).<\/li>\n
  51. “RINMR Studies of\u00a0n<\/em>-Butyllithium and Styrene.”\u00a0 C. A. Ogle, D. Bucca and B. Gordon III,\u00a0Polymer Prep.<\/span>, 30(1), 135-6 (1989).<\/li>\n
  52. “A Vibrational and Structural Study of the Phase Transitions in the Layer Compound\u00a0n<\/em>-Decylammonium Chloride,” R. Cavangnat, G. C. Chapuis, J. C. Cornut,\u00a0A. Jokic<\/em>, C. A. Ogle, M. Rey-Lafon and K. J. Schenk,\u00a0J. Phy. Chem.<\/span>, 93, 5040-9 (1989).<\/li>\n
  53. “A Reinvestigation of the Metalation of Phenylcyclopropane: Does the Phenylcyclopropyl Anion Undergo Ring-Opening?” C. A. Ogle,\u00a0P. A. Riley<\/em>, J. J. Dorchak and J. L. Hubbard,\u00a0J. Org. Chem<\/span>., 53, 4409-12 (1988).<\/strong><\/li>\n
  54. “A Rapid Injection NMR Study of the Reactivity of Butyllithium Aggregates in Tetrahydrofuran,” J. F. McGarrity, C. A. Ogle, Z. Brich and H. R. Loosli,\u00a0J. Am. Chem. Soc<\/span>., 107, 1810 (1985).<\/li>\n
  55. “A High Field 1H NMR Study of the Aggregation and Complexation of\u00a0n<\/em>-Butyllithium in Tetrahydrofuran,” C. A. Ogle and J. F. McGarrity,\u00a0J. Am. Chem. Soc<\/span>., 107, 1805 (1985).<\/li>\n
  56. “Decomposition Rates, Synthesis and Spectral Properties of a Series of Alkyl Hyponitrites,”\u00a0 C. A. Ogle, S. W. Martin, M. P. Dziobak, M. W. Urban, G. D. Mendenhall,\u00a0J. Org. Chem.<\/span>, 48, 3728 (1983).<\/li>\n
  57. “1,4,7-Trithiacyclononane, a Novel Tridentate Thioether Ligand and The Structure of Its\u00a0 Nickel (II), Cobalt (II), and Copper (II)Complexes,”\u00a0 W. N. Setzer, C. A. Ogle, G. S. Wilson, R. S. Glass,\u00a0Inorg. Chem<\/span>., 22, 266 (1983).<\/li>\n
  58. “Laser Raman and Infrared Spectra, and X-ray Crystal Structure of trans Di-tert-butyl Hyponitrite,” C. A Ogle, K. A. VanderKooi, G. D. Mendenhall, V. Lorprayoon, and B. C. Cornilsen,\u00a0J. Am. Chem. Soc.<\/span>, 104, 5ll4 (1982).<\/li>\n
  59. “Arenes Disubstituted with Primary Alkyl Groups from Xylylene Dianions,”\u00a0 R. B. Bates and C. A. Ogle,\u00a0J. Org. Chem<\/span>., 47, 3949 (1982).<\/li>\n
  60. “Di- and Higher Delocalized Carbanions,” R. B. Bates, B. A. Hess Jr., C. A. Ogle, and L. J. Schaad,\u00a0J. Am. Chem. Soc.<\/span>, 103, 5052 (1981).<\/li>\n
  61. “Nonisothermal Kinetic Analysis of the Chemiluminescence from Tetramethyl-1,2-dioxetane,” G. D. Mendenhall, J. C. Tauscheck, and C. A. Ogle,\u00a0Int. J. Chem. Kinetics<\/span>, 13, 1217 (1981).<\/li>\n
  62. “The Use of Chemiluminescence in the Study of Paper Permanence,” G. B. Kelly, J. C. Williams, G. D. Mendenhall, and C. A. Ogle.\u00a0 In “Durability of Macromolecular Materials.”\u00a0 R. K. Eby Ed.; American Chemical Society: Washington, D.C., 1979.<\/li>\n
  63. “Low-Temperatur Chemiluminescence from cis-1,4-Polybutadiene, 1,2-Polybutadiene, and trans-Polypentenamer at Temperatures Near Ambient,” R. A. Nathan, G. D. Mendenhall, M. A. Birts, C. A. Ogle, and M. A. Golub.\u00a0 In “Stabilization and Degradation of Polymers.” D. L. Allara and W. L. Hawkins, Ed.; American Chemical Society: Washington, D.C., 1978.<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

    Steven H. Bertz, Richard A. Hardin, Michael D. Murphy, Craig A. Ogle, Joshua D. Richter and Andy A. Thomas \u201cMinimization of Organocuprate Complexity through Self-Organization: Remarkable Orientation Effect in Mixed Cuprate \u03c0-Complexes”,\u00a0Angewandte Chemie, International Edition (2012) 51(11) 2681-5. Steven H. Bertz, Richard A. Hardin, Michael D. Murphy, Craig A. Ogle, Joshua D. Richter, and Andy […]<\/p>\n","protected":false},"author":25,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"open","template":"page-left-sidebar.php","meta":{"jetpack_post_was_ever_published":false,"footnotes":""},"class_list":["post-37","page","type-page","status-publish","hentry"],"jetpack_shortlink":"https:\/\/wp.me\/P2WtrN-B","jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/pages.charlotte.edu\/craig-ogle\/wp-json\/wp\/v2\/pages\/37","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pages.charlotte.edu\/craig-ogle\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/pages.charlotte.edu\/craig-ogle\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/pages.charlotte.edu\/craig-ogle\/wp-json\/wp\/v2\/users\/25"}],"replies":[{"embeddable":true,"href":"https:\/\/pages.charlotte.edu\/craig-ogle\/wp-json\/wp\/v2\/comments?post=37"}],"version-history":[{"count":7,"href":"https:\/\/pages.charlotte.edu\/craig-ogle\/wp-json\/wp\/v2\/pages\/37\/revisions"}],"predecessor-version":[{"id":140,"href":"https:\/\/pages.charlotte.edu\/craig-ogle\/wp-json\/wp\/v2\/pages\/37\/revisions\/140"}],"wp:attachment":[{"href":"https:\/\/pages.charlotte.edu\/craig-ogle\/wp-json\/wp\/v2\/media?parent=37"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}