Relevant bibliographies by topics / Duke University, Durham, N.C

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Academic literature on the topic 'Duke University, Durham, N.C'

Author: Grafiati
Published: 4 June 2021
Last updated: 17 February 2022

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Journal articles on the topic "Duke University, Durham, N.C"

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Barner-Barry, Carol. "Leaders Under Stress: A Psychophysiological Analysis of International CrisesThomas C. Wiegele, Gordon Hilton, Kent Layne Oots, and Susan V. Kisiel Durham, N. C.: Duke University Press, 1985." Politics and the Life Sciences 5, no. 1 (August 1986): 170. http://dx.doi.org/10.1017/s073093840000191x.

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McKelvey, James. "Richard P. Heitzenrater, editor. Diary of an Oxford Methodist: Benjamin Ingham, 1733-1734. Durham, N. C.: Duke University Press. 1985. Pp. xvi, 304. $37.50." Albion 18, no. 3 (1986): 499–500. http://dx.doi.org/10.2307/4050000.

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Gervais, Pierre. "Martin Bruegel, Farm, Shop, Landing : the Rise of a Market Society in the Hudson Valley, 1780-1860, Durham (N. C.), Duke University Press, 2000." Revue d’histoire moderne et contemporaine 51-2, no. 2 (2004): 227. http://dx.doi.org/10.3917/rhmc.512.0227.

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4

Lawrence, Christopher. "Kathleen Wellman, La Mettrie: medicine, philosophy, and Enlightment, Durham, N. C., and London, Duke University Press, 1992, pp. xiv, 342, £29.92 (0-8223-1204-2)." Medical History 37, no. 1 (January 1993): 101–2. http://dx.doi.org/10.1017/s0025727300057835.

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5

Levi, Heather. "Fighting for Recognition: Identity, Masculinity and the Act of Violence in Professional Wrestling. R. Tyson Smith. Durham, N. C.: Duke University Press, 2014. Pp. xvi+220." American Journal of Sociology 121, no. 4 (January 2016): 1315–17. http://dx.doi.org/10.1086/683633.

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6

Haakonssen, Knud. "Richard F. TeichgraeberIII. “Free Trade” and Moral Philosophy: Rethinking the Sources of Adam Smith's “Wealth of Nations.”Durham, N. C.: Duke University Press. 1986. Pp. xviii, 211. $35.00." Albion 19, no. 3 (1987): 441–43. http://dx.doi.org/10.2307/4050494.

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7

McKeown, Adam. "Reimagining the American Pacific: From South Pacific to Bamboo Ridge and Beyond. By Rob Wilson. Durham, N. C.: Duke University Press, 2000. xix, 295 pp. $54.95 (cloth); $19.95 (paper)." Journal of Asian Studies 60, no. 2 (May 2001): 517–18. http://dx.doi.org/10.2307/2659716.

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Postlethwaite, Diana. "Alan Rauch. Useful Knowledge: The Victorians, Morality, and the March of Intellect. Durham, N. C.: Duke University Press. 2001. Pp. x, 293. $19.95 paper. ISBN 0-8223-2668-x." Albion 34, no. 4 (2002): 671–72. http://dx.doi.org/10.1017/s0095139000068800.

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9

Wilder, William D. "Race and the Education of Desire: Foucault's History of Sexuality and the Colonial Order of Things. By Ann Laura Stoler. Durham, N. C: Duke University Press, 1995. xiv, 237 pp. $49.95 (cloth); $15.95 (paper)." Journal of Asian Studies 55, no. 4 (November 1996): 1086–87. http://dx.doi.org/10.2307/2646611.

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10

Misse, Michel. "Hard Times in the Marvelous City: From Dictatorship to Democracy in the Favelas of Rio de Janeiro. By Bryan McCann. Durham, N. C.: Duke University Press, 2014. Pp. xii+249. $89.95 (cloth): $24.95 (paper)." American Journal of Sociology 120, no. 4 (January 2015): 1267–69. http://dx.doi.org/10.1086/679220.

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Book chapters on the topic "Duke University, Durham, N.C"

1

Lambert, Tristan H. "New Methods for C–N Ring Construction." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0055.

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The reduction of pyridines offers an attractive approach to piperidine synthesis, and now Toshimichi Ohmura and Michinori Suginome of Kyoto University have developed (J. Am. Chem. Soc. 2012, 134, 3699) a rhodium-catalyzed hydroboration of pyridines, including the reaction of 1 to produce 3. Timothy J. Donohoe at the University of Oxford has found (Org. Lett. 2011, 13, 2074) that pyridinium silanes 4 undergo intramolecular hydride transfer by treatment with TBAF to produce dihydropyridones (e.g., 5) with good diastereoselectivity. Enantioselective amination of allylic alcohols has proven challenging, but Ross A. Widenhoefer at Duke University has reported (Angew. Chem. Int. Ed. 2012, 51, 1405) that a chiral gold catalyst can effect such intramolecular cyclizations with good enantioselectivity, as in the synthesis of 7 from 6. Alternatively, Masato Kitamura at Nagoya University has developed (Org. Lett. 2012, 14, 608) a ruthenium catalyst that operates at as low as 0.05 mol% loading for the conversion of substrates such as 8 to 9. Efforts to replace transition metal catalysts with alkaline earth metal-based alternatives have been gaining increasing attention, and Kai C. Hultzsch at Rutgers University has found (Angew. Chem. Int. Ed. 2012, 51, 394) that the magnesium complex 12 is capable of catalyzing intramolecular hydroamination (e.g., 10 to 11) with high enantioselectivity. Meanwhile, a stereoselective Wacker-type oxidation of tert-butanesulfinamides such as 13 to produce pyrrolidine derivatives 14 has been disclosed (Org. Lett. 2012, 14, 1242) by Shannon S. Stahl at the University of Wisconsin at Madison. Though highly desirable, Heck reactions have rarely proven feasible with alkyl halides due to competitive β-hydride elimination of the alkyl palladium intermediates. Sherry R. Chemler at the State University of New York at Buffalo has demonstrated (J. Am. Chem. Soc. 2012, 134, 2020) a copper-catalyzed enantioselective amination Heck-type cascade (e.g., 15 and 16 to 17) that is thought to proceed via radical intermediates. David L. Van Vranken at the University of California at Irvine has reported (Org. Lett. 2012, 14, 3233) the carbenylative amination of N-tosylhydrazones, which proceeds through η3-allyl Pd intermediates constructed via carbene insertion. This chemistry was applied to the two-step synthesis of caulophyllumine B from vinyl iodide 18 and N-tosylhydrazone 19.
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2

Taber, Douglass F. "C-N Ring Construction: The Synthesis of Decursivine by Mascal and by Jia." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0056.

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Barry M. Trost and Justin Du Bois of Stanford University described (Org. Lett. 2011, 13, 3336) the cyclization of 1 to the activated aziridine 2. Liming Zhang of the University of California, Santa Barbara, rearranged (Angew. Chem. Int. Ed. 2011, 50, 3236) the propergylic amine 3 to the azetidinone 4 by N-H insertion of an intermediate Au carbene. Xiao Zheng and Pei-Qiang Huang of Xiamen University effected (J. Org. Chem. 2011, 76, 4952) reductive coupling of 6 with 7 to deliver the ester 8 . Eiji Tayama of Niigata University found (Tetrahedron Lett. 2011, 52, 1819) that 9 could be alkenylated with 10 with substantial retention of absolute configuration. Duncan J. Wardrop of the University of Illinois at Chicago, en route to a synthesis of (-)-swainsonine, observed (Org. Lett. 2011 , 13, 2376) high diastereocontrol in the cyclization of 12 to 13. Iain Coldham of the University of Sheffield also observed (J. Org. Chem. 2011, 76, 2360) substantial diastereoselection in the cyclization of 14 to 15. Robert E. Gawley of the University of Arkansas established (Org. Lett. 2011, 13, 394) that exposure of metalated 16 to just 5 mol % of a chiral ligand was sufficient to enable enantioselective coupling, to deliver 17. Christian Nadeau of Merck Frosst effected (J. Am. Chem. Soc. 2011, 133, 2878) enantioselective addition to the pyridinium salt 19 to give 20. Jiyong Hong of Duke University observed (Org. Lett. 2011, 13, 796) that enantiomerically pure 21 cyclized to the cis diastereomer of 22. With the Hayashi catalyst, cyclization could be driven toward the trans diastereomer, 22, enabling the synthesis of (+)-myrtine. Dawei Ma of the Shanghai Institute of Organic Chemistry found (Org. Lett. 2011, 13, 1602) that the Hayashi catalyst also directed the relative and absolute outcome in the addition of 24 to 23 , to give the piperidine 25. Donn G. Wishka of Pfizer/Groton devised (J. Org. Chem. 2011, 76, 1937) a practical route to the cis-substituted azepane 27, by Beckmann rearrangement of the enantiomerically pure 26 followed by reduction and oxidative cleavage.
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