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Curtis Haltiwanger

Showing results (1-10 of 14) with videos related to

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Journal of the American Chemical Society|June 9, 2018
Correction to "Synthesis and Crystal Structure of an Enantiomerically Pure, Internally Coordinated Alkylchloroborane. The Boron-Centered Anomeric Affect"Christopher S Shiner, Charles M Garner, R Curtis Haltiwanger
Journal of Pharmaceutical Sciences|October 4, 2005
Solid state characterization of mometasone furoate anhydrous and monohydrate formsXiaoming Sean Chen, Matthew Carillo, R Curtis Haltiwanger, et al.
Acta Crystallographica. Section C, Structural Chemistry|June 20, 2024
Preferential crystallization of (±)-pinenyllithium·TMEDAAlexander N Erickson, Curtis Haltiwanger, Masoumeh Rahim, et al.
Inorganic Chemistry|October 28, 2003
The first coordination complexes of selenones: a structural comparison with complexes of sulfonesEvgeny V Dikarev, Renee Y Becker, Eric Block, et al.
Inorganic Chemistry|February 28, 2006
Synthesis, structural and spectroscopic characterization, catalytic properties, and thermal transformations of new cyclic di- and trisiloxanediolato tantalum complexesRamesh N Kapoor, Francisco Cervantes-Lee, Charles F Campana, et al.
Bioorganic & Medicinal Chemistry Letters|August 6, 2002
Design and synthesis of conformationally restricted eight-Membered ring diketones as potential serine protease inhibitorsNeil D Pearson, Drake S Eggleston, R Curtis Haltiwanger, et al.
European Journal of Medicinal Chemistry|April 2, 2015
3,4-Diaza-bicyclo[4.1.0]hept-4-en-2-one phenoxypropylamine analogs of irdabisant (CEP-26401) as potent histamine-3 receptor inverse agonists with robust wake-promoting activityRobert L Hudkins, Nadine C Becknell, Jacquelyn A Lyons, et al.
Journal of Pharmaceutical Sciences|January 25, 2005
Structural analysis of polymorphism and solvation in tranilastFrederick G Vogt, Dawn E Cohen, Joshua D Bowman, et al.
Journal of Medicinal Chemistry|December 17, 2011
Design, synthesis, and anaplastic lymphoma kinase (ALK) inhibitory activity for a novel series of 2,4,8,22-tetraazatetracyclo[14.3.1.1³,⁷.1⁹,¹³]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene macrocyclesHenry J Breslin, Brandon M Lane, Gregory R Ott, et al.
Bioorganic & Medicinal Chemistry Letters|February 1, 2012
4-phenoxypiperidine pyridazin-3-one histamine H(3) receptor inverse agonists demonstrating potent and robust wake promoting activityRobert L Hudkins, Allison L Zulli, Reddeppa reddy Dandu, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Journal of the American Chemical Society|June 9, 2018
Correction to "Synthesis and Crystal Structure of an Enantiomerically Pure, Internally Coordinated Alkylchloroborane. The Boron-Centered Anomeric Affect"Christopher S Shiner, Charles M Garner, R Curtis Haltiwanger
Journal of Pharmaceutical Sciences|October 4, 2005
Solid state characterization of mometasone furoate anhydrous and monohydrate formsXiaoming Sean Chen, Matthew Carillo, R Curtis Haltiwanger, et al.
Acta Crystallographica. Section C, Structural Chemistry|June 20, 2024
Preferential crystallization of (±)-pinenyllithium·TMEDAAlexander N Erickson, Curtis Haltiwanger, Masoumeh Rahim, et al.
Inorganic Chemistry|October 28, 2003
The first coordination complexes of selenones: a structural comparison with complexes of sulfonesEvgeny V Dikarev, Renee Y Becker, Eric Block, et al.
Inorganic Chemistry|February 28, 2006
Synthesis, structural and spectroscopic characterization, catalytic properties, and thermal transformations of new cyclic di- and trisiloxanediolato tantalum complexesRamesh N Kapoor, Francisco Cervantes-Lee, Charles F Campana, et al.
Bioorganic & Medicinal Chemistry Letters|August 6, 2002
Design and synthesis of conformationally restricted eight-Membered ring diketones as potential serine protease inhibitorsNeil D Pearson, Drake S Eggleston, R Curtis Haltiwanger, et al.
European Journal of Medicinal Chemistry|April 2, 2015
3,4-Diaza-bicyclo[4.1.0]hept-4-en-2-one phenoxypropylamine analogs of irdabisant (CEP-26401) as potent histamine-3 receptor inverse agonists with robust wake-promoting activityRobert L Hudkins, Nadine C Becknell, Jacquelyn A Lyons, et al.
Journal of Pharmaceutical Sciences|January 25, 2005
Structural analysis of polymorphism and solvation in tranilastFrederick G Vogt, Dawn E Cohen, Joshua D Bowman, et al.
Journal of Medicinal Chemistry|December 17, 2011
Design, synthesis, and anaplastic lymphoma kinase (ALK) inhibitory activity for a novel series of 2,4,8,22-tetraazatetracyclo[14.3.1.1³,⁷.1⁹,¹³]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene macrocyclesHenry J Breslin, Brandon M Lane, Gregory R Ott, et al.
Bioorganic & Medicinal Chemistry Letters|February 1, 2012
4-phenoxypiperidine pyridazin-3-one histamine H(3) receptor inverse agonists demonstrating potent and robust wake promoting activityRobert L Hudkins, Allison L Zulli, Reddeppa reddy Dandu, et al.
Pageof 2