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Journal Abstract Search

151 related items for PubMed ID: 24254980

  • 1. Absolute configuration of oplopanone derivatives from Serphidium stenocephalum: ECD spectra of acyclic ketones with front-octant contributions.
    Shafiq N, Saleem M, Riaz N, Tousif MI, Jabbar A, Tareen RB, Pescitelli G.
    Chirality; 2014 Jan; 26(1):39-43. PubMed ID: 24254980
    [Abstract] [Full Text] [Related]

  • 2. Vibronic coupling dominates the electronic circular dichroism of the benzene chromophore ¹L(b) band.
    Pescitelli G, Barone V, Di Bari L, Rizzo A, Santoro F.
    J Org Chem; 2013 Aug 02; 78(15):7398-405. PubMed ID: 23834013
    [Abstract] [Full Text] [Related]

  • 3. The Assignment of the Absolute Configuration of Non-Cyclic Sesquiterpenes by Vibrational and Electronic Circular Dichroism: The Example of Chiliadenus lopadusanus Metabolites.
    Mazzeo G, Cimmino A, Longhi G, Masi M, Evidente A, Abbate S.
    Biomolecules; 2021 Dec 18; 11(12):. PubMed ID: 34944545
    [Abstract] [Full Text] [Related]

  • 4. Determination of the absolute configurations of natural products via density functional theory calculations of optical rotation, electronic circular dichroism, and vibrational circular dichroism: the cytotoxic sesquiterpene natural products quadrone, suberosenone, suberosanone, and suberosenol A acetate.
    Stephens PJ, McCann DM, Devlin FJ, Smith AB.
    J Nat Prod; 2006 Jul 18; 69(7):1055-64. PubMed ID: 16872144
    [Abstract] [Full Text] [Related]

  • 5. Determination of absolute configuration using concerted ab Initio DFT calculations of electronic circular dichroism and optical rotation: bicyclo[3.3.1]nonane diones.
    Stephens PJ, McCann DM, Butkus E, Stoncius S, Cheeseman JR, Frisch MJ.
    J Org Chem; 2004 Mar 19; 69(6):1948-58. PubMed ID: 15058939
    [Abstract] [Full Text] [Related]

  • 6. Study on the absolute configuration of levetiracetam via density functional theory calculations of electronic circular dichroism and optical rotatory dispersion.
    Li L, Si YK.
    J Pharm Biomed Anal; 2011 Nov 01; 56(3):465-70. PubMed ID: 21794998
    [Abstract] [Full Text] [Related]

  • 7. How and How Much Molecular Conformation Affects Electronic Circular Dichroism: The Case of 1,1-Diarylcarbinols.
    Padula D, Pescitelli G.
    Molecules; 2018 Jan 09; 23(1):. PubMed ID: 29315220
    [Abstract] [Full Text] [Related]

  • 8. Absolute configuration of lippifoliane and africanane derivatives.
    Cerda-García-Rojas CM, Coronel Adel C, de Lampasona ME, Catalán CA, Joseph-Nathan P.
    J Nat Prod; 2005 May 09; 68(5):659-65. PubMed ID: 15921405
    [Abstract] [Full Text] [Related]

  • 9. Three Sesquiterpenoid Dimers from Chloranthus japonicus: Absolute Configuration of Chlorahololide A and Related Compounds.
    Shi XW, Lu QQ, Pescitelli G, Ivšić T, Zhou JH, Gao JM.
    Chirality; 2016 Feb 09; 28(2):158-63. PubMed ID: 26708509
    [Abstract] [Full Text] [Related]

  • 10. Absolute configurations of phytotoxic inuloxins B and C based on experimental and computational analysis of chiroptical properties.
    Evidente M, Santoro E, Petrovic AG, Cimmino A, Koshoubu J, Evidente A, Berova N, Superchi S.
    Phytochemistry; 2016 Oct 09; 130():328-34. PubMed ID: 27498046
    [Abstract] [Full Text] [Related]

  • 11. Experimental and calculated CPL spectra and related spectroscopic data of camphor and other simple chiral bicyclic ketones.
    Longhi G, Castiglioni E, Abbate S, Lebon F, Lightner DA.
    Chirality; 2013 Oct 09; 25(10):589-99. PubMed ID: 23840012
    [Abstract] [Full Text] [Related]

  • 12. Chromane helicity rule--scope and challenges based on an ECD study of various trolox derivatives.
    Górecki M, Suszczyńska A, Woźnica M, Baj A, Wolniak M, Cyrański MK, Witkowski S, Frelek J.
    Org Biomol Chem; 2014 Apr 14; 12(14):2235-54. PubMed ID: 24569389
    [Abstract] [Full Text] [Related]

  • 13. To Avoid Chasing Incorrect Chemical Structures of Chiral Compounds: Raman Optical Activity and Vibrational Circular Dichroism Spectroscopies.
    Polavarapu PL, Covington CL, Raghavan V.
    Chemphyschem; 2017 Sep 20; 18(18):2459-2465. PubMed ID: 28700810
    [Abstract] [Full Text] [Related]

  • 14. Theoretical calculation of electronic circular dichroism of the rotationally restricted 3,8''-biflavonoid morelloflavone.
    Ding Y, Li XC, Ferreira D.
    J Org Chem; 2007 Nov 23; 72(24):9010-7. PubMed ID: 17958369
    [Abstract] [Full Text] [Related]

  • 15. Structural and stereochemical studies of a tetralin norsesquiterpenoid from Ligularia kangtingensis.
    Xie G, Tian J, Kövér KE, Mándi A, Kurtán T.
    Chirality; 2014 Sep 23; 26(9):574-9. PubMed ID: 24830355
    [Abstract] [Full Text] [Related]

  • 16. Determination of the absolute configurations of natural products via density functional theory calculations of vibrational circular dichroism, electronic circular dichroism, and optical rotation: the iridoids plumericin and isoplumericin.
    Stephens PJ, Pan JJ, Devlin FJ, Krohn K, Kurtán T.
    J Org Chem; 2007 Apr 27; 72(9):3521-36. PubMed ID: 17388636
    [Abstract] [Full Text] [Related]

  • 17. Enantiomeric discorhabdin alkaloids and establishment of their absolute configurations using theoretical calculations of electronic circular dichroism spectra.
    Grkovic T, Ding Y, Li XC, Webb VL, Ferreira D, Copp BR.
    J Org Chem; 2008 Nov 21; 73(22):9133-6. PubMed ID: 18855481
    [Abstract] [Full Text] [Related]

  • 18. Good Computational Practice in the Assignment of Absolute Configurations by TDDFT Calculations of ECD Spectra.
    Pescitelli G, Bruhn T.
    Chirality; 2016 Jun 21; 28(6):466-74. PubMed ID: 27098594
    [Abstract] [Full Text] [Related]

  • 19. Revising the absolute configurations of coatlines via density functional theory calculations of electronic circular dichroism spectra.
    Genta-Jouve G, Weinberg L, Cocandeau V, Maestro Y, Thomas OP, Holderith S.
    Chirality; 2013 Mar 21; 25(3):180-4. PubMed ID: 23280651
    [Abstract] [Full Text] [Related]

  • 20. Ring-expanded bicyclic β-lactams: a structure-chiroptical properties relationship investigation by experiment and calculations.
    Woźnica M, Butkiewicz A, Grzywacz A, Kowalska P, Masnyk M, Michalak K, Luboradzki R, Furche F, Kruse H, Grimme S, Frelek J.
    J Org Chem; 2011 May 06; 76(9):3306-19. PubMed ID: 21438506
    [Abstract] [Full Text] [Related]

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