BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 32142193)

  • 1. The enduring legacy of Koji Nakanishi's research on natural products and bioorganic chemistry. Part 2. Inception and establishment of the ECD exciton chirality method in 1960s to 1970s: A marvel of Nakanishi's Japanese team.
    Harada N
    Chirality; 2020 May; 32(5):535-546. PubMed ID: 32142193
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The enduring legacy of Koji Nakanishi's research on bioorganic chemistry and natural products. Part 1: Isolation, structure determination and mode of action.
    Ellestad G; Zask A; Berova N
    Chirality; 2020 May; 32(5):632-651. PubMed ID: 32157754
    [TBL] [Abstract][Full Text] [Related]  

  • 3. ECD exciton chirality method today: a modern tool for determining absolute configurations.
    Pescitelli G
    Chirality; 2022 Feb; 34(2):333-363. PubMed ID: 34791704
    [TBL] [Abstract][Full Text] [Related]  

  • 4. For a Correct Application of the CD Exciton Chirality Method: The Case of Laucysteinamide A.
    Pescitelli G
    Mar Drugs; 2018 Oct; 16(10):. PubMed ID: 30332852
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chiral Molecular Science: How were the absolute configurations of chiral molecules determined? "Experimental results and theories".
    Harada N
    Chirality; 2017 Dec; 29(12):774-797. PubMed ID: 28981959
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exciton coupling between enones: Quassinoids revisited.
    Pescitelli G; Di Bari L
    Chirality; 2017 Sep; 29(9):476-485. PubMed ID: 28635069
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Assignment of absolute stereostructures through quantum mechanics electronic and vibrational circular dichroism calculations.
    Dai P; Jiang N; Tan RX
    J Asian Nat Prod Res; 2016; 18(1):72-91. PubMed ID: 26880597
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Axially chiral BODIPY DYEmers: an apparent exception to the exciton chirality rule.
    Bruhn T; Pescitelli G; Jurinovich S; Schaumlöffel A; Witterauf F; Ahrens J; Bröring M; Bringmann G
    Angew Chem Int Ed Engl; 2014 Dec; 53(52):14592-5. PubMed ID: 25354119
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis, molecular structure, and chiroptical properties of dibenzylidene derivatives of bicyclo[3.3.1]nonane and brexane.
    Stončius S; Neniškis A; Loganathan N; Wendt OF
    Chirality; 2015 Oct; 27(10):728-37. PubMed ID: 26415852
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The online assignment of the absolute configuration of natural products: HPLC-CD in combination with quantum chemical CD calculations.
    Bringmann G; Gulder TA; Reichert M; Gulder T
    Chirality; 2008 May; 20(5):628-42. PubMed ID: 18383126
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Determination of the absolute configurations at stereogenic centers in the presence of axial chirality.
    Polavarapu PL; Jeirath N; Kurtán T; Pescitelli G; Krohn K
    Chirality; 2009; 21 Suppl 1():E202-7. PubMed ID: 19899152
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Absolute configuration of chiral [2.2]paracyclophanes with intramolecular charge-transfer interaction. Failure of the exciton chirality method and use of the sector rule applied to the cotton effect of the CT transition.
    Furo T; Mori T; Wada T; Inoue Y
    J Am Chem Soc; 2005 Jun; 127(23):8242-3. PubMed ID: 15941231
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exciton chirality method in vibrational circular dichroism.
    Taniguchi T; Monde K
    J Am Chem Soc; 2012 Feb; 134(8):3695-8. PubMed ID: 22299596
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Point-to-Axial Chirality Transmission: A Highly Sensitive Triaryl Chirality Probe for Stereochemical Assignments of Amines.
    Mądry T; Czapik A; Kwit M
    J Org Chem; 2020 Aug; 85(16):10413-10431. PubMed ID: 32806087
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chiral sulfinates studied by optical rotation, ECD and VCD: the absolute configuration of a cruciferous phytoalexin brassicanal C.
    Taniguchi T; Monde K; Nakanishi K; Berova N
    Org Biomol Chem; 2008 Dec; 6(23):4399-405. PubMed ID: 19005600
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A CD exciton chirality method for determination of the absolute configuration of threo-beta-aryl-beta-hydroxy-alpha-amino acid derivatives.
    Lo LC; Yang CT; Tsai CS
    J Org Chem; 2002 Feb; 67(4):1368-71. PubMed ID: 11846688
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Determination of absolute configurations by X-ray crystallography and 1H NMR anisotropy.
    Harada N
    Chirality; 2008 May; 20(5):691-723. PubMed ID: 17935143
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Revision of the Absolute Configuration of Preussilides A-F Established by the Exciton Chirality Method.
    Pescitelli G; Di Bari L
    J Nat Prod; 2017 Oct; 80(10):2855-2859. PubMed ID: 29039947
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CD exciton chirality method for determination of the absolute configuration of beta-hydroxy-alpha-amino acid derivatives.
    Lo LC; Chen JY; Yang CT; Gu DS
    Chirality; 2001 May; 13(5):266-71. PubMed ID: 11317348
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evaluation of absolute configuration of naphthylphenyl-substituted oligosilanes by CD exciton chirality method.
    Oh HS; Imae I; Kawakami Y
    Chirality; 2003 Mar; 15(3):231-7. PubMed ID: 12582989
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.