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51. 13C NMR studies of wheat germ agglutinin interactions with N-acetylglucosamine at a magnetically oriented bilayer surface

52. Pd-catalyzed cycloisomerization to 1,2-dialkylidenecycloalkanes. 2. Alternative catalyst system

55. Stereochemical definition of the natural product (6R,10R,13R, 14R,16R,17R,19S,20S,21R,24S,25S,28S,30S,32R,33R,34R,36S,37S,39R)‐azaspiracid‐3 by total synthesis and comparative analyses

56. Protocol/guidelines for 800 MHz NMR Metabolomics, University of Oslo, version VII

58. SHSQC and SHMBC ALW.pdf

59. Nuclear Magnetic Resonance Spectroscopy to Identify Metabolite Biomarkers of Nonresponsiveness to Targeted Therapy in Glioblastoma Tumor Stem Cells

60. Characterization of Inulin-Type Fructan from Platycodon grandiflorus and Study on Its Prebiotic and Immunomodulating Activity

62. Total synthesis of (6R,10R,13R,14R,16R,17R,19S,20R,21R,24S, 25S,28S,30S,32R,33R,34R,36S,37S,39R)-azaspiracid-3 reveals non-identity with the natural product

65. Structure Elucidation, Relative LC–MS Response and In Vitro Toxicity of Azaspiracids 7–10 Isolated from Mussels (Mytilus edulis)

66. Quantification of Fatty Acids and their Regioisomeric Distribution in Triacylglycerols from Porcine and Bovine Sources Using 13C NMR Spectroscopy.

67. Evidence that Listeria innocua modulates its membrane’s stored curvature elastic stress, but not fluidity, through the cell cycle

68. Searching for a UV-filter in the eyes of high flying birds

71. Total Synthesis of (6 R ,10 R ,13 R ,14 R ,16 R ,17 R ,19 S ,20 R ,21 R ,24 S , 25 S ,28 S ,30 S ,32 R ,33 R ,34 R ,36 S ,37 S ,39 R )‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product

72. Stereochemical Definition of the Natural Product (6 R ,10 R ,13 R , 14 R ,16 R ,17 R ,19 S ,20 S ,21 R ,24 S ,25 S ,28 S ,30 S ,32 R ,33 R ,34 R ,36 S ,37 S ,39 R )‐Azaspiracid‐3 by Total Synthesis and Comparative Analyses

73. Stereochemical Definition of the Natural Product (6 R ,10 R ,13 R , 14 R ,16 R ,17 R ,19 S ,20 S ,21 R ,24 S ,25 S ,28 S ,30 S ,32 R ,33 R ,34 R ,36 S ,37 S ,39 R )‐Azaspiracid‐3 by Total Synthesis and Comparative Analyses

74. Total Synthesis of (6 R ,10 R ,13 R ,14 R ,16 R ,17 R ,19 S ,20 R ,21 R ,24 S , 25 S ,28 S ,30 S ,32 R ,33 R ,34 R ,36 S ,37 S ,39 R )‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product

75. Erratum to “The common lavender (Lavandula angustifolia Mill.) pectic polysaccharides modulate phagocytic leukocytes and intestinal Peyer’s patch cells” [Carbohydr. Polym. 174 (2017) 948–959]

76. Tilia tomentosa pectins exhibit dual mode of action on phagocytes as β-glucuronic acid monomers are abundant in their rhamnogalacturonans I

80. The common lavender (Lavandula angustifolia Mill.) pectic polysaccharides modulate phagocytic leukocytes and intestinal Peyer’s patch cells

83. Identification of a Novel Series of Benzohopanes and Their Geochemical Significance

84. Identification of a Novel Series of Benzohopanes and Their Geochemical Significance

85. Identification of a Novel Series of Benzohopanes and Their Geochemical Significance

86. Isolation, structural elucidation, relative LC-MS response, and in vitro toxicity of novel azaspiracids from azadinium spinosum

92. Total Synthesis of (6<italic>R</italic>,10<italic>R</italic>,13<italic>R</italic>,14<italic>R</italic>,16<italic>R</italic>,17<italic>R</italic>,19<italic>S</italic>,20<italic>R</italic>,21<italic>R</italic>,24<italic>S</italic>, 25<italic>S</italic>,28<italic>S</italic>,30<italic>S</italic>,32<italic>R</italic>,33<italic>R</italic>,34<italic>R</italic>,36<italic>S</italic>,37<italic>S</italic>,39<italic>R</italic>)‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product

95. Isolation, Structure Elucidation, Relative LC-MS Response, and in Vitro Toxicity of Azaspiracids from the Dinoflagellate Azadinium spinosum

96. Compound 'J' in Late Cretaceous/Tertiary terrigenous oils revisited: Structure elucidation of a rearranged oleanane coeluting on GC with 18 beta(H)-oleanane

100. Isolation, Structure Elucidation, Relative LC-MS Response, and in Vitro Toxicity of Azaspiracids from the Dinoflagellate Azadinium spinosum

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