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Determination of Zinc Oxide in Pharmaceutical Preparations by EDTA Titration: A Practical Class for a Quantitative Analysis Course
American Chemical Society | 2020| -
Dihydroxyacetone Production: From Glycerol Catalytic Oxidation with Commercial Catalysts to Chromatographic Separation
American Chemical Society | 2021| -
A simple procedure for stereospecific vicinal dicarboxylation of olefins
National licenceAmerican Chemical Society | 1985| -
Pentacyanoferrate(II) complexes of pyrimidine and quinoxaline
National licenceAmerican Chemical Society | 1983| -
3D Transition Metal Ordering and Rietveld Stacking Fault Quantification in the New Oxychalcogenides La2O2Cu2–4x Cd2x Se2
American Chemical Society | 2016| -
An approach to the bakkanes. A short, stereocontrolled total synthesis of (.+-.)-bakkenolide A
National licenceAmerican Chemical Society | 1985| -
Stability of an Al-Fumarate MOF and Its Potential for CO2 Capture from Wet Stream
American Chemical Society | 2016| -
Multinuclear Solid-State NMR Investigation of Hexaniobate and Hexatantalate Compounds
American Chemical Society | 2016| -
Click Chemistry Approach to Assembly Proline Mimetic Libraries Containing 1,4-Substituted 1,2,3-Triazoles
American Chemical Society | 2008| -
Pulsed EPR and Ab Initio Calculation on [Ni(CN)4]3- in NaCl and KCl Host Lattices
American Chemical Society | 2001| -
First-Principles Calculation of NMR Parameters Using the Gauge Including Projector Augmented Wave Method: A Chemist’s Point of View
American Chemical Society | 2012| -
Quantitative Mass Spectrometry Analysis of Intact Hemoglobin A2 by Precursor Ion Isolation and Detection
American Chemical Society | 2013| -
Lycopene and β-Carotene Extraction from Tomato Processing Waste Using Supercritical CO2
American Chemical Society | 2003| -
Mechanism of Palladium(II)-Mediated Uncaging Reactions of Propargylic Substrates
American Chemical Society | 2019| -
First Comprehensive Bakkane Approach: Stereoselective and Efficient Dichloroketene-Based Total Syntheses of (±)- and (−)-9-Acetoxyfukinanolide, (±)- and (+)-Bakkenolide A, (−)-Bakkenolides III, B, C, H, L, V, and X, (±)- and (−)-Homogynolide A, (±)-Homogynolide B, and (±)-Palmosalide C
American Chemical Society | 2002|
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