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Chelation as a Driving Force in Organic Reactions. IV.1 Synthesis of α-Nitro Acids by Control of the Carboxylation-Decarboxylation Equilibrium 2
National licenceAmerican Chemical Society | 1963| -
CHELATION AS A DRIVING FORCE IN SYNTHESIS. A NEW ROUTE TO α-NITRO ACIDS AND α-AMINO ACIDS
National licenceAmerican Chemical Society | 1959| -
Identification of an A2a Adenosine Receptor Domain Specifically Responsible for Mediating Short-Term Desensitization †
American Chemical Society | 1997| -
Phosphoric-Carbonic Anhydrides.1 The Hydrolysis of Dibenzyl p-Nitrocarbobenzoxy Phosphate
National licenceAmerican Chemical Society | 1965| -
Patterns of Trade in Ethnic Enclaves: A Study of Arab and Hispanic Small Businesses
Taylor & Francis Verlag | 2003| -
Toxicity of Volcanic-Ash Leachate to a Blue-Green Alga. Results Of A Preliminary Bioassay Experiment
National licenceAmerican Chemical Society | 1981| -
The Nitrogen Compounds in Petroleum Distillates. XXVII. Isolation and Identification of 2,3-Dimethyl-6-isopropyl-pyridine from California Petroleum
National licenceAmerican Chemical Society | 1950| -
NMR assignment of leucocin A, a bacteriocin from Leuconostoc gelidum, supported by a stable isotope-labeling technique for peptides and proteins
National licenceAmerican Chemical Society | 1992| -
Nitrogen-15- and carbon-13-labeled media from Anabaena sp. for universal isotopic labeling of bacteriocins: NMR resonance assignments of leucocin A from Leuconostoc gelidum and nisin A from Lactococcus lactis
National licenceAmerican Chemical Society | 1993| -
Inhibiting the Hexosamine Biosynthetic Pathway Lowers O‑GlcNAcylation Levels and Sensitizes Cancer to Environmental Stress
American Chemical Society | 2020| -
Size Limitations for the Formation of Ordered Striped Nanoparticles
American Chemical Society | 2008|
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