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Selective Cycloaddition Reactions of Sulfo-Biginelli Derived 1,2,6-Thiadiazines

open access: yes
Modified sulfo-Biginelli conditions were developed to access dihydro-1,2,6-thiadiazines that were further functionalized and oxidized to 1,2,6-thiadiazines. These electron-deficient heterocyclic building blocks were subjected to regio- and stereoselective [4+2] and [3+2] cycloadditions with an electron-rich methylene cyclopropane, non-stabilized ...
Clare Hill, Michael Sambor, Peter Wipf
openaire   +1 more source

1,2,6-Thiadiazinones as Novel Narrow Spectrum Calcium/Calmodulin-Dependent Protein Kinase Kinase 2 (CaMKK2) Inhibitors. [PDF]

open access: yesMolecules, 2018
Asquith CRM   +11 more
europepmc   +1 more source

Looking for Novel Capsid Protein Multimerization Inhibitors of Feline Immunodeficiency Virus. [PDF]

open access: yesPharmaceuticals (Basel), 2018
Sierra N   +5 more
europepmc   +1 more source

Dibenzo[1,2,5]thiadiazepines are non-competitive GABAA receptor antagonists. [PDF]

open access: yesMolecules, 2013
Ramírez-Martínez JF   +8 more
europepmc   +1 more source

3,5-Dichloro-4H-1,2,6-thiadiazin-4-one [PDF]

open access: yesActa Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1978
openaire   +2 more sources

Conformationally rigid histone deacetylase inhibitors correct DF508-CFTR protein function [PDF]

open access: yes, 2011
Balch, William E.   +7 more
core  

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