Chemical communications (Cambridge, England), 47(41), 11465-11467 (2011-09-29)
Sultones were subject to ring opening by nucleophilic attack with [(18)F]fluoride to afford easily purified (18)F-labelled hydrophilic sulfonated products in high yields. A two-step sequence including radiofluorination and coupling to lysine was then developed from a bis-sultone precursor as a
A rationale for the selection of occlusion to induce and elicit delayed contact hypersensitivity in the guinea pig. A prospective test.
E V Buehler
Current problems in dermatology, 14, 39-58 (1985-01-01)
Journal of medicinal chemistry, 52(6), 1582-1591 (2009-02-20)
We report the synthesis and antiviral activity of a new family of non-nucleoside antivirals, derived from the 4-keto-1,2-oxathiole-2,2-dioxide (beta-keto-gamma-sultone) heterocyclic system. Several 4- and 5-substituted-5H-1,2-oxathiole-2,2-dioxide derivatives were found to have a selective inhibitory activity against human cytomegalovirus (HCMV) and varicella
Single injection adjuvant test.
B F Goodwin et al.
Current problems in dermatology, 14, 201-207 (1985-01-01)
DNA adducts of lactones, sultones, acylating agents and acrylic compounds.
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