71924-62-4Relevant articles and documents
Optically active fluorinated vasoconstrictors, methods for making them, and anesthetic formulations comprising them
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Page/Page column 4; 7-8; Sheet 4; Sheet 6, (2010/02/05)
(R)-6F-phenylephrine, essentially free of (S)-6F-phenylephrine, and an anesthetic formulation comprising (R)-6F-epinephrin or (R)-6F-phenylephrine and having improved stability compared to formulations containing their non-fluorinated analog, are disclosed. Further disclosed is a method of providing vasoconstriction in a mammal by administering the anesthetic formulation. The anesthetic composition can include an anesthetic, an (R)-chiral compound having the structure: wherein R1, R2, and R4 are independently selected from —H or —F, at least one of R1, R2, and R4 is —F, and R3 is selected from —OH, —H or —F, or a pharmaceutically acceptable salt or ester thereof, said vasoconstrictor being essentially free of the (S)-chiral form. Also, a method of chiral addition of cyanide to a ring-fluorinated phenaldehyde, employing an almond hydroxynitrile lyase enzyme, provided in the form of a reversibly soluble polymer conjugate ((R)-Finezyme?-H series biocatalysts) is disclosed. Several such biocatalysts are disclosed.
FLUORINATION OF SUBSTITUTED VERATROLES VIA REGIOSELECTIVE MERCURATION
Luxen, A.,Barrio, J.R.
, p. 1501 - 1504 (2007/10/02)
A regioselective aromatic ring fluorination of substituted veratroles was achieved via a mercuration-fluorodemercuration reaction.
