103438-92-2Relevant articles and documents
Syntheses of 6-fluoro-meta-tyrosine and of its metabolites
Konkel, Jamie T,Fan, Junfa,Jayachandran,Kirk, Kenneth L
, p. 27 - 32 (2007/10/03)
6-Fluoro-meta-tyrosine (1) was prepared from 2-fluoro-5-hydroxybenzaldehyde (6) based on an Erlenmeyer-Pl?chl azlactone strategy. Products of expected metabolism of the amino acid, including 6-fluoro-meta-tyramine (2) and its O-sulfate conjugate (3), (2-f
tert-BUTYLDIMETHYLSILYL ETHERS OF PHENOLS: THEIR ONE-STEP CONVERSION TO BENZYL OR METHYL ETHERS AND UTILITY IN REGIOSELECTIVE ortho LITHIATION
Sinhababu, Achintya K.,Kawase, Masami,Borchardt, Ronald T.
, p. 4139 - 4142 (2007/10/02)
A new method for the one-step conversion of tert-butyldimethylsilyl ethers of phenols to benzyl or methyl ethers and the blocking effect of the tert-butyldimethylsilyloxy group in regioselective ortho lithiation are described.