121251-86-3Relevant articles and documents
Synthesis and β-adrenergic activity of atypical β-adrenergic phenylethanolaminotetralin stereoisomers
Cecchi, R.,Croci, T.,Boigegrain, R.,Boveri, S.,Baroni, M.,et al.
, p. 259 - 268 (2007/10/02)
A series of substituted phenylethanolaminotetralins were synthesized as pure stereoisomers and their ability to stimulate atypical β-adrenoceptors selectively was evaluated.The compounds in vitro relative potencies were assessed using the atypical β respo
Process for the O-alkylation of N-(hydroxy)aralkylphenylethanolamines
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, (2008/06/13)
A process for the preparation of a compound of formula STR1 wherein X represents hydrogen, halogen, trifluoromethyl or lower alkyl group; W represents methyl, Q represents hydrogen or W and Q, together, form an ethylene group and R' represents a lower alkyl group which comprises protecting the amino group of the phenol corresponding to the compound of formula I, submitting the compound thus obtained to an alkylation (with a compound of formula Hal--CH2 --COOR', wherein R' is as defined hereinabove for the formula I and Hal is chlorine, bromine or iodine) and then releasing the amino group of the product thus obtained.