612-76-0Relevant articles and documents
Active-alkali metal-promoted reductive cleavage of chlorinated phenols
Azzena, Ugo,Dettori, Giovanna,Pisano, Luisa,Pittalis, Mario,Mangano, Giuseppe,Petretto, Giacomo,Pintore, Giorgio
experimental part, p. 601 - 605 (2012/07/28)
We investigated the degradation of chlorinated phenols under reductive electron transfer reaction conditions. Although Li and Na metal proved useless, activated forms of these metals, either their soluble naphthalene radical anions or 1,2-diarylethane dianions, promoted the degradation of the starting materials to various extents. Additionally, efficient dehalogenation of the sodium salts of several mono-, di-, and tri-chlorophenols was obtained by their reduction with an excess of Na metal and a catalytic amount of naphthalene. Springer-Verlag 2012.
Synthesis of 1-Propyl-3-(3-hydroxyphenyl)piperidine by Regiocontrolled Palladium-Catalyzed Arylation
Nilsson, Kristina,Hallberg, Anders
, p. 4015 - 4017 (2007/10/02)
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2-amino (or hydroxy) phenethyl-1,2,3,4-tetrahydroisoquinolines as analgesics
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, (2008/06/13)
Analgesic 1,2,3,4-tetrahydroisoquinolines of the formula (1) STR1 wherein R1 and R2 respectively are hydrogen, hydroxy or alkoxy of 1 to 4 carbon atoms, R3 and R4 respectively are hydrogen or alkyl of 1 to 4 car