145122-34-5Relevant articles and documents
Enantioselective synthesis of 1-substituted tetrahydroisoquinoline-1-carboxylic acids
Czarnocki, Zbigniew,Suh, Dennis,MacLean, David B.,Hultin, Philip G.,Szarek, Walter A.
, p. 1555 - 1561 (2007/10/02)
The 3,4-dihydroisoquinolinium salt 1 and its enantiomer have been converted readily and stereoselectively into (+)- and (-)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-methylisoquinoline-1-carboxylic acids.The synthetic route described should be applicable to the enantioselective synthesis of a variety of 1-alkyl- or 1-aryl-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acids.The absolute configuration of the amino acid hydrochloride 11 was established to be as depicted in scheme 2.