132067-89-1Relevant articles and documents
SYNTHESIS AND TAUTOMERISM OF 1-SUBSTITUTED 3,3-DIALKYL-3,4-DIHYDROISOQUINOLINES
Aleksandrov, B. B.,Gavrilov, M. S.,Vakhrin, M. I.,Shklyaev, V. S.
, p. 662 - 665 (1985)
A number of ethyl esters of 3,3-dialkyl-3,4-dihydroisoquinoline Δ1(2H),α-α-alkylacetic acids have been synthesized.The effect of replacement of α-hydrogen by alkyl radicals on the azomethine-enamine tautomeric equilibrium was shown.
INTERACTION OF 1-METHYLTHIO-3,3-DIMETHYL-3,4-DIHYDROISOQUINOLINE WITH β-DICARBOXYLIC ACIDS, β-DICARBONYL COMPOUNDS, AND THEIR ANALOGS
Gorbunov, A. A.,Dormidontov, M. Yu.,Shklyaev, V. S.,Shklyaev, Yu. V.
, p. 1416 - 1419 (2007/10/02)
1-Methylthio-3,3-dimethyl-3,4-dihydroisoquinoline interacts as an electrophile with β-dicarbonyl compounds and their analogs to form products in which one or two hydrogen atoms of the β-carbonyl compound are replaced by a 3,3-dimethyl-3,4-dihydroisoquinolyl or 3,3-dimethyl-1,2,3,4-tetrahydroisoquinolylidene fragment.