Asymmetric acyl-Strecker reaction promoted by novel thiourea organocatalyst was written by Kanemitsu, Takuya;Toyoshima, Eisuke;Miyazaki, Michiko;Nagata, Kazuhiro;Itoh, Takashi. And the article was included in Heterocycles in 2010.HPLC of Formula: 3382-18-1 This article mentions the following:
An asym. acyl-Strecker reaction using a novel thiourea organocatalyst was described. Screening experiments of the catalysts revealed that a bifunctional organocatalyst afforded an enantio-enriched product via an unique mechanism. That is, dihydroisoquinolines were converted to a corresponding 1-cyano-1,2,3,4-tetrahydroisoquinolines using the bifunctional thiourea catalyst derived from Betti base in moderate yield and enantioselectivity. In the experiment, the researchers used many compounds, for example, 6,7-Dimethoxy-3,4-dihydroisoquinoline (cas: 3382-18-1HPLC of Formula: 3382-18-1).
6,7-Dimethoxy-3,4-dihydroisoquinoline (cas: 3382-18-1) belongs to isoquinoline derivatives. Isoquinoline is a structural isomer of quinoline, which have antiseptic, antipyretic and anti-cyclic properties, and can be used as antimalarial drugs and for the preparation of other antimalarial medicine. Other industrial applications include their use as corrosion inhibitors, preservatives, and as solvents for resins and terpenes.HPLC of Formula: 3382-18-1
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem